Publication – Analytical Chemistry, Ozawa Lab Department of Chemistry, School of Science, The University of Tokyo

Refereed Papers

2024

Optical control of nanobody-mediated protein activity modulation with photocleavable fluorescent protein.
M. Endo, S. Tomizawa, Q. Kuang and T. Ozawa,
Analyst, 149, 3865-3870 (2024). doi: 10.1039/D4AN00433G
Bio-Chemoinformatics-Driven Analysis of nsp7 and nsp8 Mutations and Their Effects on Viral Replication Protein Complex Stability.
B. J. J. Subong and T. Ozawa,
Curr. Issues Mol. Biol., 46, 2598-2619 (2024). doi.org/10.3390/cimb46030165

2023

Split Luciferase-Fragment Reconstitution for Unveiling RNA Localization and Dynamics in Live Cells.
M. Eguchi, H. Yoshimura, Y. Ueda and T. Ozawa,
ACS Sensors, 8(11), 4055-4063 (2023). DOI: 10.1021/acssensors.3c01080
Lactate biosensors for spectrally and spatially multiplexed fluorescence imaging.
Y. Nasu, A. Aggarwal, G. Le, C. Vo, Y. Kambe, X. Wang, F. Beinlich, A. Lee, T. Ram, F. Wang, K. Gorzo, Y. Kamijo, M. Boisvert, S. Nishinami, G. Kawamura, T. Ozawa, H. Toda, G. Gordon, S. Ge, H. Hirase, M. Nedergaard, M.-E. Paquet, M. Drobizhev, K. Podgorski, and R. Campbell,
Nature Communications, 14, 6598 (2023). DOI: 10.1038/s41467-023-42230-5
Protocol for screening cellular outputs activated by optogenetically-controlled temporal PI3K signaling activation patterns.
Y. Ueda, S. Matsushita, M. Suzuki, T. Ozawa,
STAR Protocols, 4, 102622 (2023). DOI: 10.1016/j.xpro.2023.102622.
Class 3 PI3K participates in nuclear gene transcription and co-activates the circadian clock to promote de novo purine synthesis. C. Alkhoury,
N. Henneman, V. Petrenko, Y. Shibayama, A. Segaloni, A. Gadault, I. Nemazanyy, E.L. Guillou, A. D. Wolide, K. Antoniadou, X. Tong, T. Tamaru, T. Ozawa, M. Girard, K. Hnia, D. Lutter, C. Dibner and G. Panasyuk,
Nature Cell Biology, 25, 975-988 (2023). DOI: 10.1038/s41556-023-01171-3.
Optogenetic decoding of Akt2-regulated cellular metabolic signaling pathways in skeletal muscle cells using transomics analysis.
G. Kawamura, T. Kokaji, K. Kawata, Y. Sekine, Y. Suzuki, T. Soga, Y. Ueda, M. Endo, S. Kuroda and T. Ozawa,
Science Signaling, 16, eabn0782 (2023). DOI: 10.1126/scisignal.abn0782
RNA Aptamer-Based Approach to Inhibiting Split-GFP Reconstruction and the Loss of Inhibitory Activity Using Complementary RNA.
T. Kamura, Y. Katsuda, Y. Fuchigami, Y. Itsuki, Y. Kitamura, T. Sakurai, T. Ozawa and T. Ihara,
Bulletin of Chemistry Society Japan, 96, 241-246 (2023). DOI: 10.1246/bcsj.20220331
Akaike’s Information Criterion for Stoichiometry Inference of Supramolecular Complexes.
K. Ikemoto, K. Takahashi, T. Ozawa, H. Isobe,
Angewandte Chemie Int. Ed., 62, e202219059 (2023). DOI: org/10.1002/anie.202219059

2022

Imaging and manipulation of plasma membrane fatty acids clusters using TOF-SIMS combined optogenetics.
C. Zhang, K. Kikushima, M. Endo, T. Kahyo, M. Horikawa, T. Matsudaira, T. Tanaka, Y. Takanashi, T. Sato, Y. Takahashi, L. Xu, N. Takayama, A. Islam, M. A. Mamun, T. Ozawa and M Setou,
Cells, 12, 10 (2022). DOI: 10.3390/cells12010010.
Blue light alters cellular lipidome–Light-induced lipidomic changes can be modulated by optogenetically engineered cPLA2α.
C. Zhang, L. Xu, M. Endo, T. Kahyo, K. Kikushima, M. Horikawa, M. Murakami, A.S.M. Waliullah, M. M. Hasan, T. Sakamoto, Y. Takahashi, S. Aramaki, T. Ozawa and M. Setou,
Journal of Photochemistry Photobiology, 12, 100150 (2022). DOI: 10.1016/j.jpap.2022.100150
Mechanistic insights into cancer drug resistance through optogenetic PI3K signaling hyperactivation.
Y. Ueda, Y. Miura, N. Tomishige, N. Sugimoto, M. Murase, G. Kawamura, N. Sasaki, T. Ishiwata, and T. Ozawa,
Cell Chemical Biology 29, 1576-1587 (2022). DOI: 10.1016/j.chemBiology2022.10.002.
Systematic Interrogation of the Temperature Perturbation in the Insulin Signaling Pathway for Optogenetic Stimulation.
Q. Dong, M. Endo, G. Kawamura and T. Ozawa,
Cells, 11, 3136 (2022). DOI: 10.3390/cells11193136.
Increased spine PIP₃ is sequestered from dendritic shafts.
Y. Ueda, N. Sugimoto and T. Ozawa,
Molecular Brain, 15, 59 (2022). DOI: 10.1186/s13041-022-00944-5.
N-Heterocyclic carbene-based C-centered Au(I)-Ag(I) clusters with intense phosphorescence and the ligand-specific, organelle-selective translocation in cells.
Z. Lei, M. Endo, H. Ube, T. Shiraogawa, P. Zhao, K. Nagata, X.-L. Pei, T. Eguchi, T. Kamachi, M. Ehara*, T. Ozawa* and M. Shionoya*,
Nature Communication, 13, 4288 (2022). DOI: 10.1038/s41467-022-31891-3
Discovery of a Phase-Separating Small Molecule That Selectively Sequesters Tubulin in Cells.
G. Ado, N. Noda, H. T. Vu, A. Perron, A. D. Mahapatra, K. P. Arista, H. Yoshimura, D. M. Packwood, F. Ishidate, S. Sato, T. Ozawa and M. Uesugi,
Chemical Science, 13, 5760-5766 (2022). DOI: 10.1039/d1sc07151c.
Sphingomyelin localization in the intestinal crypt surface.
M. Ueda, M. Abe, T. Ishiwata and T. Ozawa,
Biochemical and Biophysical Research Communications, 611, 14-18 (2022). DOI: 10.1016/j.bbrc.2022.03.128
Castanospermine suppresses CD44 ectodomain cleavage as revealed by transmembrane bioluminescent sensors.
N. Noda and T. Ozawa,
Journal of Cell Science, 135, jcs259314 (2022). DOI: 10.1242/jcs.259314
A Series of Furimazine Derivatives for Sustained Live-cell Bioluminescence Imaging and Application to the Monitoring of Myogenesis at Single-cell Level.
M. Orioka, M. Eguchi, Y. Mizui, Y. Ikeda, A. Sakama, Q. Li, H. Yoshimura, T. Ozawa, D. Citterio, and Y. Hiruta,
Bioconjugate Chemistry, 33, 496-504 (2022). DOI: 10.1021/acs.bioconjChemistry2c00035.
Poly(ADP-ribose) polymerase (PARP) is critically involved in liver ischemia/reperfusion-injury.
S. Haga, A. Kanno, N. Morita, S. Jin, K. Matoba, T. Ozawa and M. Ozaki,
Journal of Surgical Research, 270,124-138 (2022). DOI: 10.1016/j.jss.2021.09.008

2021

Synergetic roles of Formyl Peptide Receptor 1 oligomerization in ligand-induced signal transduction.
T. Nishiguchi, H. Yoshimura, R.S. Kasai, T.K. Fujiwara and T. Ozawa,
ACS Chemistry Biology, 18, 2577-2587 (2020). DOI: 10.1021/acschembio.0c00631.
Fluorescent H₂ Receptor Squaramide-Type Antagonists: Synthesis, Characterization, and Applications.
S. Biselli, I. Alencastre, K. Tropmann, D. Erdmann, M. Chen, T. Littmann, A. F. Maia, M. Gomez-Lazaro, M. Tanaka, T. Ozawa, M. Keller, M. Lamghari, A. Buschauer, G. Bernhardt,
ACS Medicinal Chemistry Letters, 11, 1521-1528 (2020). DOI: 10.1021/acsmedchemlett.0c00033.

