Orthogonal Enzyme-Substrate Design Strategy for Discovery of Human Protein Palmitoyltransferase Substrates.
Orthogonal Enzyme-Substrate Design Strategy for Discovery of Human Protein Palmitoyltransferase Substrates.
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DOI:
10.1021/jacs.3c04359
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发表时间:
2023-10-18
影响因子:
15
通讯作者:
Banerjee, Anirban
中科院分区:
文献类型:
--
作者:
Puthenveetil, Robbins;Auger, Shelby A.;Gomez-Navarro, Natalia;Rana, Mitra Shumsher;Das, Riki;Healy, Liam Brendan;Suazo, Kiall F.;Shi, Zhen-Dan;Swenson, Rolf E.;Distefano, Mark D.;Banerjee, Anirban
Protein palmitoylation, with more than 5000 substrates, is the most prevalent form of protein lipidation. Palmitoylated proteins participate in almost all areas of cellular physiology and have been linked to several human diseases. Twenty-three zDHHC enzymes catalyze protein palmitoylation with extensive overlap among the substrates of each zDHHC member. Currently, there is no global strategy to delineate the physiological substrates of individual zDHHC enzymes without perturbing the natural cellular pool. Here, we outline a general approach to accomplish this on the basis of synthetic orthogonal substrates that are only compatible with engineered zDHHC enzymes. We demonstrate the utility of this strategy by validating known substrates and use it to identify novel substrates of two human zDHHC enzymes. Finally, we employ this method to discover and explore conserved palmitoylation in a family of host restriction factors against pathogenic viruses, including SARS-CoV-2.
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影响因子:
2.9
作者:
Hamel LD;Deschenes RJ;Mitchell DA
通讯作者:
Mitchell DA
DOI:
10.1126/science.aao6326
发表时间:
2018-01-12
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Rana MS;Kumar P;Lee CJ;Verardi R;Rajashankar KR;Banerjee A
通讯作者:
Banerjee A
影响因子:
15
作者:
Lin, Q;Jiang, FY;Gray, NS
通讯作者:
Gray, NS
DOI:
10.1007/978-1-4939-9532-5_16
发表时间:
2019-01-01
期刊:
PROTEIN LIPIDATION: METHODS AND PROTOCOLS
影响因子:
--
作者:
Blanc, Mathieu;David, Fabrice P. A.;van der Goot, F. Gisou
通讯作者:
van der Goot, F. Gisou
影响因子:
4.8
作者:
Lobo, S;Greentree, WK;Deschenes, RJ
通讯作者:
Deschenes, RJ