Activity-based protein profiling: applications to biomarker discovery, in vivo imaging and drug discovery.

Alicia B Berger, Phillip M Vitorino, Matthew Bogyo
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引用次数: 132

Abstract

The genomic revolution has created a wealth of information regarding the fundamental genetic code that defines the inner workings of a cell. However, it has become clear that analyzing genome sequences alone will not lead to new therapies to fight human disease. Rather, an understanding of protein function within the context of complex cellular networks will be required to facilitate the discovery of novel drug targets and, subsequently, new therapies directed against them. The past ten years has seen a dramatic increase in technologies that allow large-scale, systems-based methods for analysis of global biological processes and disease states. In the field of proteomics, several well-established methods persist as a means to resolve and analyze complex mixtures of proteins derived from cells and tissues. However, the resolving power of these methods is often challenged by the diverse and dynamic nature of the proteome. The field of activity-based proteomics, or chemical proteomics, has been established in an attempt to focus proteomic efforts on subsets of physiologically important protein targets. This new approach to proteomics is centered around the use of small molecules termed activity-based probes (ABPs) as a means to tag, enrich, and isolate, distinct sets of proteins based on their enzymatic activity. Chemical probes can be 'tuned' to react with defined enzymatic targets through the use of chemically reactive warhead groups, fused to selective binding elements that control their overall specificity. As a result, ABPs function as highly specific, mechanism-based reagents that provide a direct readout of enzymatic activity within complex proteomes. Modification of protein targets by an ABP facilitates their purification and isolation, thereby eliminating many of the confounding issues of dynamic range in protein abundance. In this review, we outline recent advances in the field of chemical proteomics. Specifically, we highlight how this technology can be applied to advance the fields of biomarker discovery, in vivo imaging, and small molecule screening and drug target discovery.

基于活性的蛋白质分析:在生物标志物发现、体内成像和药物发现中的应用。
基因组革命创造了大量关于基本遗传密码的信息,这些信息定义了细胞的内部运作。然而,很明显,仅仅分析基因组序列并不能带来对抗人类疾病的新疗法。相反,在复杂的细胞网络背景下,蛋白质功能的理解将需要促进新的药物靶点的发现,并随后针对它们的新疗法。在过去的十年里,我们看到了技术的急剧增长,这些技术允许大规模的、基于系统的方法来分析全球生物过程和疾病状态。在蛋白质组学领域,一些成熟的方法仍然是解决和分析来自细胞和组织的复杂蛋白质混合物的一种手段。然而,这些方法的分辨能力经常受到蛋白质组的多样性和动态性的挑战。基于活性的蛋白质组学或化学蛋白质组学领域的建立是为了将蛋白质组学的研究重点放在生理上重要的蛋白质靶标的亚群上。这种蛋白质组学的新方法围绕着小分子的使用,称为基于活性的探针(ABPs),作为一种根据酶活性标记、富集和分离不同蛋白质集的手段。化学探针可以“调谐”,通过使用化学反应战斗部群,与控制其整体特异性的选择性结合元件融合,与确定的酶靶发生反应。因此,ABPs的功能是高度特异性的,基于机制的试剂,可以直接读出复杂蛋白质组中的酶活性。用ABP修饰蛋白靶标有助于它们的纯化和分离,从而消除了蛋白质丰度动态范围的许多混淆问题。本文综述了化学蛋白质组学研究的最新进展。具体来说,我们强调了这项技术如何应用于生物标志物发现、体内成像、小分子筛选和药物靶点发现等领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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