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伴肌动蛋白作为骨骼肌肌节中的一种巨大的肌动蛋白结合模板蛋白。肌动蛋白与克隆的人伴肌动蛋白片段的相互作用。

Nebulin as a giant actin-binding template protein in skeletal muscle sarcomere. Interaction of actin and cloned human nebulin fragments.

作者信息

Jin J P, Wang K

机构信息

Department of Chemistry and Biochemistry, University of Texas, Austin 78712.

出版信息

FEBS Lett. 1991 Apr 9;281(1-2):93-6. doi: 10.1016/0014-5793(91)80366-b.

Abstract

Nebulin is a family of giant sarcomere matrix proteins of 600-900 kDa in most vertebrate skeletal muscles. Recent sequence analysis suggests that human nebulin is mainly composed of a large number (greater than 200) of conserved repeats of approximately 35 residues. Two cloned nebulin fragments, consisting of 6 and 8 of the repeats, have been expressed in E. coli using the pET3d vector. Both F-actin cosedimentation and solid-phase binding assays demonstrated a specific binding of these nebulin fragments to actin. This finding suggests that nebulin is a giant protein which binds actin at multiple sites in a template-manner. The presence of an actin-binding template protein in the skeletal muscle sarcomere may have significant implications in the assembly and function of the contractile apparatus.

摘要

伴肌动蛋白是大多数脊椎动物骨骼肌中600 - 900 kDa的巨肌节基质蛋白家族。最近的序列分析表明,人伴肌动蛋白主要由大约35个残基的大量(超过200个)保守重复序列组成。两个由6个和8个重复序列组成的克隆伴肌动蛋白片段,已使用pET3d载体在大肠杆菌中表达。F - 肌动蛋白共沉降和固相结合试验均证明这些伴肌动蛋白片段与肌动蛋白有特异性结合。这一发现表明伴肌动蛋白是一种以模板方式在多个位点结合肌动蛋白的巨大蛋白质。骨骼肌肌节中肌动蛋白结合模板蛋白的存在可能对收缩装置的组装和功能具有重要意义。

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