IDENTIFICATION AND LOCALIZATION OF HIGH-MOLECULAR-WEIGHT PROTEINS IN INSECT FLIGHT AND LEG MUSCLE

被引:103
|
作者
LAKEY, A
FERGUSON, C
LABEIT, S
REEDY, M
LARKINS, A
BUTCHER, G
LEONARD, K
BULLARD, B
机构
[1] AFRC, INST ANIM PHYSIOL & GENET RES, CAMBRIDGE CB2 4AT, ENGLAND
[2] DUKE UNIV, MED CTR, DEPT CELL BIOL, DURHAM, NC 27710 USA
来源
EMBO JOURNAL | 1990年 / 9卷 / 11期
关键词
connecting filaments; high M(r) proteins; insect muscle; M-line; Z-disc;
D O I
10.1002/j.1460-2075.1990.tb07554.x
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
Thick and thin filaments in asynchronous flight muscle overlap nearly completely and thick filaments are attached to the Z-disc by connecting filaments. We have raised antibodies against a fraction of Lethocerus flight muscle myofibrils containing Z-discs and associated filaments and also against a low ionic strength extract of myofibrils. Monoclonal antibodies were obtained to proteins of 800 kd (p800), 700 kd (p700), 400 kd (p400) and α-actinin. The positions of the proteins in Lethocerus flight and leg myofibrils were determined by immunofluorescence and electron microscopy. p800 is in connecting filaments of flight myofibrils and in A-bands of leg myofibrils. p700 is in Z-discs of flight myofibrils and an immunologically related protein, p500, is in leg muscle Z-discs. p400 is in M-lines of both flight and leg myofibrils. Preliminary DNA sequencing shows that p800 is related to vertebrate titin and nematode twitchin. Molecule of p800 could extend from the Z-disc a short way along thick filaments, forming a mechanical link between the two structures. All three high molecular weight proteins probably stabilize the structure of the myofibril.
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页码:3459 / 3467
页数:9
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