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基于活性的蛋白质谱分析:功能蛋白质组学的新进展与新方向。

Activity-based protein profiling: new developments and directions in functional proteomics.

作者信息

Uttamchandani Mahesh, Li Junqi, Sun Hongyan, Yao Shao Q

机构信息

Defence Medical and Environmental Research Institute, DSO National Laboratories, 27 Medical Drive, Singapore 117510, Singapore.

出版信息

Chembiochem. 2008 Mar 25;9(5):667-75. doi: 10.1002/cbic.200700755.

Abstract

Proteomic screening has become increasingly insightful with the availability of novel analytical tools and technologies. Detailed analysis and integration of the profound datasets attained from comprehensive profiling studies are enabling researchers to dig deeper into the foundations of genomic and proteomic networks, towards a clearer understanding of the intricate cellular circuitries they manifest. The major difficulty often lies in correlating the patho/physiological state presented with the underlying biological mechanisms; therefore, identification of causal variants as therapeutic targets is extremely important. Herein, we will describe methods that address this challenge through activity-based protein profiling, which applies chemical probes to the comparison and monitoring of protein dynamics across complex proteomes. Over recent years such activity-based probes have been creatively augmented with applications in gel-based separations, microarrays and in vivo imaging. These developments offer a newfound ability to characterise and differentiate cells, tissues and proteomes through activity-dependent signatures; this has expanded the scope and impact of activity-based probes in biomedical research.

摘要

随着新型分析工具和技术的出现,蛋白质组学筛选变得越来越有洞察力。对从全面分析研究中获得的大量数据集进行详细分析和整合,使研究人员能够更深入地探究基因组和蛋白质组网络的基础,从而更清楚地了解它们所呈现的复杂细胞通路。主要困难往往在于将呈现的病理/生理状态与潜在的生物学机制联系起来;因此,识别作为治疗靶点的因果变异极其重要。在此,我们将描述通过基于活性的蛋白质谱分析来应对这一挑战的方法,该方法应用化学探针来比较和监测复杂蛋白质组中的蛋白质动态。近年来,这种基于活性的探针在基于凝胶的分离、微阵列和体内成像等应用中得到了创造性的扩展。这些进展提供了一种通过活性依赖特征来表征和区分细胞、组织和蛋白质组的新能力;这扩大了基于活性的探针在生物医学研究中的范围和影响。

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