Jun Ohata

A histochemical approach to activity- based copper sensing reveals cuproplasia- dependent vulnerabilities in cancer

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 122(3).

Catalytic Serine Labeling in Nonaqueous, Acidic Media

Ishizawa, S., Uzoewulu, C. P., Iwakura, Y., Koirala, A., Sato, S., & Ohata, J. (2025, February 9). CHEMISTRY-A EUROPEAN JOURNAL, Vol. 2.

InP-Based Quantum Dots as Photosensitizers in Photodynamic Antimicrobial Materials

Chen, L., Jiang, C., Scholle, F., Meo, A. E., Ohata, J., Gorman, C. B., & Ghiladi, R. A. (2025, January 16). ACS APPLIED BIO MATERIALS, Vol. 1.

Catalysis in Protein Bioconjugation

Ishizawa, S., Fujimura, K., Oisaki, K., Sato, S., & Ohata, J. (2024, December 27).

Catalytic Serine Labeling in Nonaqueous, Acidic Media

Ishizawa, S., Uzoewulu, C., Iwakura, Y., Koirala, A., Sato, S., & Ohata, J. (2024, September 27).

Contextual Analysis of Scientific Publications for Advancing Writing Skills (CASPArS): Self-Learning for Science Writing Using Top Scientists' Literature

Ohata, J., Martin, J. D., & Ison, A. (2024, December 6). JOURNAL OF CHEMICAL EDUCATION, Vol. 12.

Contextual Analysis of Scientific Publications for Advancing writing Skills (CASPArS): Self-Learning for Science Writing Using Top Scientists’ Literature

Ohata, J., Martin, J. D., & Ison, A. (2024, May 28).

Fluoroalcohols for chemical modification of biomolecules

Tetrahedron Chem.

Friedel-Crafts Reactions for Biomolecular Chemistry

Ohata, J. (2024, March 12).

Friedel-Crafts reactions for biomolecular chemistry

Ohata, J. (2024, April 9). ORGANIC & BIOMOLECULAR CHEMISTRY, Vol. 4.

Hexafluoroisopropanol as a Bioconjugation Medium of Ultrafast, Tryptophan-Selective Catalysis

Nuruzzaman, M., Colella, B. M., Uzoewulu, C. P., Meo, A. E., Gross, E. J., Ishizawa, S., … Ohata, J. (2024, February 29). JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, Vol. 2.

Redox-neutral, metal-free tryptophan labeling of polypeptides in hexafluoroisopropanol (HFIP)

Nuruzzaman, M., Colella, B. M., Nizam, Z. M., Cho, I. J. H., Zagorski, J., & Ohata, J. (2024, August 26). RSC CHEMICAL BIOLOGY, Vol. 8.

Chemical labeling strategies using biomolecule-compatible, nonaqueous media

Ohata, J. (2023, September 27). [Data Management Plan]. DMPTool.].

Iron-sensitive protein conjugates formed with a Wittig reaction precursor in ionic liquid

CHEMICAL COMMUNICATIONS, 59(81), 12160–12163.

Iron-sensitive protein conjugates formed with a Wittig reaction precursor in ionic liquid

Nizam, Z. M., Stowe, A. M., Mckinney, J. K., & Ohata, J. (2023, September 15). CHEMICAL COMMUNICATIONS, Vol. 9.

Small-Molecule CO₂ Donors Accelerate Three-Component Peptide/Protein Bioconjugation with Alkylazides and Phosphines in Ionic Liquids

Colella, B. M., & Ohata, J. (2023, December 18). SYNLETT, Vol. 12.

A puromycin-dependent activity-based sensing probe for histochemical staining of hydrogen peroxide in cells and animal tissues

Hoshi, K., Messina, M. S., Ohata, J., Chung, C. Y.-S., & Chang, C. J. (2022, May 13). NATURE PROTOCOLS, Vol. 5.

Correction to “An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine–Azide Bioconjugation Method”

Correction to “An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine–Azide Bioconjugation Method.” Journal of the American Chemical Society, 5.

Phosphine-Mediated Three-Component Bioconjugation of Amino- and Azidosaccharides in Ionic Liquids

Ohata, J., Hall, Y., Uzoewulu, C., Nizam, Z., Ishizawa, S., & El-Shaffey, H. (2022, April 18). (Vol. 4). Vol. 4.