2020

S. Biselli, I. Alencastre, K. Tropmann, D. Erdmann, M. Chen, T. Littmann, A. F. Maia, M. Gomez-Lazaro, M. Tanaka, T. Ozawa, M. Keller, M. Lamghari, A. Buschauer, G. Bernhardt, Fluorescent H ₂ Receptor Squaramide-Type Antagonists: Synthesis, Characterization, and Applications. ACS Medicinal Chemistry Letters. 11, 1521–1528 (2020).
DOI:10.1021/acsmedchemlett.0c00033
T. Nishiguchi, H. Yoshimura, R. S. Kasai, T. K. Fujiwara, T. Ozawa, Synergetic roles of Formyl Peptide Receptor 1 oligomerization in ligand-induced signal transduction. ACS Chemical Biology. 15, 2577–2587 (2020).
DOI:10.1021/acschembio.0c00631

2019

Parallelized shifted‐excitation Raman difference spectroscopy for fluorescence rejection in a temporary varying system.
R. Shimada, T. Nakamura, T. Ozawa,
Journal of Biophotonics. 12, e201960028 (2019). DOI:10.1002/jbio.201960028
Comprehensive modeling of bloodstain aging by multivariate Raman spectral resolution with kinetics.
A. Takamura, D. Watanabe, R. Shimada, T. Ozawa,
Communications Chemistry. 2, 115 (2019). DOI:10.1038/s42004-019-0217-1
Enhanced bioluminescent sensor for longitudinal detection of CREB activation in living cells.
N. Noda, T. Ishimoto, H. Mori, T. Ozawa,
Photochemical & Photobiological Sciences. 18, 2740–2747 (2019). DOI:10.1039/C9PP00249A.
Photocleavable Cadherin Inhibits Cell-to-Cell Mechanotransduction by Light.
M. Endo, T. Iwawaki, H. Yoshimura, T. Ozawa,
ACS Chemical Biology. 14, 2206–2214 (2019). DOI:10.1021/acschembio.9b00460.
A. Buschauer, G. Bernhardt, [ 3 H]UR-DEBa176: A 2,4-Diaminopyrimidine-Type Radioligand Enabling Binding Studies at the Human, Mouse, and Rat Histamine H 4 Receptors.
E. Bartole, T. Littmann, M. Tanaka, T. Ozawa,
Journal of Medicinal Chemistry. 62, 8338–8356 (2019). DOI:10.1021/acs.jmedchem.9b01342
M. ENDO, M. MIYASAKI, Q. LI, G. KAWAMURA, T. OZAWA,
A Detection Method for GLUT4 Exocytosis Based on Spontaneous Split Luciferase Complementation.
Analytical Sciences. 35, 835–838 (2019). DOI:10.2116/analsci.19C003
Phenotype Profiling for Forensic Purposes: Determining Donor Sex Based on Fourier Transform Infrared Spectroscopy of Urine Traces.
A. Takamura, L. Halamkova, T. Ozawa, I. K. Lednev,
Analytical Chemistry. 91, 6288–6295 (2019). DOI:10.1021/acs.analchem.9b01058
Using redox-sensitive mitochondrial cytochrome Raman bands for label-free detection of mitochondrial dysfunction.
T. Morimoto, L. Chiu, H. Kanda, H. Kawagoe, T. Ozawa, M. Nakamura, K. Nishida, K. Fujita, T. Fujikado,
The Analyst. 144, 2531–2540 (2019). DOI:10.1039/C8AN02213E PubMed:30839952
Activation of caspase-3 during Chlamydia trachomatis -induced apoptosis at a late stage.
J. Matsuo, S. Haga, K. Hashimoto, T. Okubo, T. Ozawa, M. Ozaki, H. Yamaguchi,
Canadian Journal of Microbiology. 65, 135–143 (2019). DOI:10.1139/cjm-2018-0408

2018

Unique Roles of β-Arrestin in GPCR Trafficking Revealed by Photoinducible Dimerizers.
O. Takenouchi, H. Yoshimura, T. Ozawa,
Scientific Reports. 8, 677 (2018). DOI:10.1038/s41598-017-19130-y
Cooperative interaction among BMAL1, HSF1, and p53 protects mammalian cells from UV stress.
G. Kawamura, M. Hattori, K. Takamatsu, T. Tsukada, Y. Ninomiya, I. Benjamin, P. Sassone-Corsi, T. Ozawa, T. Tamaru,
Communications Biology. 1, 204 (2018). DOI:10.1038/s42003-018-0209-1
Soft and Robust Identification of Body Fluid Using Fourier Transform Infrared Spectroscopy and Chemometric Strategies for Forensic Analysis.
A. Takamura, K. Watanabe, T. Akutsu, T. Ozawa,
Scientific Reports. 8, 8459 (2018). DOI:10.1038/s41598-018-26873-9
Preferential Photoreaction in a Porous Crystal, Metal–Macrocycle Framework: Pd II -Mediated Olefin Migration over [2+2] Cycloaddition.
H. Yonezawa, S. Tashiro, T. Shiraogawa, M. Ehara, R. Shimada, T. Ozawa, M. Shionoya,
Journal of the American Chemical Society. 140, 16610–16614 (2018). DOI:10.1021/jacs.8b08534
A split luciferase-based probe for quantitative proximal determination of Gαq signalling in live cells.
T. Littmann, T. Ozawa, C. Hoffmann, A. Buschauer, G. Bernhardt,
Scientific Reports. 8, 17179 (2018). DOI:10.1038/s41598-018-35615-w
Light-controllable Transcription System by Nucleocytoplasmic Shuttling of a Truncated Phytochrome B.
N. Noda, T. Ozawa,
Photochemistry and Photobiology. 94, 1071–1076 (2018). DOI:10.1111/php.12955
A robust split-luciferase-based cell fusion screening for discovering myogenesis-promoting molecules.
Q. Li, H. Yoshimura, M. Komiya, K. Tajiri, M. Uesugi, Y. Hata, T. Ozawa,
The Analyst. 143, 3472–3480 (2018). DOI:10.1039/C8AN00285A
Establishing a Split Luciferase Assay for Proteinkinase G (PKG) Interaction Studies.
A. Schramm, P. Mueller-Thuemen, T. Littmann, M. Harloff, T. Ozawa, J. Schlossmann,
International Journal of Molecular Sciences. 19, 1180 (2018). DOI:10.3390/ijms19041180
Detection of Necroptosis in Ligand-Mediated and Hypoxia-Induced Injury of Hepatocytes Using a Novel Optic Probe-Detecting Receptor-Interacting Protein (RIP)1/RIP3 Binding.
S. Haga, A. Kanno, T. Ozawa, N. Morita, M. Asano, M. Ozaki,
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics. 26, 503–513 (2018). DOI:10.3727/096504017X15005102445191
Photo-Activatable Akt Probe: A New Tool to Study the Akt-Dependent Physiopathology of Cancer Cells.
S. Haga, T. Ozawa, N. Morita, M. Asano, S. Jin, Yimin, M. Ozaki,
Oncology Research Featuring Preclinical and Clinical Cancer Therapeutics. 26, 467–472 (2018). DOI:10.3727/096504017X15040166233313

2017

Optogenetic interrogation reveals separable G-protein-dependent and -independent signalling linking G-protein-coupled receptors to the circadian oscillator.
H. J. Bailes, N. Milosavljevic, L.-Y. Zhuang, E. J. Gerrard, T. Nishiguchi, T. Ozawa, R. J. Lucas,
BMC Biology. 15, 40 (2017). DOI:10.1186/s12915-017-0380-8
Dynamic monitoring of p53 translocation to mitochondria for the analysis of specific inhibitors using luciferase-fragment complementation.
N. Noda, R. Awais, R. Sutton, M. Awais, T. Ozawa,
Biotechnology and Bioengineering. 114, 2818–2827 (2017). DOI:10.1002/bit.26407
A genetic screen to discover SUMOylated proteins in living mammalian cells.
M. Komiya, A. Ito, M. Endo, D. Hiruma, M. Hattori, H. Saitoh, M. Yoshida, T. Ozawa,
Scientific Reports. 7, 17443 (2017). DOI:10.1038/s41598-017-17450-7
Rapid in vivo lipid/carbohydrate quantification of single microalgal cell by Raman spectral imaging to reveal salinity-induced starch-to-lipid shift.
Biotechnology for Biofuels. 10, 9 (2017). DOI:10.1186/s13068-016-0691-y
Spectral Mining for Discriminating Blood Origins in the Presence of Substrate Interference via Attenuated Total Reflection Fourier Transform Infrared Spectroscopy: Postmortem or Antemortem Blood?
A. Takamura, K. Watanabe, T. Akutsu, H. Ikegaya, T. Ozawa,
Analytical Chemistry. 89, 9797–9804 (2017). DOI:10.1021/acs.analchem.7b01756
In Search of NPY Y 4 R Antagonists: Incorporation of Carbamoylated Arginine, Aza-Amino Acids, or d -Amino Acids into Oligopeptides Derived from the C-Termini of the Endogenous Agonists.
K. K. Kuhn, T. Littmann, S. Dukorn, M. Tanaka, M. Keller, T. Ozawa, G. Bernhardt, A. Buschauer,
ACS Omega. 2, 3616–3631 (2017). DOI:10.1021/acsomega.7b00451
Liquid/Liquid Interfacial Synthesis of a Click Nanosheet.
A. Rapakousiou, R. Sakamoto, R. Shiotsuki, R. Matsuoka, U. Nakajima, T. Pal, R. Shimada, A. Hossain, H. Masunaga, S. Horike, Y. Kitagawa, S. Sasaki, K. Kato, T. Ozawa, D. Astruc, H. Nishihara,
Chemistry – A European Journal. 23, 8443–8449 (2017). DOI:10.1002/chem.201700201
Split luciferase complementation assay for the analysis of G protein-coupled receptor ligand response in Saccharomyces cerevisiae.
Y. Fukutani, J. Ishii, A. Kondo, T. Ozawa, H. Matsunami, M. Yohda,
Biotechnology and Bioengineering. 114, 1354–1361 (2017). DOI:10.1002/bit.26255
Single-shot phase-shifting incoherent digital holography.
T. Tahara, T. Kanno, Y. Arai, T. Ozawa,
Journal of Optics. 19, 065705 (2017). DOI:10.1088/2040-8986/aa6e82
Protein expression guided chemical profiling of living cells by the simultaneous observation of Raman scattering and anti-Stokes fluorescence emission.
L. Chiu, T. Ichimura, T. Sekiya, H. Machiyama, T. Watanabe, H. Fujita, T. Ozawa, K. Fujita,
Scientific Reports. 7, 43569 (2017). DOI:10.1038/srep43569

