School of Science, Monash University, Bandar Sunway, Malaysia.
Anal Biochem. 2011 Jul 1;414(1):169-71. doi: 10.1016/j.ab.2011.03.006. Epub 2011 Mar 10.
The phage N15 protelomerase enzyme (TelN) is essential for the replication of its genome by resolution of its telRL domain, located within a telomerase occupancy site (tos), into hairpin telomeres. Isolation of TelN for in vitro processing of tos, however, is a highly complex process, requiring multiple purification steps. In this study a simplified protocol for crude total protein extraction is described that retains the tos-cleaving activity of TelN for at least 4 weeks, greatly simplifying in vitro testing of its activity. This protocol may be extended for functional analysis of other phage and bacterial proteins, particularly DNA-processing enzymes.
噬菌体 N15 端粒酶酶(TelN)对于其基因组的复制是必不可少的,通过其 telRL 结构域的分辨率来实现,该结构域位于端粒酶占据位点(tos)内,形成发夹状端粒。然而,为了进行 tos 的体外加工而分离 TelN 是一个高度复杂的过程,需要多个纯化步骤。在这项研究中,描述了一种简化的粗总蛋白提取方案,该方案至少在 4 周内保留了 TelN 对 tos 的切割活性,极大地简化了其活性的体外测试。该方案可扩展用于其他噬菌体和细菌蛋白的功能分析,特别是 DNA 加工酶。