| Literature DB >> 31836350 |
Michaella J Levy1, David C Montgomery2, Mihaela E Sardiu1, Jose L Montano2, Sarah E Bergholtz2, Kellie D Nance2, Abigail L Thorpe2, Stephen D Fox3, Qishan Lin4, Thorkell Andresson3, Laurence Florens1, Michael P Washburn5, Jordan L Meier6.
Abstract
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 non-enzymatic 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. Published by Elsevier Ltd.Entities:
Keywords: acetyl-CoA; acetylation; acetyltransferase; activity-based protein profiling; chemical proteomics; epigenetics; malonylation; metabolism; pharmacology; systems biology
Year: 2019 PMID: 31836350 PMCID: PMC8237707 DOI: 10.1016/j.chembiol.2019.11.011
Source DB: PubMed Journal: Cell Chem Biol ISSN: 2451-9448 Impact factor: 8.116