2016

Attenuation of chemokine receptor function and surface expression as an immunomodulatory strategy employed by human cytomegalovirus is linked to vGPCR US28.
T. Frank, A. Reichel, O. Larsen, A.-C. Stilp, M. M. Rosenkilde, T. Stamminger, T. Ozawa, N. Tschammer,
Cell Communication and Signaling. 14, 31 (2016). DOI:10.1186/s12964-016-0154-x
Label-free versus conventional cellular assays: Functional investigations on the human histamine H1 receptor.
S. Lieb, T. Littmann, N. Plank, J. Felixberger, M. Tanaka, T. Schäfer, S. Krief, S. Elz, K. Friedland, G. Bernhardt, J. Wegener, T. Ozawa, A. Buschauer,
Pharmacological Research. 114, 13–26 (2016). DOI:10.1016/j.phrs.2016.10.010
Spatiotemporal analysis with a genetically encoded fluorescent RNA probe reveals TERRA function around telomeres.
T. Yamada, H. Yoshimura, R. Shimada, M. Hattori, M. Eguchi, T. K. Fujiwara, A. Kusumi, T. Ozawa,
Scientific Reports. 6, 38910 (2016). DOI:10.1038/srep38910
Bioluminescent Indicator for Highly Sensitive Analysis of Estrogenic Activity in a Cell-Based Format.
O. Takenouchi, A. Kanno, H. Takakura, M. Hattori, T. Ozawa,
Bioconjugate Chemistry. 27, 2689–2694 (2016). DOI:10.1021/acs.bioconjchem.6b00466
Optogenetic activation of axon guidance receptors controls direction of neurite outgrowth.
M. Endo, M. Hattori, H. Toriyabe, H. Ohno, H. Kamiguchi, Y. Iino, T. Ozawa,
Scientific Reports. 6, 23976 (2016). DOI:10.1038/srep23976
In Situ Characterization of Bak Clusters Responsible for Cell Death Using Single Molecule Localization Microscopy.
Y. Nasu, A. Benke, S. Arakawa, G. J. Yoshida, G. Kawamura, S. Manley, S. Shimizu, T. Ozawa,
Scientific Reports. 6, 27505 (2016). DOI:10.1038/srep27505
Confocal Bioluminescence Imaging for Living Tissues with a Caged Substrate of Luciferin.
M. Hattori, G. Kawamura, R. Kojima, M. Kamiya, Y. Urano, T. Ozawa,
Analytical Chemistry. 88, 6231–6238 (2016). DOI:10.1021/acs.analchem.5b04142
Genetically Encoded Fluorescent Probe for Imaging Apoptosis in Vivo with Spontaneous GFP Complementation.
Y. Nasu, Y. Asaoka, M. Namae, H. Nishina, H. Yoshimura, T. Ozawa,
Analytical Chemistry. 88, 838–844 (2016). DOI:10.1021/acs.analchem.5b03367

2015

An optogenetic system for interrogating the temporal dynamics of Akt.
Y. Katsura, H. Kubota, K. Kunida, A. Kanno, S. Kuroda, T. Ozawa,
Scientific Reports. 5, 14589 (2015). DOI:10.1038/srep14589
CRY Drives Cyclic CK2-Mediated BMAL1 Phosphorylation to Control the Mammalian Circadian Clock.
T. Tamaru, M. Hattori, K. Honda, Y. Nakahata, P. Sassone-Corsi, G. T. J. van der Horst, T. Ozawa, K. Takamatsu,
PLOS Biology. 13, e1002293 (2015). DOI:10.1371/journal.pbio.1002293
Recruitment of β -Arrestin 1 and 2 to the β 2 -Adrenoceptor: Analysis of 65 Ligands. T. Littmann, M. Göttle, M. T. Reinartz, S. Kälble, I. W. Wainer, T. Ozawa, R. Seifert,
Journal of Pharmacology and Experimental Therapeutics. 355, 183–190 (2015). DOI:10.1124/jpet.115.227959
Multimodal and multiplex spectral imaging of rat cornea ex vivo using a white-light laser source.
H. Segawa, Y. Kaji, P. Leproux, V. Couderc, T. Ozawa, T. Oshika, H. Kano,
Journal of Biophotonics. 8, 705–713 (2015). DOI:10.1002/jbio.201400059
A new cell-based assay to evaluate myogenesis in mouse myoblast C2C12 cells.
M. Kodaka, Z. Yang, K. Nakagawa, J. Maruyama, X. Xu, A. Sarkar, A. Ichimura, Y. Nasu, T. Ozawa, H. Iwasa, M. Ishigami-Yuasa, S. Ito, H. Kagechika, Y. Hata,
Experimental Cell Research. 336, 171–181 (2015). DOI:10.1016/j.yexcr.2015.06.015
Development of red-shifted mutants derived from luciferase of Brazilian click beetle Pyrearinus termitilluminans.
T. Nishiguchi, T. Yamada, Y. Nasu, M. Ito, H. Yoshimura, T. Ozawa,
Journal of Biomedical Optics. 20, 101205 (2015). DOI:10.1117/1.JBO.20.10.101205
Multimodal Imaging of Living Cells with Multiplex Coherent Anti-stokes Raman Scattering (CARS), Third-order Sum Frequency Generation (TSFG) and Two-photon Excitation Fluorescence (TPEF) Using a Nanosecond White-light Laser Source.
H. SEGAWA, M. OKUNO, P. LEPROUX, V. COUDERC, T. OZAWA, H. KANO,
Analytical Sciences. 31, 299–305 (2015). DOI:10.2116/analsci.31.299
High-throughput Live Cell Imaging and Analysis for Temporal Reaction of G Protein-coupled Receptor Based on Split Luciferase Fragment Complementation.
M. HATTORI, T. OZAWA,
Analytical Sciences. 31, 327–330 (2015). DOI:10.2116/analsci.31.327
Simultaneous Time-Lamination Imaging of Protein Association Using a Split Fluorescent Timer Protein.
A. Takamura, M. Hattori, H. Yoshimura, T. Ozawa,
Analytical Chemistry. 87, 3366–3372 (2015). DOI:10.1021/ac504583t
Structure-bias relationships for fenoterol stereoisomers in six molecular and cellular assays at the β2-adrenoceptor.
M. T. Reinartz, S. Kälble, T. Littmann, T. Ozawa, S. Dove, V. Kaever, I. W. Wainer, R. Seifert,
Naunyn-Schmiedeberg’s Archives of Pharmacology. 388, 51–65 (2015). DOI:10.1007/s00210-014-1054-5

2014

p62/SQSTM1 Plays a Protective Role in Oxidative Injury of Steatotic Liver in a Mouse Hepatectomy Model.
S. Haga, T. Ozawa, Y. Yamada, N. Morita, I. Nagashima, H. Inoue, Y. Inaba, N. Noda, R. Abe, K. Umezawa, M. Ozaki,
Antioxidants & Redox Signaling. 21, 2515–2530 (2014). DOI:10.1089/ars.2013.5391
Developing a potentially immunologically inert tetracycline-regulatable viral vector for gene therapy in the peripheral nerve.
S. A. Hoyng, S. Gnavi, F. de Winter, R. Eggers, T. Ozawa, A. Zaldumbide, R. C. Hoeben, J. A. M Malessy, J. Verhaagen,
Gene Therapy. 21, 549–557 (2014). DOI:10.1038/gt.2014.22
Electronically resonant third-order sum frequency generation spectroscopy using a nanosecond white-light supercontinuum.
H. Segawa, N. Fukutake, P. Leproux, V. Couderc, T. Ozawa, H. Kano,
Optics Express. 22, 10416 (2014). DOI:10.1364/OE.22.010416
Long Noncoding RNA NEAT1-Dependent SFPQ Relocation from Promoter Region to Paraspeckle Mediates IL8 Expression upon Immune Stimuli.
K. Imamura, N. Imamachi, G. Akizuki, M. Kumakura, A. Kawaguchi, K. Nagata, A. Kato, Y. Kawaguchi, H. Sato, M. Yoneda, C. Kai, T. Yada, Y. Suzuki, T. Yamada, T. Ozawa, K. Kaneki, T. Inoue, M. Kobayashi, T. Kodama, Y. Wada, K. Sekimizu, N. Akimitsu,
Molecular Cell 53, 393–406 (2014) DOI: 10.1016/j.molcel.2014.01.009.
Assay methods for small ubiquitin-like modifier (SUMO)–SUMO-interacting motif (SIM) interactions in vivo and in vitro using a split-luciferase complementation system.
M. Hirohama, A. R. D. Voet, T. Ozawa, H. Saitoh, Y. Nakao, K. Y. J. Zhang, A. Ito, M. Yoshida, Analytical Biochemistry. 448, 92–94 (2014). DOI:10.1016/j.ab.2013.12.009

