Calcium-dependent inhibition of in vitro thin-filament motility by native titin

被引:114
作者
Kellermayer, MSZ [1 ]
Granzier, HL [1 ]
机构
[1] WASHINGTON STATE UNIV, DEPT VET COMPARAT ANAT PHARMACOL & PHYSIOL, PULLMAN, WA 99164 USA
关键词
muscle contraction; motility (in vitro); titin; calcium regulation; F-actin; thin filament;
D O I
10.1016/0014-5793(96)00055-5
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Titin (also known as connectin) is a giant filamentous protein that spans the distance between the Z- and NI-lines of the vertebrate muscle sarcomere and plays a fundamental role in the generation of passive tension. Titin has been shown to bind strongly to myosin, making it tightly associated to the thick filament in the sarcomere. Recent observations have suggested the possibility that titin also interacts with actin, implying further functions of titin in muscle contraction, We show - using in vitro motility and binding assays - that native titin interacts with both filamentous actin and reconstituted thin filaments. The interaction results in the inhibition of the filaments' in vitro motility. Furthermore, the thin-thin filament interaction occurs in a calcium-dependent manner: increased calcium results in enhanced binding of thin filaments to titin and greater suppression of in vitro motility.
引用
收藏
页码:281 / 286
页数:6
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