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利用酵母三杂交系统克隆桥梁蛋白。

Use of a yeast three-hybrid system to clone bridging proteins.

作者信息

Zhang J

机构信息

Guilford Pharmaceuticals, Inc., Baltimore, Maryland 21224, USA.

出版信息

Methods Enzymol. 2000;328:103-10. doi: 10.1016/s0076-6879(00)28393-6.

Abstract

The three-hybrid system described here should facilitate screening cDNA libraries to clone "bridging" proteins in ternary complex. The pDela constructs were initially designed to be compatible with the Gal4-based two-hybrid system, such as pGAD424/pGBT9. The Ura selection offered by pDela makes it easy to introduce the "bridging" protein into the yeast containing the other two hybrids, the BD fusion protein and the AD fusion protein. Because many of the widely used two-hybrid systems employ Trp-, Leu-, His-, or ziocin selection in the shuttle vectors, the Ura(+)-based pDela constructs can be used directly in those systems.

摘要

本文所述的三杂交系统应有助于筛选cDNA文库,以克隆三元复合物中的“桥梁”蛋白。pDela构建体最初设计为与基于Gal4的双杂交系统兼容,如pGAD424/pGBT9。pDela提供的尿嘧啶选择使得将“桥梁”蛋白引入含有其他两种杂交体(BD融合蛋白和AD融合蛋白)的酵母中变得容易。由于许多广泛使用的双杂交系统在穿梭载体中采用色氨酸、亮氨酸、组氨酸或紫霉素选择,基于尿嘧啶(+)的pDela构建体可直接用于这些系统。

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