Proteins perform a variety of biological functions by interacting with different families of bimolecules. These interactions are largely noncovalent in nature. Although such noncovalent interactions provide diversity and dynamics for biology, their reversibility and weakness also impose strong limitations on researching and engineering protein-bimolecule interactions. In this application the natural barrier will be broken by designing and genetically incorporating bioreactive unnatural amino acids (Uaas) into proteins, which will enable proteins to bind with ribonucleic acids and carbohydrates in the covalent mode. The underlying innovation is to develop biocompatible chemistry, so that the Uaa will selectively react with the target ribonucleic acid or carbohydrate via proximity-enabled reactivity only upon binding, resulting in stable and irreversible linkage between protein and the target. To achieve these goals, new chemistries suitable for covalently targeting ribonucleic acids and carbohydrates in cellular and physiological conditions will be developed. The desired chemical functionality will be synthesized into the side chain of a Uaa, and the Uaa will be site-specifically incorporated into proteins in live cells via the genetic code expansion technology. This new covalent bonding strategy will be applied in live cells to understand RNA-protein recognition specificity, to identify substrate glycoproteins for glycosylation modifying enzymes, and to antagonize cell-cell communication. By harnessing the new covalent linkages inaccessible to natural proteins, this project will initiate a new dimension for researching and rationally engineering protein-RNA and protein-carbohydrate interactions. As such interactions are indispensable for biological functions and their aberrations are extensively implicated in various human diseases, new technologies resulting from this project will fundamentally impact both basic biological research and therapeutic applications.

Public Health Relevance

Statement We will develop an innovative method to expand the capabilities of proteins in living cells, which will provide new noninvasive tools for studying proteins, RNAs, and carbohydrates involved in various diseases. The success of this project will allow researchers to investigate challenging aspects of these molecules currently elusive to existing technologies.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM118384-05A1
Application #
10119770
Study Section
Enabling Bioanalytical and Imaging Technologies Study Section (EBIT)
Program Officer
Fabian, Miles
Project Start
2016-04-20
Project End
2024-06-30
Budget Start
2020-09-15
Budget End
2021-06-30
Support Year
5
Fiscal Year
2020
Total Cost
Indirect Cost
Name
University of California San Francisco
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
094878337
City
San Francisco
State
CA
Country
United States
Zip Code
94118
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Hoppmann, Christian; Wong, Allison; Yang, Bing et al. (2017) Site-specific incorporation of phosphotyrosine using an expanded genetic code. Nat Chem Biol 13:842-844
Klippenstein, Viktoria; Hoppmann, Christian; Ye, Shixin et al. (2017) Optocontrol of glutamate receptor activity by single side-chain photoisomerization. Elife 6:

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