Honarmand Ali, Mayall Robert, George Iain, Oberding Lisa, Dastidar Himika, Fegan Jamie, Chaudhuri Somshukla, Dole Justin, Feng Sharon, Hoang Denny, Moges Ruth, Osgood Julie, Remondini Taylor, van der Meulen Wm Keith, Wang Su, Wintersinger Chris, Zaparoli Zucoloto Amanda, Chatfield-Reed Kate, Arcellana-Panlilio Mayi, Nygren Anders
Department of Biological Sciences, University of Calgary , Calgary, Alberta T2N 1N4, Canada.
ACS Synth Biol. 2014 Dec 19;3(12):953-5. doi: 10.1021/sb500045w.
Transcription activator-like effectors (TALEs), originating from the Xanthomonas genus of bacteria, bind to specific DNA sequences based on amino acid sequence in the repeat-variable diresidue (RVD) positions of the protein. By altering these RVDs, it has been shown that a TALE protein can be engineered to bind virtually any DNA sequence of interest. The possibility of multiplexing TALEs for the purposes of identifying specific DNA sequences has yet to be explored. Here, we demonstrate a system in which a TALE protein bound to a nitrocellulose strip has been utilized to capture purified DNA, which is then detected using the binding of a second distinct TALE protein conjugated to a protein tag that is then detected by a dot blot. This system provides a signal only when both TALEs bind to their respective sequences, further demonstrating the specificity of the TALE binding.
转录激活样效应因子(TALEs)源自黄单胞菌属细菌,基于该蛋白质重复可变双残基(RVD)位置的氨基酸序列与特定DNA序列结合。通过改变这些RVD,已证明可对TALE蛋白进行工程改造,使其几乎能结合任何感兴趣的DNA序列。为识别特定DNA序列而对TALEs进行复用的可能性尚未得到探索。在此,我们展示了一种系统,其中与硝酸纤维素膜条结合的TALE蛋白被用于捕获纯化的DNA,然后使用与蛋白质标签偶联的第二种不同的TALE蛋白的结合进行检测,随后通过斑点印迹法进行检测。仅当两种TALEs都与其各自的序列结合时,该系统才会产生信号,进一步证明了TALE结合的特异性。