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异步飞行肌的肌钙蛋白

Troponin of asynchronous flight muscle.

作者信息

Bullard B, Leonard K, Larkins A, Butcher G, Karlik C, Fyrberg E

机构信息

Department of Immunology, AFRC Institute of Animal Physiology and Genetics Research, Babraham, Cambridge, U.K.

出版信息

J Mol Biol. 1988 Dec 5;204(3):621-37. doi: 10.1016/0022-2836(88)90360-9.

Abstract

Troponin has been prepared from the asynchronous flight muscle of Lethocerus (water bug) taking special care to prevent proteolysis. The regulatory complex contained tropomyosin and troponin components. The troponin components were Tn-C (18,000 Mr), Tn-T (apparent Mr 53,000) and a heavy component, Tn-H (apparent Mr 80,000). The troponin was tightly bound to tropomyosin and could not be dissociated from it in non-denaturing conditions. A complex of Tn-T, Tn-H and tropomyosin inhibited actomyosin ATPase activity and the inhibition was relieved by Tn-C from vertebrate striated muscle in the presence of Ca2+. However, unlike vertebrate Tn-I, Tn-H by itself was not inhibitory. Monoclonal antibodies were obtained to Tn-T and Tn-H. Antibody to Tn-T was used to screen an expression library of Drosophila cDNA cloned in lambda phage. The sequence of cDNA coding for the protein was determined and hence the amino acid sequence. The Drosophila protein has a sequence similar to that of vertebrate skeletal and cardiac Tn-T. The sequence extends beyond the carboxyl end of the vertebrate sequences, and the last 40 residues are acidic. Part of the sequence of Drosophila Tn-T is homologous to the carboxyl end of the Drosophila myosin light chain MLC-2 and one anti-Tn-T antibody cross-reacted with the light chain. Lethocerus Tn-H is related to the large tropomyosins of Drosophila flight muscle, for which the amino acid sequence is known, since antibodies that recognize this component also recognize the large tropomyosins. Tn-H is easily digested by calpain, suggesting that part of the molecule has an extended configuration. Electron micrographs of negatively stained specimens showed that Lethocerus thin filaments have projections at about 39 nm intervals, which are not seen on thin filaments from vertebrate striated muscle and are probably due to the relatively large troponin complex. Decoration of the thin filaments with myosin subfragment-1 in rigor conditions appeared not to be affected by the troponin. The troponin of asynchronous flight muscle lacks the Tn-I component of vertebrate striated muscle. Tn-H occurs only in the flight muscle and may be involved in the activation of this muscle by stretch.

摘要

肌钙蛋白是从大田鳖(水蝽)的异步飞行肌中制备的,制备过程中特别注意防止蛋白水解。调节复合物包含原肌球蛋白和肌钙蛋白成分。肌钙蛋白成分包括肌钙蛋白C(18,000道尔顿)、肌钙蛋白T(表观分子量53,000)和一个重成分,即肌钙蛋白H(表观分子量80,000)。肌钙蛋白与原肌球蛋白紧密结合,在非变性条件下无法与之解离。肌钙蛋白T、肌钙蛋白H和原肌球蛋白的复合物抑制了肌动球蛋白ATP酶活性,在钙离子存在的情况下,脊椎动物横纹肌的肌钙蛋白C可解除这种抑制作用。然而,与脊椎动物的肌钙蛋白I不同,肌钙蛋白H本身并无抑制作用。获得了针对肌钙蛋白T和肌钙蛋白H的单克隆抗体。用针对肌钙蛋白T的抗体筛选克隆于λ噬菌体中的果蝇cDNA表达文库。确定了编码该蛋白的cDNA序列,进而确定了氨基酸序列。果蝇蛋白的序列与脊椎动物骨骼肌和心肌的肌钙蛋白T序列相似。该序列延伸至脊椎动物序列的羧基末端之外,最后40个残基呈酸性。果蝇肌钙蛋白T的部分序列与果蝇肌球蛋白轻链MLC-2的羧基末端同源,一种抗肌钙蛋白T抗体与轻链发生交叉反应。大田鳖肌钙蛋白H与已知氨基酸序列的果蝇飞行肌的大原肌球蛋白相关,因为识别该成分的抗体也能识别大原肌球蛋白。肌钙蛋白H很容易被钙蛋白酶消化,这表明分子的一部分具有伸展的构象。负染标本的电子显微镜照片显示,大田鳖的细肌丝每隔约39纳米有突起,在脊椎动物横纹肌的细肌丝上未见这种突起,这可能是由于相对较大的肌钙蛋白复合物所致。在僵直条件下用肌球蛋白亚片段-1对细肌丝进行标记似乎不受肌钙蛋白的影响。异步飞行肌的肌钙蛋白缺乏脊椎动物横纹肌的肌钙蛋白I成分。肌钙蛋白H仅存在于飞行肌中,可能参与该肌肉的拉伸激活过程。

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