Chaponnier C, Goethals M, Janmey P A, Gabbiani F, Gabbiani G, Vandekerckhove J
Department of Pathology, University of Geneva, Switzerland.
J Cell Biol. 1995 Aug;130(4):887-95. doi: 10.1083/jcb.130.4.887.
The blocking effect of the NH2-terminal decapeptide of alpha-smooth muscle (SM) actin AcEEED-STALVC on the binding of the specific monoclonal antibody anti-alpha SM-1 (Skalli, O., P. Ropraz, A. Trzeviak, G. Benzonana, D. Gillessen, and G. Gabbiani. 1986. J. Cell Biol. 103:2787-2796) was compared with that of synthetic peptides modified by changing the acetyl group or by substituting an amino acid in positions 1 to 5. Using immunofluorescence and immunoblotting techniques, anti-alpha SM-1 binding was abolished by the native peptide and by peptides with a substitution in position 5, indicating that AcEEED is the epitope for anti-alpha SM-1. Incubation of anti-alpha SM-1 (or of its Fab fragment) with arterial SM actin increased polymerization in physiological salt conditions; the antibody binding did not hinder the incorporation of the actin antibody complex into the filaments. This action was not exerted on skeletal muscle actin. After microinjection of the alpha-SM actin NH2-terminal decapeptide or of the epitopic peptide into cultured aortic smooth muscle cells, double immunofluorescence for alpha-SM actin and total actin showed a selective disappearance of alpha-SM actin staining, detectable at approximately 30 min. When a control peptide (e.g. alpha-skeletal [SK] actin NH2-terminal peptide) was microinjected, this was not seen. This effect is compatible with the possibility that the epitopic peptide traps a protein involved in alpha-SM actin polymerization during the dynamic filament turnover in stress fibers. Whatever the mechanism, this is the first evidence that the NH2 terminus of an actin isoform plays a role in the regulation of polymerization in vitro and in vivo.
比较了α-平滑肌(SM)肌动蛋白AcEEED-STALVC的氨基末端十肽对特异性单克隆抗体抗α SM-1(Skalli,O.,P. Ropraz,A. Trzeviak,G. Benzonana,D. Gillessen和G. Gabbiani。1986年。《细胞生物学杂志》103:2787 - 2796)结合的阻断作用与通过改变乙酰基或替换第1至5位氨基酸而修饰的合成肽的阻断作用。使用免疫荧光和免疫印迹技术,天然肽以及第5位有替换的肽消除了抗α SM-1的结合,表明AcEEED是抗α SM-1的表位。在生理盐条件下,抗α SM-1(或其Fab片段)与动脉SM肌动蛋白的孵育增加了聚合作用;抗体结合并不阻碍肌动蛋白抗体复合物掺入细丝中。这种作用对骨骼肌肌动蛋白不产生。将α-SM肌动蛋白氨基末端十肽或表位肽显微注射到培养的主动脉平滑肌细胞中后,对α-SM肌动蛋白和总肌动蛋白的双重免疫荧光显示α-SM肌动蛋白染色选择性消失,约30分钟时可检测到。当显微注射对照肽(例如α-骨骼肌[SK]肌动蛋白氨基末端肽)时,未观察到这种情况。这种效应与表位肽在应力纤维中动态细丝周转期间捕获参与α-SM肌动蛋白聚合的蛋白质的可能性相符。无论机制如何,这是肌动蛋白异构体的氨基末端在体外和体内聚合调节中起作用的首个证据。