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蛋白质结构域微阵列作为一个平台来破解信号通路和组蛋白密码。

Protein domain microarrays as a platform to decipher signaling pathways and the histone code.

机构信息

Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, TX 78957, USA; Graduate Program in Genetics & Epigenetics, The University of Texas MD Anderson Cancer Center UTHealth Graduate School of Biomedical Sciences, Houston, TX 77030, USA.

Department of Epigenetics and Molecular Carcinogenesis, The University of Texas MD Anderson Cancer Center, Smithville, TX 78957, USA.

出版信息

Methods. 2020 Dec 1;184:4-12. doi: 10.1016/j.ymeth.2019.08.007. Epub 2019 Aug 23.

Abstract

Signal transduction is driven by protein interactions that are controlled by posttranslational modifications (PTM). Usually, protein domains are responsible for "reading" the PTM signal deposited on the interacting partners. Protein domain microarrays have been developed as a high throughput platform to facilitate the rapid identification of protein-protein interactions, and this approach has become broadly used in biomedical research. In this review, we will summarize the history, development and applications of this technique, including the use of protein domain microarrays in identifying both novel protein-protein interactions and small molecules that block these interactions. We will focus on the approaches we use in the Protein Array and Analysis Core - the PAAC - at MD Anderson Cancer Center. We will also address the technical limitations and discuss future directions.

摘要

信号转导是由受翻译后修饰(PTM)控制的蛋白质相互作用驱动的。通常,蛋白质结构域负责“读取”沉积在相互作用伙伴上的 PTM 信号。蛋白质结构域微阵列已被开发为高通量平台,以促进蛋白质-蛋白质相互作用的快速鉴定,并且该方法已广泛用于生物医学研究。在这篇综述中,我们将总结该技术的历史、发展和应用,包括使用蛋白质结构域微阵列鉴定新的蛋白质-蛋白质相互作用以及阻断这些相互作用的小分子。我们将重点介绍 MD 安德森癌症中心蛋白质阵列和分析核心(PAAC)中使用的方法。我们还将讨论技术限制并探讨未来方向。

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