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SNAP展示:微滴中的体外蛋白质进化

SNAP display: in vitro protein evolution in microdroplets.

作者信息

Kaltenbach Miriam, Hollfelder Florian

机构信息

Department of Biochemistry, University of Cambridge, Cambridge, UK.

出版信息

Methods Mol Biol. 2012;805:101-11. doi: 10.1007/978-1-61779-379-0_7.

Abstract

SNAP display is based on the covalent reaction of the DNA repair protein AGT (O(6)-alkylguanine DNA alkyltransferase, the "SNAP-tag") with its substrate benzylguanine (BG). Linear, BG-labelled template DNA is encapsulated in water-in-oil emulsion droplets with a diameter of a few micrometres (i.e. 1 mL of emulsion contains ∼10(10) compartments). Each droplet contains only a single DNA copy, which is transcribed and translated in vitro. The expressed AGT fusion proteins attach to their coding DNA via the BG label inside the droplet, which ensures that a specific genotype-phenotype linkage is established. Subsequently, the emulsion is broken and protein-DNA conjugates, which constitute a DNA-tagged protein library, selected via affinity panning. This method will prove a useful addition to the array of in vitro display systems, distinguished by the stability of DNA as the coding nucleic acid and the covalent link between gene and protein.

摘要

SNAP展示基于DNA修复蛋白AGT(O(6)-烷基鸟嘌呤DNA烷基转移酶,即“SNAP标签”)与其底物苄基鸟嘌呤(BG)的共价反应。线性的、BG标记的模板DNA被封装在直径为几微米的油包水乳液滴中(即1 mL乳液包含约10(10)个隔室)。每个液滴仅包含一个DNA拷贝,该拷贝在体外进行转录和翻译。表达的AGT融合蛋白通过液滴内的BG标签附着于其编码DNA,这确保了建立特定的基因型-表型联系。随后,乳液被打破,构成DNA标记蛋白文库的蛋白质-DNA缀合物通过亲和淘选进行筛选。该方法将被证明是体外展示系统阵列中的一个有用补充,其特点是DNA作为编码核酸的稳定性以及基因与蛋白质之间的共价连接。

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