共价蛋白质修饰:残基特异性亲电试剂的现状。

Covalent protein modification: the current landscape of residue-specific electrophiles.

机构信息

Department of Chemistry, Boston College, Chestnut Hill, MA 02467, United States.

Department of Chemistry, Boston College, Chestnut Hill, MA 02467, United States.

出版信息

Curr Opin Chem Biol. 2015 Feb;24:18-26. doi: 10.1016/j.cbpa.2014.10.021. Epub 2014 Nov 11.

Abstract

Functional amino acids that play critical roles in catalysis and regulation are known to display elevated nucleophilicity and can be selectively targeted for covalent modification by reactive electrophiles. Chemical-proteomic platforms, such as activity-based protein profiling (ABPP), exploit this reactivity by utilizing chemical probes to covalently modify active-site residues to inform on the functional state of enzymes within complex proteomes. These and other applications rely on the availability of a diverse array of electrophiles and detailed knowledge of the reactivity and amino-acid selectivity of these groups. Here, we survey the current landscape of electrophiles that covalently target various nucleophilic amino acids in proteins and highlight proteomic applications that have benefited from the unique properties of these electrophiles.

摘要

已知在催化和调节中起关键作用的功能性氨基酸具有较高的亲核性,可以被反应性亲电试剂选择性地靶向共价修饰。化学蛋白质组学平台,如基于活性的蛋白质分析(ABPP),利用这种反应性,通过使用化学探针共价修饰活性位点残基,从而了解复杂蛋白质组中酶的功能状态。这些和其他应用依赖于各种亲电试剂的可用性,以及对这些基团的反应性和氨基酸选择性的详细了解。在这里,我们调查了目前共价靶向蛋白质中各种亲核性氨基酸的亲电试剂,并强调了从这些亲电试剂的独特性质中受益的蛋白质组学应用。

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