2013

Bioluminescent Probes to Analyze Ligand-Induced Phosphatidylinositol 3,4,5-Trisphosphate Production with Split Luciferase Complementation. L. Yang, Y. Nasu, M. Hattori, H. Yoshimura, A. Kanno, T. Ozawa,
Analytical Chemistry. 85, 11352–11359 (2013). DOI:10.1021/ac402278f
Spatiotemporal visualization of proHB-EGF ectodomain shedding in living cells.
H. Inoue, T. Sakaue, T. Ozawa, S. Higashiyama,
The Journal of Biochemistry. 154, 67–76 (2013). DOI:10.1093/jb/mvt030
Longitudinal Bioluminescence Imaging of the Dynamics of Doxorubicin Induced Apoptosis.
G. Niu, L. Zhu, D. N. Ho, F. Zhang, H. Gao, Q. Quan, N. Hida, T. Ozawa, G. Liu, X. Chen,
Theranostics. 3, 190–200 (2013). DOI:10.7150/thno.5825
ROS Stress Resets Circadian Clocks to Coordinate Pro-Survival Signals.
T. Tamaru, M. Hattori, Y. Ninomiya, G. Kawamura, G. Varès, K. Honda, D. P. Mishra, B. Wang, I. Benjamin, P. Sassone-Corsi, T. Ozawa, K. Takamatsu,
PLoS ONE. 8, e82006 (2013). DOI:10.1371/journal.pone.0082006
Folding Coupled with Assembly in Split Green Fluorescent Proteins Studied by Structure-based Molecular Simulations.
M. Ito, T. Ozawa, S. Takada,
The Journal of Physical Chemistry B. 117, 13212–13218 (2013). DOI:10.1021/jp4032817
Sustained accurate recording of intracellular acidification in living tissues with a photo-controllable bioluminescent protein.
M. Hattori, S. Haga, H. Takakura, M. Ozaki, T. Ozawa,
Proceedings of the National Academy of Sciences of USA. 110, 9332–9337 (2013). DOI:10.1073/pnas.1304056110
Rational Design and Development of Near-Infrared-Emitting Firefly Luciferins Available In Vivo.
R. Kojima, H. Takakura, T. Ozawa, Y. Tada, T. Nagano, Y. Urano,
Angewandte Chemie International Edition. 52, 1175–1179 (2013). DOI:10.1002/anie.201205151
Analysis of temporal patterns of GPCR–β-arrestin interactions using split luciferase-fragment complementation.
M. Hattori, M. Tanaka, H. Takakura, K. Aoki, K. Miura, T. Anzai, T. Ozawa,
Molecular BioSystems. 9, 957 (2013). DOI:10.1039/c2mb25443c

2012

In Vivo Monitoring of Liver Damage Using Caspase-3 Probe.
M. Ozaki, S. Haga, T. Ozawa,
Theranostics. 2, 207–214 (2012). DOI:10.7150/thno.3806
Development of 5′- and 7′-Substituted Luciferin Analogues as Acid-Tolerant Substrates of Firefly Luciferase.
H. Takakura, R. Kojima, T. Ozawa, T. Nagano, Y. Urano,
ChemBioChem. 13, 1424–1427 (2012). DOI:10.1002/cbic.201200142
Fluorescent Probes for Imaging Endogenous β-Actin mRNA in Living Cells Using Fluorescent Protein-Tagged Pumilio.
H. Yoshimura, A. Inaguma, T. Yamada, T. Ozawa,
ACS Chemical Biology. 7, 999–1005 (2012). DOI:10.1021/cb200474a
Measuring CREB Activation Using Bioluminescent Probes That Detect KID–KIX Interaction in Living Cells.
T. Ishimoto, H. Mano, T. Ozawa, H. Mori,
Bioconjugate Chemistry. 23, 923–932 (2012). DOI:10.1021/bc200491j
Visualization and Quantitative Analysis of G Protein-Coupled Receptor−β-Arrestin Interaction in Single Cells and Specific Organs of Living Mice Using Split Luciferase Complementation.
H. Takakura, M. Hattori, M. Takeuchi, T. Ozawa,
ACS Chemical Biology. 7, 901–910 (2012). DOI:10.1021/cb200360z

2011

Synchronization of Circadian Per2 Rhythms and HSF1-BMAL1:CLOCK Interaction in Mouse Fibroblasts after Short-Term Heat Shock Pulse.
T. Tamaru, M. Hattori, K. Honda, I. Benjamin, T. Ozawa, K. Takamatsu,
PLoS ONE. 6, e24521 (2011). DOI:10.1371/journal.pone.0024521
Visualization of Nonengineered Single mRNAs in Living Cells Using Genetically Encoded Fluorescent Probes.
T. Yamada, H. Yoshimura, A. Inaguma, T. Ozawa,
Analytical Chemistry. 83, 5708–5714 (2011). DOI:10.1021/ac2009405
Real-Time Monitoring of Actin Polymerization in Living Cells Using Split Luciferase. T. Ishimoto, T. Ozawa, H. Mori,
Bioconjugate Chemistry. 22, 1136–1144 (2011). DOI:10.1021/bc100595z
Dual-Color Bioluminescence Analysis for Quantitatively Monitoring G-Protein-Coupled Receptor and β-Arrestin Interactions.
A. K. M. Kafi, M. Hattori, N. Misawa, T. Ozawa,
Pharmaceuticals. 4, 457–469 (2011). DOI:10.3390/ph4030457

