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通过羧基端尾端蛋白质组分析(C-TAILS)鉴定癌症中的蛋白酶切割位点和底物

Identification of Protease Cleavage Sites and Substrates in Cancer by Carboxy-TAILS (C-TAILS).

作者信息

Solis Nestor, Overall Christopher M

机构信息

Department of Oral Biological and Medical Sciences, Faculty of Dentistry, University of British Columbia, Vancouver, BC, Canada.

Centre for Blood Research, University of British Columbia, Vancouver, BC, Canada.

出版信息

Methods Mol Biol. 2018;1731:15-28. doi: 10.1007/978-1-4939-7595-2_2.

Abstract

Determination of drug targets and development of novel therapeutics for the treatment of different cancers are actively ongoing areas of research. Proteases being the second largest group of enzymes in humans present themselves as attractive targets for blocking and activation to treat malignancies. However, determination of the protease cleavage substrates is often missed by utilizing conventional modern proteomic approaches. The relatively low abundance of proteolytically processed, and mostly semi-tryptic, peptides compared to tryptic peptides generated in shotgun proteomics compounded with their poorer identification rates makes the identification of such critical peptides challenging and so are mostly overlooked. Our laboratory introduced Terminal Amine Isotopic Labeling of Substrates (TAILS) to identify N-terminal peptides from cleavage events. In this chapter we present a protocol from our complementary method carboxy-TAILS (C-TAILS) to identify C-terminal peptides in metabolically labeled cancer cell lines.

摘要

确定药物靶点以及开发用于治疗不同癌症的新型疗法是当前积极开展的研究领域。蛋白酶作为人类第二大类酶,是阻断和激活以治疗恶性肿瘤的有吸引力的靶点。然而,利用传统的现代蛋白质组学方法往往会遗漏蛋白酶切割底物的确定。与鸟枪法蛋白质组学中产生的胰蛋白酶肽相比,经蛋白水解处理的、大多为半胰蛋白酶的肽丰度相对较低,再加上其较低的鉴定率,使得鉴定此类关键肽具有挑战性,因此大多被忽视。我们实验室引入了底物末端胺同位素标记法(TAILS)来鉴定切割事件中的N端肽。在本章中,我们介绍了我们的互补方法羧基-TAILS(C-TAILS)的方案,用于鉴定代谢标记的癌细胞系中的C端肽。

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