Levine B A, Moir A J, Patchell V B, Perry S V
Department of Physiology, University of Birmingham, UK.
FEBS Lett. 1990 Apr 9;263(1):159-62. doi: 10.1016/0014-5793(90)80728-2.
Proton NMR spectroscopy of synthetic peptides corresponding to defined regions of human dystrophin has been employed to study the interaction with F-actin. No evidence of interaction with a C-terminal region corresponding to amino acid residues 3429-3440 was obtained. F-actin restricted the mobility of residues 19-27 in a synthetic peptide corresponding to residues 10-32. This suggests that this is a site of F-actin interaction in the intact dystrophin molecule. Identical sequences to that of residues 19-22 in dystrophin, namely Lys-Thr-Phe-Thr are also present in the N-terminal regions of the alpha-actinins implying this is also a site of F-actin interaction with alpha-actinin.
已采用对应于人类肌营养不良蛋白特定区域的合成肽的质子核磁共振光谱来研究其与F-肌动蛋白的相互作用。未获得与对应于氨基酸残基3429 - 3440的C端区域相互作用的证据。F-肌动蛋白限制了对应于残基10 - 32的合成肽中残基19 - 27的流动性。这表明这是完整肌营养不良蛋白分子中F-肌动蛋白相互作用的位点。肌营养不良蛋白中与残基19 - 22相同的序列,即赖氨酸-苏氨酸-苯丙氨酸-苏氨酸,也存在于α-辅肌动蛋白的N端区域,这意味着这也是F-肌动蛋白与α-辅肌动蛋白相互作用的位点。