2010 and before

p66Shc has a pivotal function in impaired liver regeneration in aged mice by a redox-dependent mechanism.
S. Haga, N. Morita, K. Irani, M. Fujiyoshi, T. Ogino, T. Ozawa, M. Ozaki,
Laboratory Investigation. 90, 1718–1726 (2010).
DOI:10.1038/labinvest.2010.119
Ratiometric Bioluminescence Indicators for Monitoring Cyclic Adenosine 3′,5′-Monophosphate in Live Cells Based on Luciferase-Fragment Complementation.
M. Takeuchi, Y. Nagaoka, T. Yamada, H. Takakura, T. Ozawa,
Analytical Chemistry. 82, 9306–9313 (2010).
DOI:10.1021/ac102692u
S. B. Kim, T. Ozawa, Creating bioluminescent indicators to visualise biological events in living cells and animals. Supramolecular Chemistry. 22, 440–449 (2010).
DOI:10.1080/10610278.2010.485251
Rapid and High-Sensitivity Cell-Based Assays of Protein−Protein Interactions Using Split Click Beetle Luciferase Complementation: An Approach to the Study of G-Protein-Coupled Receptors.
N. Misawa, A. K. M. Kafi, M. Hattori, K. Miura, K. Masuda, T. Ozawa,
Analytical Chemistry. 82, 2552–2560 (2010).
DOI:10.1021/ac100104q
LUCIFERASES FOR THE STUDY OF PROTEIN–PROTEIN INTERACTIONS IN LIVE CELLS AND ANIMALS.
A. K. M. KAFI, M. HATTORI, T. OZAWA,
Nano LIFE. 1, 79–87 (2010).
DOI:10.1142/S1793984410000079
T. Ozawa, Imaging biological molecules using novel optical probes. Photomedicine and photobiology. 31, 27–28 (2009).
High-Sensitivity Real-Time Imaging of Dual Protein-Protein Interactions in Living Subjects Using Multicolor Luciferases.
N. Hida, M. Awais, M. Takeuchi, N. Ueno, M. Tashiro, C. Takagi, T. Singh, M. Hayashi, Y. Ohmiya, T. Ozawa,
PLoS ONE. 4, e5868 (2009).
DOI:10.1371/journal.pone.0005868
Cyclic Luciferase for Real-Time Sensing of Caspase-3 Activities in Living Mammals.
A. Kanno, Y. Yamanaka, H. Hirano, Y. Umezawa, T. Ozawa,
Angewandte Chemie International Edition. 46, 7595–7599 (2007).
DOI:10.1002/anie.200700538
Nongenomic Activity of Ligands in the Association of Androgen Receptor with Src.
S. B. Kim, A. Kanno, T. Ozawa, H. Tao, Y. Umezawa,
ACS Chemical Biology. 2, 484–492 (2007).
DOI:10.1021/cb7000439
Imaging dynamics of endogenous mitochondrial RNA in single living cells.
T. Ozawa, Y. Natori, M. Sato, Y. Umezawa,
Nature Methods. 4, 413–419 (2007).
DOI:10.1038/nmeth1030
A Minimal Peptide Sequence That Targets Fluorescent and Functional Proteins into the Mitochondrial Intermembrane Space.
T. Ozawa, Y. Natori, Y. Sako, H. Kuroiwa, T. Kuroiwa, Y. Umezawa,
ACS Chemical Biology. 2, 176–186 (2007).
DOI:10.1021/cb600492a
A proinflammatory cytokine sensor cell for assaying inflammatory activities of nanoparticles.
S. B. Kim, T. Ozawa, H. Tao, Y. Umezawa,
Analytical Biochemistry. 362, 148–150 (2007).
DOI:10.1016/j.ab.2006.11.004
Methods for Imaging and Analyses of Intracellular Organelles Using Fluorescent and Luminescent Proteins.
M. TAKEUCHI, T. OZAWA,
Analytical Sciences. 23, 25–29 (2007).
DOI:10.2116/analsci.23.25
A method for determining the activities of cytokines based on the nuclear transport of nuclear factor-κB. S. B. Kim, Y. Natori, T. Ozawa, Y. Umezawa, H. Tao,
Analytical Biochemistry. 359, 147–149 (2006).
DOI:10.1016/j.ab.2006.07.013
Genetically Encoded Optical Probe for Detecting Release of Proteins from Mitochondria toward Cytosol in Living Cells and Mammals.
A. Kanno, T. Ozawa, Y. Umezawa,
Analytical Chemistry. 78, 8076–8081 (2006).
DOI:10.1021/ac061488a
Designing split reporter proteins for analytical tools.
T. Ozawa,
Analytica Chimica Acta. 556, 58–68 (2006).
DOI:10.1016/j.aca.2005.06.026
Intein-Mediated Reporter Gene Assay for Detecting Protein−Protein Interactions in Living Mammalian Cells.
A. Kanno, T. Ozawa, Y. Umezawa,
Analytical Chemistry. 78, 556–560 (2006).
DOI:10.1021/ac051451a
A genetically encoded indicator for assaying bioactive chemicals that induce nuclear transport of glucocorticoid receptor.
S. B. Kim, T. Ozawa, Y. Umezawa,
Analytical Biochemistry. 347, 213–220 (2005)
DOI:10.1016/j.ab.2005.09.011
Quantitative Determination of Protein Nuclear Transport Induced by Phosphorylation or by Proteolysis.
S. B. Kim, R. Takao, T. Ozawa, Y. Umezawa,
Analytical Chemistry. 77, 6928–6934 (2005).
DOI:10.1021/ac050966z
Genetically Encoded Stress Indicator for Noninvasively Imaging Endogenous Corticosterone in Living Mice.
S. B. Kim, T. Ozawa, Y. Umezawa,
Analytical Chemistry. 77, 6588–6593 (2005).
DOI:10.1021/ac0510078
Methods of Analysis for Protein Dynamics in Living Cells Based on Protein Splicing. T. Ozawa,
Bulletin of the Chemical Society of Japan. 78, 739–751 (2005).
DOI:10.1246/bcsj.78.739
A high-throughput screening of genes that encode proteins transported into the endoplasmic reticulum in mammalian cells.
T. Ozawa,
Nucleic Acids Research. 33, e34–e34 (2005).
DOI:10.1093/nar/gni032
High-throughput sensing and noninvasive imaging of protein nuclear transport by using reconstitution of split Renilla luciferase.
S. B. Kim, T. Ozawa, S. Watanabe, Y. Umezawa,
Proceedings of the National Academy of Sciences of the USA. 101, 11542–11547 (2004).
DOI:10.1073/pnas.0401722101
Locating a Protein−Protein Interaction in Living Cells via Split Renilla Luciferase Complementation. A. Kaihara, Y. Kawai, M. Sato, T. Ozawa, Y. Umezawa,
Analytical Chemistry. 75, 4176–4181 (2003).
DOI:10.1021/ac0300800
A Screening Method for Estrogens Using an Array-Type DNA Glass Slide.
S. B. KIM, T. OZAWA, Y. UMEZAWA,
Analytical Sciences. 19, 499–504 (2003).
DOI:10.2116/analsci.19.499
A genetic approach to identifying mitochondrial proteins. T. Ozawa, Y. Sako, M. Sato, T. Kitamura, Y. Umezawa,
Nature Biotechnology. 21, 287–293 (2003).
DOI:10.1038/nbt791
Y. Umezawa, T. Ozawa, M. Sato, Probing Chemical Processes in Living Cells: Applications for Assay and Screening of Chemicals that Disrupt Cellular Signaling Pathways. Bulletin of the Chemical Society of Japan. 75, 1423–1433 (2002).
DOI:10.1246/bcsj.75.1423
Fluorescent indicators for imaging protein phosphorylation in single living cells.
M. Sato, T. Ozawa, K. Inukai, T. Asano, Y. Umezawa,
Nature Biotechnology. 20, 287–294 (2002).
DOI:10.1038/nbt0302-287
Peptide Assemblies in Living Cells. Methods for Detecting Protein-Protein Interactions†.
T. Ozawa, Y. Umezawa,
Supramolecular Chemistry. 14, 271–280 (2002).
DOI:10.1080/10610270290026185
Protein Splicing-Based Reconstitution of Split Green Fluorescent Protein for Monitoring Protein−Protein Interactions in Bacteria: Improved Sensitivity and Reduced Screening Time.
T. Ozawa, M. Takeuchi, A. Kaihara, M. Sato, Y. Umezawa,
Analytical Chemistry. 73, 5866–5874 (2001).
DOI:10.1021/ac010717k
Screening method for antagonists that inhibit the binding of calmodulin to a target peptide using surface plasmon resonance.
K. Sasaki, T. Ozawa, Y. Umezawa,
Analytica Chimica Acta. 447, 63–74 (2001).
DOI:10.1016/S0003-2670(01)01290-9
Detection of Protein-Protein Interactions in vivo Based on Protein Splicing.
T. Ozawa and Y. Umezawa,
Current Opinion in Chemical Biology, 5, 578-583 (2001).
DOI:10.1016/S1367-5931(00)00244-1
Imaging of Conformational Changes of Proteins with a New Environment-Sensitive Fluorescent Probe Designed for Site-Specific Labeling of Recombinant Proteins in Live Cells.
J. Nakanishi, T. Nakajima, M, Sato, T, Ozawa, K. Tohda and Y. Umezawa,
Analytical Chemistry, 73, 2920-2928 (2001).
DOI:10.1021/ac001528pPubMed:11467536
Split Luciferase as an Optical Probe for Detecting Protein—Protein Interactions in Mammalian Cells Based on Protein Splicing.
T. Ozawa, A. Kaihara, M. Sato, K. Tachihara and Y. Umezawa,
Analytical Chemistry, 73, 2516-2521 (2001).
DOI:10.1021/ac0013296
Fluorescent Indicators for Cyclic GMP Based on Cyclic GMP-Dependent Protein Kinase Ia and Green Fluorescent Proteins.
M. Sato, N. Hida, T. Ozawa and Y. Umezawa,
Analytical Chemistry, 72, 5918-5924 (2000).
DOI:10.1021/ac0006167
A Screening Method for Substrates of Multidrug Resistance-associated Protein (MRP).
Z. Quan, T. Ozawa, M. Sato and Y. Umezawa,
Analytical Chim. Acta, 423, 197-203 (2000).
DOI:10.1016/S0003-2670(00)01116-8
How Can Ca²⁺ Selectively Activate Recoverin in the Presence of Mg²⁺? Surface Plasmon Resonance and FT-IR Spectroscopic Studies.
T. Ozawa, M. Fukuda, M. Nara, A. Nakamura, K. Kohama and Y. Umezawa,
Biochemistry, 39, 14495-14503 (2000).
DOI:10.1021/bi001930y
A Fluorescent Indicator for Detecting Protein–Protein Interactions in Vivo Based on Protein Splicing.
T. Ozawa, S. Nogami, M. Sato, Y. Ohya and Y. Umezawa,
Analytical Chemistry, 72, No. 21, 5151-5157 (2000).
DOI:10.1021/ac000617z
Novel Interaction of the Voltage-Dependent Sodium Channel (VDSC) with Calmodulin: Does VDSC Acquire Calmodulin-Mediated Ca²⁺-Sensitivity?
M. Mori, T. Konno, T. Ozawa, M. Murata, K. Imoto and K. Nagayama,
Biochemistry, 39, 1316-1323 (2000).
DOI:10.1021/bi9912600
An SPR-based Screening Method for Agonist Selectivity for Insulin Signaling Pathways Based on the Binding of Phosphotyrosine to its Specific Binding Protein.
T. Yoshida, M. Sato, T. Ozawa and Y. Umezawa,
DOI:10.1021/ac990795w
Metal Ion Selectivity for Formation of the Calmodulin-Metal-Target Peptide Ternary Complex Studied by Surface Plasmon Resonance Spectroscopy.
T. Ozawa, K. Sasaki and Y. Umezawa,
Biochimica et Biophysica Acta, 1434, 211-220 (1999).
DOI:10.1016/S0167-4838(99)00185-5
A Fluorescent Indicator for Tyrosine Phosphorylation-Based Insulin Signaling Pathways.
M. Sato, T. Ozawa, T. Yoshida and Y. Umezawa,
Analytical Chemistry, 71, 3948-3954 (1999)
DOI:10.1021/ac990318d
An Assay Method for Evaluating Chemical Selectivity of Agonists for Insulin Signaling Pathways Based on Agonist-Induced Phosphorylation of a Target Peptide.
T. Ozawa, M. Sato, M. Sugawara and Y. Umezawa,
Analytical Chemistry, 70, 2345-2352 (1998).
DOI:10.1021/ac971192s
An Optical Method for Evaluating Ion Selectivity for Calcium Signaling Pathways in the Cell.
T. Ozawa, M. Kakuta, M. Sugawara, Y. Umezawa and M. Ikura,
Analytical Chemistry, 69, 3081-3085 (1997).
DOI:10.1021/ac9613141

Reviews

2022

Dumancas, G.G., Subong, B.J.J. Ozawa, T. Rodney, T.L. Hikkaduwa Koralege, R.S., Pham-Bugayong, P.J. Thiabendazole. Encyclopedia of Toxicology, 4^th edition (Elsevier)（2022）．
「先端の分析法（第２版）」澤田嗣郎監修，小澤岳昌，北森武彦，中村洋，藤浪眞紀，宮村一夫編集，NTS(2022).
「FRETプローブ：先端の分析法（第２版）」上田善文，小澤岳昌，NTS，p324-328(2022).
「タンパク質再構成法：先端の分析法（第２版）」小澤岳昌，NTS，p329-332(2022).
「蛍光共鳴エネルギー移動（FRET）顕微鏡：先端の分析法（第２版）」上田善文，小澤岳昌，NTS，p374-375(2022).

2021

M Endo, T Ozawa, Functional Modulation of Receptor Proteins on Cellular Interface with Optogenetic System. Optogenetics, 2274, 247–263 (2021).
Takamura, Ayari, Ozawa, Takeaki. Recent advances of vibrational spectroscopy and chemometrics for forensic biological analysis. Analyst 146, 7431–7449 (2021).
DOI:10.1007/978-1-0716-1258-3_7
尾崎倫孝，小澤岳昌,. 生体分子機能を可視化する発光イメージングと応用技術 OPTRONICS 40, 104–110 (2021).
Littmann, Timo, Ozawa, Takeaki, Bernhardt, Günther. Quantitative Determination and Imaging of Gαq Signaling in Live Cells via Split-Luciferase Complementation. Methods. Mol. Biol. 2274, 69–78 (2021).
DOI:10.1007/978-1-0716-1258-3_7
Li, Qiaojing, Yoshimura, Hideaki, Ozawa, Takeaki. A Split-Luciferase-Based Cell Fusion Assay for Evaluating the Myogenesis-Promoting Effects of Bioactive Molecules. Methods. Mol. Biol. 2274, 79–87 (2021).
DOI:10.1007/978-1-0716-1258-3_8
Takenouchi, Osamu, Yoshimura, Hideaki, Ozawa, Takeaki. Quantitative Analysis of Membrane Receptor Trafficking Manipulated by Optogenetic Tools. Methods. Mol. Biol. 2274, 15–23 (2021)..
DOI:10.1007/978-1-0716-1258-3_2
Endo, Mizuki, Ozawa, Takeaki. Functional Modulation of Receptor Proteins on Cellular Interface with Optogenetic System. Adv. Exp. Med. Biol. 1293, 247-263 (2021).
DOI:10.1007/978-981-15-8763-4_15
Endo, Mizuki, Ozawa, Takeaki. Advanced Bioluminescence System for In Vivo Imaging with Brighter and Red-Shifted Light Emission. Int. J. Mol. Sci. 21, 6538 (2021).
DOI:10.3390/ijms21186538

