Schnell D J, Kessler F, Blobel G
Department of Biological Sciences, Rutgers, State University of New Jersey, Newark 07102.
Science. 1994 Nov 11;266(5187):1007-12. doi: 10.1126/science.7973649.
Components of the protein import machinery of the chloroplast were isolated by a procedure in which the import machinery was engaged in vitro with a tagged import substrate under conditions that yielded largely chloroplast envelope-bound import intermediates. Subsequent detergent solubilization of envelope membranes showed that six envelope polypeptides copurified specifically and, apparently, stoichiometrically with the import intermediates. Four of these polypeptides are components of the outer membrane import machinery and are associated with early import intermediates. Two of these polypeptides have been characterized. One is a homolog of the heat shock protein hsp70; the other one is a channel-protein candidate.
叶绿体蛋白质输入机制的组成成分是通过一种方法分离出来的,在该方法中,输入机制在体外与带有标签的输入底物结合,条件是产生大量与叶绿体被膜结合的输入中间体。随后用去污剂溶解被膜,结果显示有六种被膜多肽与输入中间体特异性共纯化,而且显然是化学计量的。其中四种多肽是外膜输入机制的组成成分,并与早期输入中间体相关。其中两种多肽已得到鉴定。一种是热休克蛋白hsp70的同源物;另一种是通道蛋白候选物。