Sun H Q, Wooten D C, Janmey P A, Yin H L
Department of Physiology, University of Texas Southwestern Medical Center, Dallas 75235-9040.
J Biol Chem. 1994 Apr 1;269(13):9473-9.
Gelsolin is an actin filament-severing and -capping protein which is inhibited by polyphosphoinositides (PPI). Severing requires gelsolin binding to the side of the filaments through a site in segments 2 and 3 (S2-3) to position another site in segment 1 (S1) to sever filaments. In this paper, we report that S2-3, like S1, caps actin filaments. Since neither S1 and S2-3 caps as well as gelsolin, and neither severs actin filament, S2-3 may actively contribute to severing by capping filaments cooperatively with S1. We used deletional mutagenesis to locate the S2-3 sequence required for actin filament side binding, capping, and PPI binding and found that these sites are located close to the NH2 terminus of S2 (residues 161-172). S3, a segment which has no known function up to now and does not by itself bind actin, contributes to stable capping and may contain an additional PPI-binding site.
凝溶胶蛋白是一种肌动蛋白丝切断和封端蛋白,它受到多磷酸肌醇(PPI)的抑制。切断需要凝溶胶蛋白通过第2和第3片段(S2-3)中的一个位点与肌动蛋白丝的侧面结合,从而将第1片段(S1)中的另一个位点定位到切断肌动蛋白丝的位置。在本文中,我们报道S2-3与S1一样,能够封端肌动蛋白丝。由于S1和S2-3单独封端肌动蛋白丝的能力都不如凝溶胶蛋白,且都不能切断肌动蛋白丝,因此S2-3可能通过与S1协同封端肌动蛋白丝来积极促进切断过程。我们使用缺失诱变来定位肌动蛋白丝侧面结合、封端和PPI结合所需的S2-3序列,发现这些位点位于S2的NH2末端附近(第161-172位氨基酸)。S3是一个目前尚无已知功能且自身不结合肌动蛋白的片段,它有助于稳定封端,并且可能包含一个额外的PPI结合位点。