2020

小澤岳昌. バイオイメージング. 東京, 共立出版, 2020, ISBN978-4-320-04457-9.
Yamada, Mayumi, Nagasaki, Shinji C., Ozawa, Takeaki, Imayoshi, Itaru. Light-mediated control of Gene expression in mammalian cells. Neuroscience Research. 2020, vol. 152, p. 66–77. https://linkinghub.elsevier.com/retrieve/pii/S0168010219306807.
DOI:10.1016/j.neures.2019.12.018

2019

吉村英哲, 小澤岳昌. “二分割ルシフェラーゼ再構成法による発光プローブ”. 発光イメージング実験ガイド. 永井健治, 小澤岳昌編. 羊土社, 2019, p. 62–70.
小澤岳昌 (訳). スクーグ分析化学, West Skoog and Holler Crouch (著). 東京化学同人, 2019.
小澤岳昌. “アポトーシスの発光イメージング”. 発光イメージング実験ガイド. 永井健治, 小澤岳昌編. 羊土社, 2019, p. 91–95.
Yoshimura, Hideaki, Ozawa, Takeaki. “Optical Control of G Protein-Coupled Receptor Activities in Living Cells”. Springer Series in Chemical Physics. 2019, p. 129–138. http://link.springer.com/10.1007/978-3-030-05974-3_7.
DOI:10.1007/978-3-030-05974-3_7

2018

Vriz, Sophie, Ozawa, Takeaki. Optogenetics. Cambridge, Royal Society of Chemistry, 2018, (Comprehensive Series in Photochemical &Photobiological Sciences), ISBN978-1-78801-237-9. http://dx.doi.org/10.1039/9781788013284 http://ebook.rsc.org/?DOI=10.1039/9781788013284.
DOI:10.1039/9781788013284
Kawamura, Genki, Ozawa, Takeaki. “CHAPTER 8. Quantitative Control of Kinase Activity with a Mathematical Model”. Optogenetics: Light-driven Actuators and Light-emitting Sensors in Cell Biology. Vriz, Sophie, Ozawa, Takeaki編. 2018, p. 149–168, ISBN978-1-78801-237-9. http://ebook.rsc.org/?DOI=10.1039/9781788013284-00149.
DOI:10.1039/9781788013284-00149
小澤岳昌. “第3章プローブタンパク質”. 蛍光イメージング/MRIプローブの開発. シーエムシー出版, 2018, p. 22–34.
吉村英哲, 小澤岳昌. “生命分子の機能を超えるための解析化学”. 生命機能に迫る分子化学. 化学同人, 2018, p. 28–33.
Yoshimura, Hideaki, Ozawa, Takeaki. “Real-Time Fluorescence Imaging of Single-Molecule Endogenous Noncoding RNA in Living Cells”. Methods in Molecular Biology. 2018, p. 337–347. http://link.springer.com/10.1007/978-1-4939-7213-5_22.
DOI:10.1007/978-1-4939-7213-5_22
OZAWA, Takeaki. Nano-Materials for Bioimaging. Analytical Sciences. 2018, vol. 34, no. 2, p. 125–126. https://www.jstage.jst.go.jp/article/analsci/34/2/34_125/_article.
DOI:10.2116/analsci.34.125

2017

小澤岳昌. 日本分析化学会英文誌の情報発信強化策. 情報管理. 2017, vol. 60, no. 1, p. 37–42.
DOI:10.1241/johokanri.60.37
小澤岳昌. “クリスチャン Excelで解く分析化学 3化学平衡の一般概念”. Analytical Chemistry 7th edition 訳. 丸善出版, 2017, p. 29–38.
遠藤瑞己, 小澤岳昌. 光誘導性二量体・多量体形成システムを用いた受容体タンパク質活性の制御. 生体の科学. 2017, vol. 68, p. 494–495.
Ozawa, Takeaki. “Luminescent Sensors for Single-Cell Analysis”. Springer Series in Chemical Physics. 2017, p. 97–107. http://link.springer.com/10.1007/978-3-319-52431-3_9.
DOI:10.1007/978-3-319-52431-3_9
Endo, M., Ozawa, T. Strategies for development of optogenetic systems and their applications. Journal of Photochemistry and Photobiology C: Photochemistry Reviews. 2017, vol. 30, no. SI, p. 10–23. https://linkinghub.elsevier.com/retrieve/pii/S1389556716300612.
DOI:10.1016/j.jphotochemrev.2016.10.003

2016

小澤岳昌. “クリスチャン分析化学 I. 基礎編. 6章化学平衡の一般概念”. Analytical Chemistry 7th edition 訳. 丸善出版, 2016, p. 179–206.
服部満, 小澤岳昌. “三次元発光イメージング”. 先端計測・研究を支える機器開発. 化学同人, 2016, p. 82–87.
Kim, Sung Bae, Ozawa, Takeaki, Umezawa, Yoshio. A genetically encoded bioluminescent indicator for illuminating proinflammatory cytokines. MethodsX. 2016, vol. 3, p. 483–489. https://linkinghub.elsevier.com/retrieve/pii/S2215016116300255.
DOI:10.1016/j.mex.2016.06.001
Yoshimura, H., Ozawa, T. “Monitoring of RNA Dynamics in Living Cells Using PUM-HD and Fluorescent Protein Reconstitution Technique”. VISUALIZING RNA DYNAMICS IN THE CELL. Filonov, G. S., Jaffrey, S. R.編. 525 B STREET, SUITE 1900, SAN DIEGO, CA 92101-4495 USA, ELSEVIER ACADEMIC PRESS INC, 2016, p. 65–85, (Methods in Enzymology), ISBN978-0-12-802488-1 978-0-12-802292-4. https://linkinghub.elsevier.com/retrieve/pii/S0076687916001300.
DOI:10.1016/bs.mie.2016.03.018
Hattori, Mitsuru, Ozawa, Takeaki. “Live Cell Bioluminescence Imaging in Temporal Reaction of G Protein-Coupled Receptor for High-Throughput Screening and Analysis”. Methods in Molecular Biology. 2016, p. 195–202. http://link.springer.com/10.1007/978-1-4939-3813-1_16.
DOI:10.1007/978-1-4939-3813-1_16

2015

菅野憲, 小澤岳昌. “発光の生物 -6.1.2 液相化学発光反応”. 発光の事典. 朝倉書店, 2015, p. 488–493.
小澤岳昌. ジャーナル戦国時代. ぶんせき. 2015, vol. 9, p. 371.
菅野憲, 小澤岳昌. “発光の生物 -6.1.1 化学発光概説”. 発光の事典. 朝倉書店, 2015, p. 482–488.
菅野憲, 小澤岳昌. “発光の生物 -7.2 2.2再構成法”. 発光の事典. 朝倉書店, 2015, p. 616–623.
菅野憲, 小澤岳昌. “発光の生物 -7.1.6 化学発光”. 発光の事典. 朝倉書店, 2015, p. 561–570.
Hattori, Mitsuru, Ozawa, Takeaki. Bioluminescent tools for the analysis of G-protein-coupled receptor and arrestin interactions. RSC Advances. 2015, vol. 5, no. 17, p. 12655–12663. http://xlink.rsc.org/?DOI=C4RA14979C.
DOI:10.1039/C4RA14979C
Takakura, Hideo, Hattori, Mitsuru, Tanaka, Miho, Ozawa, Takeaki. “Cell-Based Assays and Animal Models for GPCR Drug Screening”. Methods in Molecular Biology. Prazeres, D. M. F., Martins, S. A. M.編. 999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA, HUMANA PRESS INC, 2015, p. 257–270, (Methods in Molecular Biology), ISBN978-1-4939-2336-6. http://link.springer.com/10.1007/978-1-4939-2336-6_18.
DOI:10.1007/978-1-4939-2336-6_18
Ozawa, Takeaki. “Molecular Imaging for Bioanalysis” Analytical Sciences. 2015, vol. 31, no. 4, p. 243–243. https://www.jstage.jst.go.jp/article/analsci/31/4/31_243/_article.
DOI:10.2116/analsci.31.243
吉村英哲, 小澤岳昌. 蛍光顕微鏡を用いた生細胞内1分子可視化解析法. ナノ学会会報. 2015, vol. 13, no. 2, p. 61–65.
吉村英哲, 小澤岳昌. 生細胞内RNAイメージング. 細胞工学. 2015, vol. 34, p. 53–58.

