Kaltenbach Miriam, Hollfelder Florian
Department of Biochemistry, University of Cambridge, Cambridge, UK.
Methods Mol Biol. 2012;805:101-11. doi: 10.1007/978-1-61779-379-0_7.
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.
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。