Artalejo C R, Lemmon M A, Schlessinger J, Palfrey H C
Department of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208, USA.
EMBO J. 1997 Apr 1;16(7):1565-74. doi: 10.1093/emboj/16.7.1565.
Dynamin plays a key role in the scission event common to various types of endocytosis. We demonstrate that the pleckstrin homology (PH) domain of dynamin-1 is critical in the process of rapid endocytosis (RE) in chromaffin cells. Introduction of this isolated PH domain into cells at concentrations as low as 1 microM completely suppressed RE. PH domains from other proteins, including that from the closely related dynamin-2, were ineffective as inhibitors, even at high concentrations. Mutational studies indicated that a pair of isoform-specific amino acids, located in a variable loop between the first two beta-strands, accounted for the differential effect of the two dynamin PH domains. Switching these amino acids in the dynamin-2 PH domain to the equivalent residues in dynamin-1 (SL-->GI) generated a molecule that blocked RE. Thus, the PH domain of dynamin-1 is essential for RE and exhibits a precise molecular selectivity. As chromaffin cells express both dynamin-1 and -2, we speculate that different isoforms of dynamin may regulate distinct endocytotic processes and that the PH domain contributes to this specificity.
发动蛋白在各类内吞作用共有的缢断事件中起关键作用。我们证明,发动蛋白-1的普列克底物蛋白同源(PH)结构域在嗜铬细胞的快速内吞作用(RE)过程中至关重要。将这种分离的PH结构域以低至1微摩尔的浓度导入细胞,可完全抑制快速内吞作用。来自其他蛋白质的PH结构域,包括来自密切相关的发动蛋白-2的PH结构域,即使在高浓度下也无抑制作用。突变研究表明,位于前两条β链之间可变环中的一对亚型特异性氨基酸,解释了两种发动蛋白PH结构域的不同作用效果。将发动蛋白-2的PH结构域中的这些氨基酸替换为发动蛋白-1中的等效残基(SL→GI),产生了一种能阻断快速内吞作用的分子。因此,发动蛋白-1的PH结构域对快速内吞作用至关重要,并表现出精确的分子选择性。由于嗜铬细胞同时表达发动蛋白-1和-2,我们推测发动蛋白的不同亚型可能调节不同的内吞过程,且PH结构域促成了这种特异性。