Millar A Harvey, Carrie Chris, Pogson Barry, Whelan James
Australian Research Council Centre of Excellence in Plant Energy Biology, University of Western Australia, Crawley 6009, Western Australia, Australia.
Plant Cell. 2009 Jun;21(6):1625-31. doi: 10.1105/tpc.109.066019. Epub 2009 Jun 26.
Defining the function of all proteins in an organism is one of the major objectives for biology in the coming decades. Here, we assess approaches used to determine subcellular protein location and discuss the relationship between protein location and function. It is important to recognize that targeting, accumulation, and the site of function are not necessarily interchangeable terms with respect to defining the location of a protein. Some proteins have tightly defined locations, whereas others have low specificity targeting and complex accumulation patterns. Location may be essential for function in some cases, but it may be much less important for other proteins. There is no single approach that can be considered entirely adequate for defining the in vivo location of all proteins. By combining approaches that assess targeting and accumulation of proteins, more confidence can be gained about localization. The strengths and weaknesses of different localization technologies are summarized, and some guidelines for performing combined targeting and accumulation assays are outlined.
确定生物体中所有蛋白质的功能是未来几十年生物学的主要目标之一。在此,我们评估用于确定亚细胞蛋白质定位的方法,并讨论蛋白质定位与功能之间的关系。必须认识到,就定义蛋白质的定位而言,靶向、积累和功能位点不一定是可互换的术语。一些蛋白质具有严格定义的定位,而另一些蛋白质具有低特异性靶向和复杂的积累模式。在某些情况下,定位对于功能可能至关重要,但对其他蛋白质而言可能不太重要。没有一种方法可以被认为完全足以定义所有蛋白质的体内定位。通过结合评估蛋白质靶向和积累的方法,可以对定位获得更多信心。总结了不同定位技术的优缺点,并概述了进行联合靶向和积累测定的一些指导原则。