Vergis James M, Wiener Michael C
Department of Molecular Physiology and Biological Physics, University of Virginia, 480 Ray C. Hunt Drive, Charlottesville, VA 22908, USA.
Protein Expr Purif. 2011 Aug;78(2):139-42. doi: 10.1016/j.pep.2011.04.011. Epub 2011 Apr 24.
Recombinant proteins typically include one or more affinity tags to facilitate purification and/or detection. Expression constructs with affinity tags often include an engineered protease site for tag removal. Like other enzymes, the activities of proteases can be affected by buffer conditions. The buffers used for integral membrane proteins contain detergents, which are required to maintain protein solubility. We examined the detergent sensitivity of six commonly-used proteases (enterokinase, factor Xa, human rhinovirus 3C protease, SUMOstar, tobacco etch virus protease, and thrombin) by use of a panel of 94 individual detergents. Thrombin activity was insensitive to the entire panel of detergents, thus suggesting it as the optimal choice for use with membrane proteins. Enterokinase and factor Xa were only affected by a small number of detergents, making them good choices as well.
重组蛋白通常包含一个或多个亲和标签,以促进纯化和/或检测。带有亲和标签的表达构建体通常包含一个用于去除标签的工程化蛋白酶位点。与其他酶一样,蛋白酶的活性会受到缓冲液条件的影响。用于整合膜蛋白的缓冲液含有去污剂,这是维持蛋白质溶解性所必需的。我们使用一组94种单独的去污剂,检测了六种常用蛋白酶(肠激酶、凝血因子Xa、人鼻病毒3C蛋白酶、SUMOstar、烟草蚀纹病毒蛋白酶和凝血酶)对去污剂的敏感性。凝血酶活性对整个去污剂组不敏感,因此表明它是用于膜蛋白的最佳选择。肠激酶和凝血因子Xa仅受到少数去污剂的影响,因此它们也是不错的选择。