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Exploiting Endogenous Enzymes for Cancer-Cell Selective Metabolic Labeling of RNA in Vivo.
Beasley, Samantha; Vandewalle, Abigail; Singha, Monika; Nguyen, Kim; England, Whitney; Tarapore, Eric; Dai, Nan; Corrêa, Ivan R; Atwood, Scott X; Spitale, Robert C.
Affiliation
  • Beasley S; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
  • Vandewalle A; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
  • Singha M; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
  • Nguyen K; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
  • England W; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
  • Tarapore E; Department of Developmental & Cellular Biology, University of California─Irvine, Irvine, California 92697, United States.
  • Dai N; New England Biolabs, 240 County Road, Ipswich, Massachusetts 01938, United States.
  • Corrêa IR; New England Biolabs, 240 County Road, Ipswich, Massachusetts 01938, United States.
  • Atwood SX; Department of Developmental & Cellular Biology, University of California─Irvine, Irvine, California 92697, United States.
  • Spitale RC; Department of Pharmaceutical Sciences, University of California─Irvine, Irvine, California 92697, United States.
J Am Chem Soc ; 144(16): 7085-7088, 2022 04 27.
Article in En | MEDLINE | ID: mdl-35416650
Tissues and organs are composed of many diverse cell types, making cell-specific gene expression profiling a major challenge. Herein we report that endogenous enzymes, unique to a cell of interest, can be utilized to enable cell-specific metabolic labeling of RNA. We demonstrate that appropriately designed "caged" nucleosides can be rendered active by serving as a substrate for cancer-cell specific enzymes to enable RNA metabolic labeling, only in cancer cells. We envision that the ease and high stringency of our approach will enable expression analysis of tumor cells in complex environments.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA / Neoplasms Language: En Journal: J Am Chem Soc Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: RNA / Neoplasms Language: En Journal: J Am Chem Soc Year: 2022 Document type: Article Affiliation country: United States Country of publication: United States