2014

服部満, 田中みほ, 小澤岳昌. “GPCRに作用する化合物のスクリーニング”. Clinical Neuroscience. 中外医学社, 2014, p. 128–129.
HATTORI, Mitsuru, OZAWA, Takeaki. Split Luciferase Complementation for Analysis of Intracellular Signaling. Analytical Sciences. 2014, vol. 30, no. 5, p. 539–544. http://jlc.jst.go.jp/DN/JST.JSTAGE/analsci/30.539?lang=en&from=CrossRef&type=abstract.
DOI:10.2116/analsci.30.539
Yoshimura, Hideaki, Ozawa, Takeaki. Methods of Split Reporter Reconstitution for the Analysis of Biomolecules. The Chemical Record. 2014, vol. 14, no. 3, p. 492–501. http://doi.wiley.com/10.1002/tcr.201402001.
DOI:10.1002/tcr.201402001

2013

Kim, Sung, Ozawa, Takeaki. Fabrication of Split-Luciferase Complementation Assays for Molecular Imaging. Current Molecular Imaging. 2013, vol. 2, no. 2, p. 148–157. http://www.eurekaselect.com/openurl/content.php?genre=article&issn=2211-5552&volume=2&issue=2&spage=148.
DOI:10.2174/22115552113029990001
Ozawa, Takeaki, Yoshimura, Hideaki, Kim, Sung Bae. Advances in Fluorescence and Bioluminescence Imaging. Analytical Chemistry. 2013, vol. 85, no. 2, p. 590–609. https://pubs.acs.org/doi/10.1021/ac3031724.
DOI:10.1021/ac3031724
金誠培, 小澤岳昌, 長縄竜一. ホルモン診断に資するルミネセンス分析技術の進歩. ぶんせき. 2013, vol. 467, p. 678–686.

2012

宮脇敦史, 小澤岳昌, 高松哲郎, 長野哲雄. 分子イメージング−基礎から創薬までの新展開（座談会）. ヒューマンサイエンス. 2012, vol. 23, no. 4, p. 4–11.
服部満, 小澤岳昌. “タンパク質翻訳後修飾細胞内イメージング”. ここまで進んだバイオセンシング・イメージング. 日本化学会編. 化学同人, 2012, p. 108–113.
小澤岳昌. 生体分子と細胞内シグナルの可視化分析法. ヒューマンサイエンス. 2012, vol. 23, no. 4, p. 12–16.
Kim, Sung, Hattori, Mitsuru, Ozawa, Takeaki. Intelligent Design of Nano-Scale Molecular Imaging Agents. International Journal of Molecular Sciences. 2012, vol. 13, no. 12, p. 16986–17005. http://www.mdpi.com/1422-0067/13/12/16986.
DOI:10.3390/ijms131216986

2011

菅野憲, 小澤岳昌. “対象別試料分析法 5.4.5 細胞”. 分析化学便覧. 日本分析化学会編編. 化学同人, 2011, p. 516–522.
佐藤健太郎, 小澤岳昌. 写真で見る日本化学の源流. 化学. 2011, vol. 66, p. 43–47.
上村想太郎, 小澤岳昌, 加地範国, 権田幸祐. 見つけることに意義がある—1分子計測技術の可能性—. 現代化学. 2011, vol. 488, p. 26–30.
小澤岳昌. “プローブタンパク質”. 蛍光イメージング/MRIプローブの開発. 菊地和也監修編. シーエムシー出版, 2011, p. 22–34.
岳昌小澤. 生命分子科学. 学術の動向. 2011, vol. 16, no. 5, p. 5_53-5_57.
DOI:10.5363/tits.16.5_53
Awais, Muhammad, Ozawa, Takeaki. Illuminating intracellular signaling and molecules for single cell analysis. Molecular BioSystems. 2011, vol. 7, no. 5, p. 1376. http://xlink.rsc.org/?DOI=c0mb00328j.
DOI:10.1039/c0mb00328j
Kanno, Akira, Ozawa, Takeaki, Umezawa, Yoshio. “Detection of Protein–Protein Interactions in Bacteria by GFP-Fragment Reconstitution”. HETEROLOGOUS GENE EXPRESSION IN E COLI: METHODS AND PROTOCOLS. Evans, T. C., Xu, Q. M 編. 999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA, HUMANA PRESS INC, 2011, p. 251–258, (Methods in Molecular Biology), ISBN978-1-61737-966-6. http://link.springer.com/10.1007/978-1-61737-967-3_15.
DOI:10.1007/978-1-61737-967-3_15
菅野憲, 小澤岳昌. タンパク質核内移行の可視化. 生体の科学. 2011, vol. 65, p. 494–495.
Ozawa, Takeaki, Umezawa, Yoshio. Imaging of Endogenous RNA Using Genetically Encoded Probes. Current Protocols in Chemical Biology. 2011, vol. 3, no. 1, p. 27–37. https://onlinelibrary.wiley.com/doi/abs/10.1002/9780470559277.ch100152.
DOI:10.1002/9780470559277.ch100152
小澤岳昌. 発光タンパク質による細胞活動リアルタイム観察. Bioindustry. 2011, vol. 28, p. 11–17.
Ozawa, Takeaki, Umezawa, Yoshio. “Genetically-Encoded Fluorescent Probes for Imaging Endogenous mRNA in Living Cells”. RNA DETECTION AND VISUALIZATION: METHODS AND PROTOCOLS. Gerst JE編. 999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA, HUMANA PRESS INC, 2011, p. 175–188, (Methods in Molecular Biology), ISBN978-1-61779-004-1. http://link.springer.com/10.1007/978-1-61779-005-8_11.
DOI:10.1007/978-1-61779-005-8_11

