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膜蛋白靶向绝对定量的当前方法与挑战

Current approaches and challenges in targeted absolute quantification of membrane proteins.

作者信息

Trötschel Christian, Poetsch Ansgar

机构信息

Department of Plant Biochemistry, Ruhr-University Bochum, Bochum, Germany.

出版信息

Proteomics. 2015 Mar;15(5-6):915-29. doi: 10.1002/pmic.201400427. Epub 2015 Jan 21.

DOI:10.1002/pmic.201400427
PMID:25490887
Abstract

Experimental determination of absolute protein amounts is becoming increasingly important for the establishment and validation of biomarkers, and systems biology approaches aimed at a quantitative description of a biological process. Residing at compartmental or cellular barriers, and acting as prominent drug targets, integral membranes proteins, being completely embedded in the lipid bilayer, possess characteristic physicochemical properties and are often in low abundance. These features challenge the quantification with targeted MS and the ability to accurately determine the amount of membrane proteins with high sensitivity. This review summarizes the current status of targeted membrane protein quantification with emphasis on sample preparation beforehand MS. From the beginning to the end of a usual sample preparation workflow, consisting essentially of reference point selection, cell lysis, digestion, and addition of suitable isotope-labeled standards, general and particular challenges for membrane proteins will be discussed step by step. Based on the presentation of current achievements, possible measures to better address these challenges and future avenues of targeted membrane proteomics are presented.

摘要

对于生物标志物的建立和验证以及旨在对生物过程进行定量描述的系统生物学方法而言,绝对蛋白量的实验测定变得越来越重要。整合膜蛋白位于区室或细胞屏障处,作为重要的药物靶点,它们完全嵌入脂质双层中,具有独特的物理化学性质,且丰度往往较低。这些特性对靶向质谱定量以及高灵敏度准确测定膜蛋白量的能力构成了挑战。本综述总结了靶向膜蛋白定量的现状,重点是质谱分析前的样品制备。从通常的样品制备工作流程的开始到结束,该流程主要包括参考点选择、细胞裂解、消化以及添加合适的同位素标记标准品,将逐步讨论膜蛋白面临的一般和特殊挑战。基于当前成果的介绍,提出了更好应对这些挑战的可能措施以及靶向膜蛋白质组学的未来发展方向。

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Current approaches and challenges in targeted absolute quantification of membrane proteins.膜蛋白靶向绝对定量的当前方法与挑战
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