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投射蛋白是一种无脊椎动物连接蛋白(肌联蛋白):从小龙虾爪肌中分离及其在小龙虾爪肌和昆虫飞行肌中的定位。

Projectin is an invertebrate connectin (titin): isolation from crayfish claw muscle and localization in crayfish claw muscle and insect flight muscle.

作者信息

Hu D H, Matsuno A, Terakado K, Matsuura T, Kimura S, Maruyama K

机构信息

Department of Biology, Faculty of Science, Chiba University, Japan.

出版信息

J Muscle Res Cell Motil. 1990 Dec;11(6):497-511. doi: 10.1007/BF01745217.

Abstract

A filamentous protein was isolated from crayfish claw muscle. This protein had physiochemical properties very similar to vertebrate skeletal muscle connectin (titin), although its apparent molecular mass (approximately 1200 kDa) was considerably lower than that of connectin (approximately 3000 kDa). Polyclonal as well as monoclonal antibodies against chicken skeletal muscle connectin reacted with the 1200 kDa protein from crayfish claw muscle. Conversely, polyclonal antibodies against crayfish 1200 kDa protein cross-reacted with chicken connectin. Circular dichroic spectra indicated the abundance of beta-sheet structure (approximately 60%). Low-angle shadowed images showed filamentous structures (0.2-0.5 microns) by electron microscopy. Proteolysis of the 1200 kDa protein by alpha-chymotrypsin or V8 protease rapidly resulted in formation of 1000 kDa or 1100 and 800 kDa peptides. The amino acid composition was very similar to those of vertebrate connectins and of honeybee flight muscle projectin. Based on the molecular weight and amino acid composition, the 1200 kDa protein is regarded to be crayfish projectin. Immunofluorescence and immunoelectron microscopy revealed that crayfish projectin was localized in the A/I junction area and A-band except for its centre region in crayfish claw muscles. Polyclonal antibodies against crayfish claw muscle projectin reacted with 1200 kDa projectin of honeybee and beetle flight muscle. A monoclonal antibody against chicken skeletal muscle connectin also reacted with honeybee and beetle projectin. Immunoelectron microscopic observations revealed that anti-crayfish projectin antibodies bound the connecting filaments linking the Z-line and the thick filaments up to the M-line of honeybee muscle sarcomere. Anti-crayfish projectin antibodies bound the I-band region near the Z-line of beetle flight muscle. It is concluded that the 1200 kDa projectin from crayfish claw muscle is an invertebrate connectin (titin). Recent work with locust flight muscle mini-titin (Nave & Weber, 1990) is in good agreement with the present study, except that the isolated mini-titin estimated as 600 kDa appears to be a proteolytic product (approximately 1100 kDa) of the parent molecule (approximately 1200 kDa).

摘要

从小龙虾爪肌中分离出一种丝状蛋白。这种蛋白的理化性质与脊椎动物骨骼肌连接蛋白(肌联蛋白)非常相似,尽管其表观分子量(约1200 kDa)明显低于连接蛋白(约3000 kDa)。抗鸡骨骼肌连接蛋白的多克隆抗体和单克隆抗体都能与小龙虾爪肌中的1200 kDa蛋白发生反应。相反,抗小龙虾1200 kDa蛋白的多克隆抗体与鸡连接蛋白发生交叉反应。圆二色光谱表明其富含β-折叠结构(约60%)。低角度投影图像通过电子显微镜显示出丝状结构(0.2 - 0.5微米)。用α-胰凝乳蛋白酶或V8蛋白酶对1200 kDa蛋白进行蛋白水解,迅速产生1000 kDa或1100 kDa和800 kDa的肽段。其氨基酸组成与脊椎动物连接蛋白以及蜜蜂飞行肌的肌动蛋白非常相似。基于分子量和氨基酸组成,1200 kDa蛋白被认为是小龙虾肌动蛋白。免疫荧光和免疫电子显微镜显示,小龙虾肌动蛋白定位于小龙虾爪肌的A/I交界区和A带,但不包括其中心区域。抗小龙虾爪肌肌动蛋白的多克隆抗体与蜜蜂和甲虫飞行肌的1200 kDa肌动蛋白发生反应。抗鸡骨骼肌连接蛋白的单克隆抗体也与蜜蜂和甲虫的肌动蛋白发生反应。免疫电子显微镜观察显示,抗小龙虾肌动蛋白抗体与连接Z线和粗肌丝直至蜜蜂肌节M线的连接丝结合。抗小龙虾肌动蛋白抗体与甲虫飞行肌Z线附近的I带区域结合。得出结论,小龙虾爪肌中的1200 kDa肌动蛋白是一种无脊椎动物连接蛋白(肌联蛋白)。最近对蝗虫飞行肌微肌联蛋白的研究(Nave & Weber,1990)与本研究结果高度一致,只是分离出的估计为600 kDa的微肌联蛋白似乎是母体分子(约1200 kDa)的蛋白水解产物(约1100 kDa)。

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