Rees David M, Willhoft Oliver, Lin Chia-Liang, Bythell-Douglas Rohan, Wigley Dale B
Section of Structural Biology, Imperial College London, London, United Kingdom.
Section of Structural Biology, Imperial College London, London, United Kingdom.
Methods Enzymol. 2017;592:27-47. doi: 10.1016/bs.mie.2017.03.015. Epub 2017 Apr 17.
We have developed a novel system to facilitate the rapid and easy cloning of multiple genes (>10) in under a week. Using this system we have been able to successfully clone, overexpress, and purify a number of large multimeric proteins from insect cells, including the chromatin remodeling complexes SWR1 and INO80. Using Förster resonance energy transfer (FRET)-based assays we have demonstrated that our overexpressed enzymes have activities comparable to those purified from sources where the proteins are expressed under their endogenous promoters.
我们开发了一种新型系统,可在一周内快速简便地克隆多个(>10个)基因。利用该系统,我们已成功从昆虫细胞中克隆、过表达并纯化了多种大型多聚体蛋白,包括染色质重塑复合物SWR1和INO80。通过基于荧光共振能量转移(FRET)的检测,我们证明了我们过表达的酶的活性与从在其内源启动子下表达蛋白质的来源中纯化得到的酶的活性相当。