2010 and before

小澤岳昌. “生体分子と生理機能を可視化するタンパク質再構成法”. シングルセル解析の最前線. 神原秀記, 松永是, 植田充美（監修）編. シーエムシー出版, 2010, p. 40–48.
小澤岳昌. “生細胞内ｍRNAイメージングの現状と課題”. 生命現象を理解する分子ツール. 浜地格, 二木史朗編. 化学同人, 2010, p. 33–40, (化学フロンティア（２２）).
小澤岳昌. 蛍光・発光タンパク質を用いた再構成法による分子イメージング. 実験医学. 2010, vol. 28, p. 27–32.
小澤岳昌. 発光タンパク質で細胞内をみる. 未来材料. 2009, vol. 9, p. 28–35.
小澤岳昌. “RNAとタンパク質局在のイメージング（新しい地平をひらく分析手法の最前線）”. 化学フロンティア. 北森武彦編. 化学同人, 2009, p. 111–118.
小澤岳昌. “蛍光タンパク質の設計と応用”. 超分子・サイエンス＆テクノロジー. 国武豊喜編. エヌ・ティー・エス, 2009, p. 880–889.
小澤岳昌. 新領域開拓の先導的立場を担う化学. 化学. 2009, vol. 64, p. 21–22.
小澤岳昌 (監訳), 大森充香（訳）. 光る遺伝子, Mark Zimmer (著). 丸善, 2009.
小澤岳昌. 生体分子の機能を可視化するＧＦＰ再構成法. 化学と工業. 2009, vol. 62, p. 129–132.
Kanno, Akira, Umezawa, Yoshio, Ozawa, Takeaki. “Detection of Apoptosis Using Cyclic Luciferase in Living Mammals”. BIOLUMINESCENCE: METHODS AND PROTOCOLS, SECOND EDITION. Rich, P. B., Douillet, C.編. 999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA, HUMANA PRESS INC, 2009, p. 105–114, (Methods in Molecular Biology), ISBN978-1-60327-320-6. http://link.springer.com/10.1007/978-1-60327-321-3_9.
DOI:10.1007/978-1-60327-321-3_9
Kanno, Akira, Ozawa, Takeaki, Umezawa, Yoshio. “Bioluminescent Imaging of MAPK Function with Intein-Mediated Reporter Gene Assay”. BIOLUMINESCENCE: METHODS AND PROTOCOLS, SECOND EDITION. Rich, P. B., Douillet, C.編. 999 RIVERVIEW DR, STE 208, TOTOWA, NJ 07512-1165 USA, HUMANA PRESS INC, 2009, p. 185–192, (Methods in Molecular Biology), ISBN978-1-60327-320-6. http://link.springer.com/10.1007/978-1-60327-321-3_15.
DOI:10.1007/978-1-60327-321-3_15
OZAWA, Takeaki. Protein Reconstitution Methods for Visualizing Biomolecular Function in Living Cells. YAKUGAKU ZASSHI. 2009, vol. 129, no. 3, p. 289–295. https://www.jstage.jst.go.jp/article/yakushi/129/3/129_3_289/_article.
DOI:10.1248/yakushi.129.289
小澤岳昌, 宮脇敦史. クラゲから生まれたGFP革命. 現代化学. 2008, no. 12, p. 25–28.
小澤岳昌. “可視化プローブによる時空間情報を損なわないミトコンドリアRNAの動態観察”. ナノイメージング. エヌ・ティー・エス, 2008, p. 199–206.
小澤岳昌. “生理機能を可視化する新たな分子プローブ”. ナノメディシン. 宇理須恒雄編. オーム社, 2008, p. 13–24.
Ozawa, Takeaki. Molecular Science for Analyzing Dynamics of Biomolecules in Living Cells. Journal of Japan Society of Computer Aided Surgery. 2008, vol. 10, no. 4, p. 489–493. https://www.jstage.jst.go.jp/article/jscas1999/10/4/10_4_489/_article.
DOI:10.5759/jscas1999.10.489
小澤岳昌. RNAイメージング法. 実験医学増刊. 2008, vol. 26, p. 59–67.
小澤岳昌. タンパク質再構成法を用いた細胞内生体分子の解析法. BIOINDUSTRY. 2008, vol. 25, p. 27–36.
菅野憲, 小澤岳昌. レポータータンパク質の再構成法を利用した生体分子イメージング. 生体の科学. 2008, vol. 59, p. 66–72.
小澤岳昌. “細胞の構造と機能：細胞内”. ナノテクのためのバイオ入門. 荻野俊郎, 宇理須恒雄編. 共立出版, 2007.
Ozawa, Takeaki, Umezawa, Yoshio. A Genetic Method to Identify Mitochondrial Proteins in Living Mammalian Cells. Protein Targeting Protocols. 2007, p. 119–130. http://link.springer.com/10.1007/978-1-59745-466-7_8.
DOI:10.1007/978-1-59745-466-7_8PubMed:17951684
Ozawa, Takeaki, Umezawa, Yoshio. Identification of Proteins Targeted Into the Endoplasmic Reticulum by cDNA Library Screening. Protein Targeting Protocols. 2007, p. 269–280. http://link.springer.com/10.1007/978-1-59745-466-7_18.
DOI:10.1007/978-1-59745-466-7_18
Wei, Chiming, Yamato, Masayuki, Wei, Wenchi, Zhao, Xiaojun, Tsumoto, Kanta, Yoshimura, Tetsuro, Ozawa, Takeaki, Chen, Yu-Ju. Genetic Nanomedicine and Tissue Engineering. Medical Clinics of North America. 2007, vol. 91, no. 5, p. 889–898. https://linkinghub.elsevier.com/retrieve/pii/S0025712507000636.
DOI:10.1016/j.mcna.2007.05.001
小澤岳昌. 光プローブの新しいデザインと生体機能の可視化. 化学工業. 2007, vol. 58, p. 860–864.
小澤岳昌. “バイオテクノロジーにおける生物発光”. バイオ・ケミルミネセンスハンドブック. 今井一洋, 近江谷克裕編. 丸善株式会社, 2006.
Takeuchi, Masaki, Ozawa, Takeaki. Frontiers in Bioimaging. ACS Chemical Biology. 2006, vol. 1, no. 6, p. 333–334. https://pubs.acs.org/doi/10.1021/cb600266h.
DOI:10.1021/cb600266h
小澤岳昌, 梅澤喜夫. 新しい蛍光タンパク質とその応用. ゲノム医学. 2006, vol. 6, p. 277–280.
小澤岳昌. フローサイトメーター. ぶんせき. 2006, vol. 384, p. 640–641.
小澤岳昌. タンパク質の局在を知るープロテインスプライシングを利用したイメージング技術の開発. バイオニクス. 2006, vol. 3, p. 52–57.
小澤岳昌. スプリットルシフェラーゼを用いた細胞内シグナル解析法. バイオテクノロジージャーナル. 2006, vol. 6, p. 225–228.
OZAWA, Takeaki. Proteins for Visualizing Intracellular Signaling (細胞内情報を視覚化するタンパク質試薬). Kobunshi. 2006, vol. 55, no. 5, p. 343–343. http://joi.jlc.jst.go.jp/JST.Journalarchive/kobunshi1952/55.343?from=CrossRef.
DOI:10.1295/kobunshi.55.343
小澤岳昌. マウス個体におけるタンパク質動態イメージング. 細胞工学. 2006, vol. 25, p. 1019–1022.
小澤岳昌. “ミトコンドリア局在タンパク質を同定するプローブ分子”. 化学測定の辞典. 梅澤喜夫編. 朝倉書店, 2005.
“Inteins for Split-Protein Reconstitutions and Their Applications”. Nucleic Acids and Molecular Biology, Vol. 16. Ozawa, T., Umezawa, Y., Belfort, M.編. Springer-Verlag/Berlin, 2005, p. 307–323.
Umezawa, Y., Ozawa, T., Sato, M., Inadera, H., Kaneko, S., Kunimoto, M., Hashimoto, S. Methods of analysis for chemicals that disrupt cellular signaling pathways: risk assessment for potential endocrine disruptors. Enviromental Sciences. 2005, vol. 12, p. 49–64.
PubMed:15793560
小澤岳昌. “Reporter gene assay”. 先端の分析法—理工学からナノ・バイオまで. 梅澤喜夫, 澤田嗣郎, 寺部茂編. エヌ・ティー・エス, 2004.
小澤岳昌. “細胞内オルガネラ局在タンパク質同定法”. 先端の分析法—理工学からナノ・バイオまで. 梅澤喜夫, 澤田嗣郎, 寺部茂編. エヌ・ティー・エス, 2004.
小澤岳昌. “Western blotting”. 先端の分析法—理工学からナノ・バイオまで. 梅澤喜夫, 澤田嗣郎, 寺部茂編. エヌ・ティー・エス, 2004.
小澤岳昌. 高等動物にも存在したプロテインスプライシング. 化学. 2004, no. 9, p. 61–62.
小澤岳昌. “FACS”. 先端の分析法—理工学からナノ・バイオまで. 梅澤喜夫, 澤田嗣郎, 寺部茂編. エヌ・ティー・エス, 2004.
小澤岳昌. “カット＆ペースト”で機能性タンパク質をつくるープロテインスプライシングに学ぶ合成技術—. 現代科学. 2004, no. 5, p. 49–54.
小澤岳昌. “酵母two-hybrid法（in vivo）ほか”. 先端の分析法—理工学からナノ・バイオまで. 梅澤喜夫, 澤田嗣郎, 寺部茂編. エヌ・ティー・エス, 2004.
小澤岳昌. 蛍光・発光タンパク質プローブの新たなデザインと細胞内オルガネラを標的としたプロテオミクス. ぶんせき. 2004, vol. 359, p. 637–639.
小澤岳昌, 梅澤喜夫. タンパク質間相互作用の生体での非破壊イメージング. 実験医学. 2004, vol. 22, p. 529–533.
佐藤守俊，小澤岳昌，梅澤喜夫. タンパク質プローブ. 現代科学. 2003, no. 2, p. 25–31.
梅澤喜夫, 佐藤守俊, 小澤岳昌. 生細胞内情報伝達の蛍光可視化プローブ. ぶんせき. 2003, vol. 337, p. 18–25.
小澤岳昌. 環境—環境汚染物質のリスク評価・高速スクリーニング法—. ぶんせき. 2003, vol. 346, p. 592–596.
小澤岳昌. インテイン. Molecular Medicine. 2003, vol. 40, p. 1384–1386.
Ozawa, Takeaki, Sako, Yusuke, Sato, Moritoshi, Kitamura, Toshio, Umezawa, Yoshio. A genetic approach to identifying organelle-localized proteins. Proc. ISBC 2003. 2003, p. 276–279.
小澤岳昌. “表面プラズモン共鳴法”. 機器分析実験. 梅澤喜夫, 本水昌二, 渡会仁, 寺前紀夫編. 東京化学同人, 2002.
小澤岳昌. “共焦点レーザー走査型蛍光顕微鏡”. 機器分析実験. 梅澤喜夫, 本水昌二, 渡会仁, 寺前紀夫編. 東京化学同人, 2002.
Umezawa, Yoshio, Ozawa, Takeaki, Sato, Moritoshi. Methods of Analysis for Chemicals that Promote/Disrupt Cellular Signaling. Analytical Sciences. 2002, vol. 18, no. 5, p. 503–516. http://joi.jlc.jst.go.jp/JST.JSTAGE/analsci/18.503?from=CrossRef.
DOI:10.2116/analsci.18.503
Umezawa, Yoshio, Ozawa, Takeaki, Sato, Moritoshi. Probing Chemical Processes in Living Cells: Applications for Assay and Screening of Chemicals that Disrupt Cellular Signaling Pathways. Bulletin of the Chemical Society of Japan. 2002, vol. 75, no. 7, p. 1423–1433. http://www.journal.csj.jp/doi/10.1246/bcsj.75.1423.
DOI:10.1246/bcsj.75.1423
Umezawa, Y., Ozawa, T., Sato, M. Assay and Screening Methods for Chemicals that Disrupt Cellular Signaling Pathways. Risk Assessment for Potential Endocrine Disruptors. Environmental Sciences. 2002, vol. 9, p. 23–35.
Ozawa, Takeaki, Umezawa, Yoshio. Peptide Assemblies in Living Cells. Methods for Detecting Protein-Protein Interactions†. Supramolecular Chemistry. 2002, vol. 14, no. 2–3, p. 271–280. https://www.tandfonline.com/doi/full/10.1080/10610270290026185.
DOI:10.1080/10610270290026185
小澤岳昌. “共焦点レーザ走査型蛍光顕微鏡”. 界面ハンドブック. 岩澤康裕, 梅澤喜夫, 澤田嗣郎, 辻井薫編. エヌ・ティー・エス, 2001.
小澤岳昌. “固定化ペプチド”. 界面ハンドブック. 岩澤康裕, 梅澤喜夫, 澤田嗣郎, 辻井薫編. エヌ・ティー・エス, 2001.
Ozawa, Takeaki, Umezawa, Yoshio. Detection of protein–protein interactions in vivo based on protein splicing. Current Opinion in Chemical Biology. 2001, vol. 5, no. 5, p. 578–583. https://linkinghub.elsevier.com/retrieve/pii/S1367593100002441.
DOI:10.1016/S1367-5931(00)00244-1
小澤岳昌, 梅澤喜夫. 内分泌撹乱化学物質の細胞内標的分子の同定と新しいバイオモニタリング．（特集：内分泌撹乱化学物質（環境ホルモン）とその問題点）. 産婦人科の実際. 2000, vol. 49, p. 1113–1122.
小澤岳昌, 梅澤喜夫. “膜レセプタセンサ”. 最新の分離・精製・検出法〜原理から応用まで. 梅澤喜夫, 澤田嗣郎, 中村洋編. エヌ・ティー・エス, 1997.
平野愛弓, 小澤岳昌, 菅原正雄, 梅澤喜夫（分担執筆）. “信号伝達のバイオセンサー”. 生物のスーパーセンサー. 生物物理学会編. 共立出版, 1997, p. 172–181.
Sugawara, M., Sato, H., Ozawa, T., Umezawa. “Receptor Based Chemical Sensing”. Frontiers in Biosensorics, I, Fundamental Aspects. Y., Sheller, F. W., Schubert, F., Fedrowitz, J.編. Birkhäuser Verlag Basel/Switzerland, 1997, p. 121–131.
菅原正雄, 小澤岳昌, 平野愛弓, 中西淳, 佐藤守俊, 梅澤喜夫. レセプター蛋白に基づく化学センシング −生理適合性を有するアゴニスト選択性の評価法−. 表面. 1997, vol. 35, p. 660–668.