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用于高通量蛋白质-蛋白质相互作用筛选的质量控制方法

Quality control methodology for high-throughput protein-protein interaction screening.

作者信息

Vazquez Alexei, Rual Jean-François, Venkatesan Kavitha

机构信息

Department of Radiation Oncology, The Cancer Institute of New Jersey and UMDNJ-Robert Wood Johnson Medical School, New Brunswick, NJ, USA.

出版信息

Methods Mol Biol. 2011;781:279-94. doi: 10.1007/978-1-61779-276-2_13.

Abstract

Protein-protein interactions are key to many aspects of the cell, including its cytoskeletal structure, the signaling processes in which it is involved, or its metabolism. Failure to form protein complexes or signaling cascades may sometimes translate into pathologic conditions such as cancer or neurodegenerative diseases. The set of all protein interactions between the proteins encoded by an organism constitutes its protein interaction network, representing a scaffold for biological function. Knowing the protein interaction network of an organism, combined with other sources of biological information, can unravel fundamental biological circuits and may help better understand the molecular basics of human diseases. The protein interaction network of an organism can be mapped by combining data obtained from both low-throughput screens, i.e., "one gene at a time" experiments and high-throughput screens, i.e., screens designed to interrogate large sets of proteins at once. In either case, quality controls are required to deal with the inherent imperfect nature of experimental assays. In this chapter, we discuss experimental and statistical methodologies to quantify error rates in high-throughput protein-protein interactions screens.

摘要

蛋白质-蛋白质相互作用是细胞多个方面的关键,包括其细胞骨架结构、所涉及的信号传导过程或新陈代谢。无法形成蛋白质复合物或信号级联有时可能转化为诸如癌症或神经退行性疾病等病理状况。生物体编码的蛋白质之间所有蛋白质相互作用的集合构成其蛋白质相互作用网络,代表着生物学功能的支架。了解生物体的蛋白质相互作用网络,结合其他生物学信息来源,可以揭示基本的生物回路,并可能有助于更好地理解人类疾病的分子基础。生物体的蛋白质相互作用网络可以通过结合从低通量筛选(即“一次一个基因”实验)和高通量筛选(即旨在一次性检测大量蛋白质的筛选)获得的数据来绘制。在任何一种情况下,都需要质量控制来处理实验分析固有的不完美性质。在本章中,我们将讨论用于量化高通量蛋白质-蛋白质相互作用筛选中错误率的实验和统计方法。

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