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基于DNA片段化的可溶性蛋白质表达组合方法 第一部分:生成DNA片段文库

DNA fragmentation-based combinatorial approaches to soluble protein expression Part I. Generating DNA fragment libraries.

作者信息

Prodromou Chrisostomos, Savva Renos, Driscoll Paul C

机构信息

Section of Structural Biology, Institute of Cancer Research, Chester Beatty Laboratories, 237 Fulham Road, London SW3 6JB, United Kingdom.

出版信息

Drug Discov Today. 2007 Nov;12(21-22):931-8. doi: 10.1016/j.drudis.2007.08.012. Epub 2007 Oct 23.

Abstract

In addressing a new drug discovery target, the generation of tractable protein substrates for functional and structural analyses can represent a significant hurdle. Traditional approaches rely on protein expression trials of multiple variants in various systems, frequently with limited success. The increasing knowledge base derived from genomics and structural proteomics initiatives assists the bioinformatics-led design of these experiments. Nevertheless, for many eukaryotic polypeptides, particularly those with relatively few homologues, the generation of useful protein products can still be a major challenge. This review describes the basis of efforts to forge an alternative 'domain-hunting' paradigm, based upon combinatorial sampling of expression construct libraries derived by fragmentation of the encoding DNA template, namely the methods and considerations in generating fragment length DNA from target genes. An accompanying review focuses upon the expression screening of such combinatorial DNA libraries for the sampling of the corresponding set of protein fragments.

摘要

在确定新药研发靶点时,生成用于功能和结构分析的易处理蛋白质底物可能是一个重大障碍。传统方法依赖于在各种系统中对多个变体进行蛋白质表达试验,但成功率往往有限。来自基因组学和结构蛋白质组学计划的知识储备不断增加,有助于以生物信息学为主导设计这些实验。然而,对于许多真核生物多肽,尤其是那些同源物相对较少的多肽,生成有用的蛋白质产物仍然可能是一项重大挑战。本综述描述了基于对编码DNA模板进行片段化衍生的表达构建体文库进行组合采样,即从靶基因生成片段长度DNA的方法和注意事项,打造另一种“结构域搜寻”模式的努力基础。一篇配套综述重点关注此类组合DNA文库的表达筛选,以对相应的蛋白质片段集进行采样。

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