Kwiatkowski D J, Janmey P A, Yin H L
Hematology-Oncology Unit, Massachusetts General Hospital, Boston.
J Cell Biol. 1989 May;108(5):1717-26. doi: 10.1083/jcb.108.5.1717.
Gelsolin can sever actin filaments, nucleate actin filament assembly, and cap the fast-growing end of actin filaments. These functions are activated by Ca2+ and inhibited by polyphosphoinositides (PPI). We report here studies designed to delineate critical domains within gelsolin by deletional mutagenesis, using COS cells to secrete truncated plasma gelsolin after DNA transfection. Deletion of 11% of gelsolin from the COOH terminus resulted in a major loss of its ability to promote the nucleation step in actin filament assembly, suggesting that a COOH-terminal domain is important in this function. In contrast, derivatives with deletion of 79% of the gelsolin sequence exhibited normal PPI-regulated actin filament-severing activity. Combined with previous results using proteolytic fragments, we deduce that an 11-amino acid sequence in the COOH terminus of the smallest severing gelsolin derivative identified here mediates PPI-regulated binding of gelsolin to the sides of actin filaments before severing. Deletion of only 3% of gelsolin at the COOH terminus, including a dicarboxylic acid sequence similar to that found on the NH2 terminus of actin, resulted in a loss of Ca2+-requirement for filament severing and monomer binding. Since these residues in actin have been implicated as potential binding sites for gelsolin, our results raise the possibility that the analogous sequence at the COOH terminus of gelsolin may act as a Ca2+-regulated pseudosubstrate. However, derivatives with deletion of 69-79% of the COOH-terminal residues of gelsolin exhibited normal Ca2+ regulation of severing activity, establishing the intrinsic Ca2+ regulation of the NH2-terminal region. One or both mechanisms of Ca2+ regulation may occur in members of the gelsolin family of actin-severing proteins.
凝溶胶蛋白可以切断肌动蛋白丝,使肌动蛋白丝组装成核,并封闭肌动蛋白丝快速生长的末端。这些功能由Ca2+激活,并受到多磷酸肌醇(PPI)的抑制。我们在此报告了一些研究,旨在通过缺失诱变来描绘凝溶胶蛋白内的关键结构域,利用COS细胞在DNA转染后分泌截短的血浆凝溶胶蛋白。从COOH末端缺失11%的凝溶胶蛋白导致其促进肌动蛋白丝组装成核步骤的能力大幅丧失,这表明COOH末端结构域在该功能中很重要。相比之下,缺失79%凝溶胶蛋白序列的衍生物表现出正常的PPI调节的肌动蛋白丝切断活性。结合先前使用蛋白水解片段的结果,我们推断此处鉴定出的最小切断凝溶胶蛋白衍生物的COOH末端的11个氨基酸序列介导了凝溶胶蛋白在切断之前与肌动蛋白丝侧面的PPI调节结合。在COOH末端仅缺失3%的凝溶胶蛋白,包括一个与肌动蛋白NH2末端发现的二羧酸序列相似的序列,导致切断丝和单体结合对Ca2+的需求丧失。由于肌动蛋白中的这些残基被认为是凝溶胶蛋白的潜在结合位点,我们的结果提出了凝溶胶蛋白COOH末端类似序列可能作为Ca2+调节的假底物的可能性。然而,缺失凝溶胶蛋白COOH末端残基69 - 79%的衍生物表现出正常的Ca2+对切断活性的调节,确立了NH2末端区域固有的Ca2+调节。Ca2+调节的一种或两种机制可能发生在凝溶胶蛋白家族的肌动蛋白切断蛋白成员中。