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在意外位置对多任务蛋白进行蛋白质组学鉴定会使药物靶向变得复杂。

Proteomic identification of multitasking proteins in unexpected locations complicates drug targeting.

作者信息

Butler Georgina S, Overall Christopher M

机构信息

Centre for Blood Research, Department of Oral Biological and Medical Sciences, University of British Columbia, Vancouver, British Columbia, VT6 1Z3, Canada.

出版信息

Nat Rev Drug Discov. 2009 Dec;8(12):935-48. doi: 10.1038/nrd2945.

Abstract

Proteomics has revealed that many proteins are present in unexpected cellular locations. Moreover, it is increasingly recognized that proteins can translocate between intracellular and extracellular compartments in non-conventional ways. This increases gene pleiotrophy as the diverse functions of the protein that the gene encodes are dependent on the cellular location. Given that trafficking drug targets may exist in various forms--often with completely different functions--in multiple cellular compartments, careful interpretation of proteomics data is needed for an accurate understanding of gene function. This Perspective is intended to inspire the investigation of unusual protein localizations, rather than assuming that they are due to mislocalization or artefacts. Given a fair chance, proteomics could reveal novel and unforeseen biology with important ramifications for target validation in drug discovery.

摘要

蛋白质组学研究表明,许多蛋白质存在于意想不到的细胞位置。此外,人们越来越认识到,蛋白质可以通过非常规方式在细胞内和细胞外区室之间转运。这增加了基因的多效性,因为基因编码的蛋白质的多种功能取决于细胞位置。鉴于转运药物靶点可能以多种形式存在——通常具有完全不同的功能——存在于多个细胞区室中,因此需要仔细解读蛋白质组学数据,才能准确理解基因功能。本观点旨在激发对异常蛋白质定位的研究,而不是假定它们是由于定位错误或人为因素造成的。如果有适当的机会,蛋白质组学可能会揭示新的、意想不到的生物学现象,这对药物发现中的靶点验证具有重要意义。

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