Phosphine-mediated three-component bioconjugation of amino- and azidosaccharides in ionic liquids

Hall, Y. D., Uzoewulu, C. P., Nizam, Z. M., Ishizawa, S., El-Shaffey, H. M., & Ohata, J. (2022, August 19). CHEMICAL COMMUNICATIONS, Vol. 8.

Site-specific DNA functionalization through the tetrazene-forming reaction in ionic liquids

Ishizawa, S., Tumurkhuu, M., Gross, E. J., & Ohata, J. (2022, January 20). CHEMICAL SCIENCE, Vol. 1.

Site-specific DNA functionalization through the tetrazene-forming reaction in ionic liquids (vol 13, pg 1780, 2022)

Ishizawa, S., Tumurkhuu, M., Gross, E. J., & Ohata, J. (2022, June 7). CHEMICAL SCIENCE, Vol. 13, pp. 6749–6751.

Translation of a Phosphine- and Azide-Based Reaction to Chemical Modification of Biomolecules in Ionic Liquid

Uzoewulu, C. P., & Ohata, J. (2022, August 24). SYNLETT, Vol. 7.

Translation of a phosphine- and azide-based reaction to chemical modification of biomolecules in ionic liquid

Uzoewulu, C., & Ohata, J. (2022, July 11).

An Ionic Liquid Medium Enables Development of a Phosphine-Mediated Amine-Azide Bioconjugation Method

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143(33), 12974–12979.

Linear Hydrocarbon Chain Growth from a Molecular Diruthenium Carbide Platform

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 143(39), 16105–16112.

Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids

Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). (Vol. 9). Vol. 9.

Site-Specific DNA Functionalization through the Tetrazene-Forming Reaction in Ionic Liquids

Ishizawa, S., Tumurkhuu, M., Gross, E., & Ohata, J. (2021, September 13). (Vol. 9). Vol. 9.

An Activity-Based Methionine Bioconjugation Approach To Developing Proximity-Activated Imaging Reporters

ACS Central Science, 6(1), 32–40.

Activity-Based Sensing Methods for Monitoring the Reactive Carbon Species Carbon Monoxide and Formaldehyde in Living Systems

Accounts of Chemical Research.

An Activity-Based Methionine Bioconjugation Approach to Developing Proximity-Activated Imaging Reporters

Ohata, J., Krishnamoorthy, L., Gonzalez, M., Xiao, T., Iovan, D., Toste, F. D., … Chang, C. (2019, October 16). (Vol. 10). Vol. 10.

Metallvermittelte Funktionalisierung natürlicher Peptide und Proteine: Biokonjugation mit Übergangsmetallen

Angewandte Chemie, 131(19), 6238–6264.

Metal‐Mediated Functionalization of Natural Peptides and Proteins: Panning for Bioconjugation Gold

Angewandte Chemie International Edition, 58(19), 6176–6199.

Rapid nickel(ii)-promoted cysteine S-arylation with arylboronic acids

Chemical Communications.

A Naturally Encoded Dipeptide Handle for Bioorthogonal Chan-Lam Coupling

Angewandte Chemie International Edition, 57(15), 4015–4019.

A Three-Component Organometallic Tyrosine Bioconjugation

Angewandte Chemie International Edition, 57(11), 2827–2830.

Rhodium at the Chemistry-Biology Interface

Dalton Transactions.

A Hexa-rhodium Metallopeptide Catalyst for Site-Specific Functionalization of Natural Antibodies

Journal of the American Chemical Society, 139(36), 12617–12622.

Ascorbate as a pro-oxidant: mild N-terminal modification with vinylboronic acids

Chemical Communications, 53(10), 1622–1625.

Histidine-Directed Arylation/Alkenylation of Backbone N–H Bonds Mediated by Copper(II)

Journal of the American Chemical Society, 138(24), 7472–7475.

Convenient analysis of protein modification by chemical blotting with fluorogenic “click” reagents

Molecular BioSystems, 11(11), 2846–2849.

Luminogenic iridium azide complexes

Chemical Communications, 51(82), 15192–15195.

Potent and selective inhibition of SH3 domains with dirhodium metalloinhibitors

Chemical Science, 6(8), 4778–4783.

A Diruthenium μ-Carbido Complex That Shows Singlet-Carbene-like Reactivity

Journal of the American Chemical Society, 136(45), 15889–15892.