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Atomic force microscopy study of the rabbit skeletal muscle ryanodine receptors in different functional states 被引量:1

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摘要 Atomic force microscope was applied to investigate the effect of extrinsic phospholipid on the structure of rabbit skeletal muscle ryanodine receptor/calcium release channel (RyR1). In addition, in the presence of extrinsic phospholipid, the height and elasticity of the RyR1s in different functional states were also measured. The results indicate: (i) most of the RyR1s showed a normal structure only in the presence of extrinsic phospholipid; (ii) treatment of the RyR1s with AMP and Ca2+ together could increase their Young's Modulus but not change their apparent height; (iii) no detectable change in either height or Young's Modulus of the RyR1s appeared, if the RyR1s were treated with other activators or inhibitors. Atomic force microscope was applied to investigate the effect of extrinsic phospholipid on the structure of rabbit skeletal muscle ryanodine receptor/calcium release channel (RyR1). In addition, in the presence of extrinsic phospholipid, the height and elasticity of the RyR1s in different functional states were also measured. The results indicate: (i) most of the RyR1s showed a normal structure only in the presence of extrinsic phospholipid; (ii) treatment of the RyR1s with AMP and Ca2+ together could increase their Young's Modulus but not change their apparent height; (iii) no detectable change in either height or Young's Modulus of the RyR1s appeared, if the RyR1s were treated with other activators or inhibitors.
出处 《Science China(Life Sciences)》 SCIE CAS 2002年第3期225-236,共12页 中国科学(生命科学英文版)
基金 This work was supported by the Ninth Five-Year Major Research Programs of Chinese Academy of Sciences and the Major National Basic Research Program.
关键词 RYANODINE receptor/calcium release channel ATOMIC force microscope elasticity. ryanodine receptor/calcium release channel, atomic force microscope, elasticity.
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  • 1F. Anthony Lai,Gerhard Meissner. The muscle ryanodine receptor and its intrinsic Ca2+ channel activity[J] 1989,Journal of Bioenergetics and Biomembranes(2):227~246

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