NEBULIN AS A GIANT ACTIN-BINDING TEMPLATE PROTEIN IN SKELETAL-MUSCLE SARCOMERE - INTERACTION OF ACTIN AND CLONED HUMAN NEBULIN FRAGMENTS

被引:76
作者
JIN, JP [1 ]
WANG, K [1 ]
机构
[1] UNIV TEXAS,DEPT CHEM & BIOCHEM,CLAYTON FDN,INST BIOCHEM,AUSTIN,TX 78712
关键词
NEBULIN; ACTIN-BINDING PROTEIN; MUSCLE THIN FILAMENT; CDNA EXPRESSION IN ESCHERICHIA-COLI; ELISA;
D O I
10.1016/0014-5793(91)80366-B
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 (> 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 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.
引用
收藏
页码:93 / 96
页数:4
相关论文
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