4.5 Article

A Systems Chemoproteomic Analysis of Acyl-CoA/Protein Interaction Networks

Journal

CELL CHEMICAL BIOLOGY
Volume 27, Issue 3, Pages 322-+

Publisher

CELL PRESS
DOI: 10.1016/j.chembiol.2019.11.011

Keywords

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Funding

  1. Intramural Research Program of the NIH, National Cancer Institute, Center for Cancer Research [ZIA BC011488-04]
  2. Stowers Institute for Medical Research
  3. National Institute of General Medical Sciences of the National Institutes of Health [RO1GM112639]
  4. National Cancer Institute, National Institutes of Health [HHSN261200800001E]
  5. NATIONAL CANCER INSTITUTE [ZIABC011488] Funding Source: NIH RePORTER

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Acyl-coenzyme A (CoA)/protein interactions are essential for life. Despite this importance, their global scope and selectivity remains undefined. Here, we describe CATNIP (CoA/AcetylTraNsferase Interaction Profiling), a chemoproteomic platform for the high-throughput analysis of acyl-CoA/protein interactions in endogenous proteomes. First, we apply CATNIP to identify acetyl-CoA-binding proteins through unbiased clustering of competitive dose-response data. Next, we use this method to profile the selectivity of acyl-CoA/protein interactions, leading to the identification of specific acyl-CoA engagement signatures. Finally, we apply systems-level analyses to assess the features of protein networks that may interact with acyl-CoAs, and use a strategy for high-confidence proteomic annotation of acetyl-CoA-binding proteins to identify a site of nonenzymatic acylation in the NAT10 acetyltransferase domain that is likely driven by acyl-CoA binding. Overall, our studies illustrate how chemoproteomics and systems biology can be integrated to understand the roles of acyl-CoA metabolism in biology and disease.

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