Apocalmodulin and Ca2+ calmodulin bind to the same region on the skeletal muscle Ca2+ release channel

被引:124
作者
Moore, CP
Rodney, G
Zhang, JZ
Santacruz-Toloza, L
Strasburg, G
Hamilton, SL
机构
[1] Baylor Coll Med, Dept Mol Physiol & Biophys, Houston, TX 77030 USA
[2] Michigan State Univ, Dept Food Sci & Human Nutr, E Lansing, MI 48824 USA
关键词
D O I
10.1021/bi9907431
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
The skeletal muscle Ca2+ release channel (RYR1) is regulated by calmodulin in both its Ca2+-free (apocalmodulin) and Ca2+-bound (Ca2+ calmodulin) states. Apocalmodulin is an activator of the channel, and Ca2+ calmodulin is an inhibitor of the channel. Both apocalmodulin and Ca2+ calmodulin binding sites on RYR1 are destroyed by a mild tryptic digestion of the sarcoplasmic reticulum membranes, but calmodulin (either form), bound to RYR1 prior to tryptic digestion, protects both the apocalmodulin and Ca2+ calmodulin sites from tryptic destruction. The protected sites ars after arginines 3630 and 3637 on RYR1. These studies suggest that both Ca2+ calmodulin and apocalmodulin bind to the same or overlapping regions on RYR1 and block access of trypsin to sites at amino acids 3630 and 3637. This sequence is part of a predicted Ca2+ CaM binding site of amino acids 3614-3632 [Takeshima, W., et al, (1989) Nature 339, 439-445].
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页码:8532 / 8537
页数:6
相关论文
共 35 条
  • [1] ALEXANDER KA, 1987, J BIOL CHEM, V262, P6108
  • [2] Ausubel FM., 1998, CURRENT PROTOCOLS MO
  • [3] LABELING OF PROTEINS TO HIGH SPECIFIC RADIOACTIVITIES BY CONJUGATION TO A I-125-CONTAINING ACYLATING AGENT - APPLICATION TO RADIOIMMUNOASSAY
    BOLTON, AE
    HUNTER, WM
    [J]. BIOCHEMICAL JOURNAL, 1973, 133 (03) : 529 - 538
  • [4] BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
  • [5] CALCIUM-DEPENDENT ACTIVATION OF SKELETAL-MUSCLE CA2+ RELEASE CHANNEL (RYANODINE RECEPTOR) BY CALMODULIN
    BURATTI, R
    PRESTIPINO, G
    MENEGAZZI, P
    TREVES, S
    ZORZATO, F
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1995, 213 (03) : 1082 - 1090
  • [6] CALLAWAY C, 1994, J BIOL CHEM, V269, P15876
  • [7] CHANG JZ, 1999, AM J PHYSIOL, V276, pC46
  • [8] CHEN SRW, 1994, J BIOL CHEM, V269, P22698
  • [9] CHIN D, 1989, J BIOL CHEM, V264, P15367
  • [10] FABIATO A, 1988, METHOD ENZYMOL, V157, P378