Ajtai K, Pótó L, Burghardt T P
Department of Biochemistry and Molecular Biology, Mayo Foundation, Rochester, Minnesota 55905.
Biochemistry. 1990 Aug 21;29(33):7733-41. doi: 10.1021/bi00485a023.
The nitroxide spin label (iodoacetamido)proxyl (IPSL) was specifically and rigidly attached to sulfhydryl 1 (SH1) on myosin subfragment 1 (S1). The specificity of this label for SH1 was demonstrated by using a technique where the spin label is localized on the electrophoresis-isolated proteolytic fragments of myosin using electron paramagnetic resonance (EPR). Studies of the rigidity of the probe on SH1 indicate that the IPSL is immobilized on the surface of S1 in the presence and absence of the nucleotides MgADP or MgATP. The EPR spectrum of muscle fibers decorated with IPSL-S1 shows that the IPSL-S1 rotates from its orientation in rigor upon binding MgADP. The angular displacement due to nucleotide binding is larger than that detected with the (maleimido)tempo spin label [Ajtai, K., French, A. R., & Burghardt, T. P. (1989) Biophys. J. 56, 535-541], demonstrating that the IPSL is oriented on the myosin cross-bridge in a manner that is favorable for detecting cross-bridge rotation during the rigor to MgADP state transition.
氮氧自由基自旋标记物(碘乙酰胺基)脯氨酰自由基(IPSL)被特异性且牢固地连接到肌球蛋白亚片段1(S1)上的巯基1(SH1)。通过一种利用电子顺磁共振(EPR)将自旋标记物定位在肌球蛋白电泳分离的蛋白水解片段上的技术,证明了该标记物对SH1的特异性。对SH1上探针刚性的研究表明,在存在和不存在核苷酸MgADP或MgATP的情况下,IPSL都固定在S1的表面。用IPSL-S1装饰的肌肉纤维的EPR光谱表明,IPSL-S1在结合MgADP时从其在僵直状态下的方向旋转。由于核苷酸结合引起的角位移大于用(马来酰亚胺)Tempo自旋标记物检测到的角位移[Ajtai, K., French, A. R., & Burghardt, T. P. (1989) Biophys. J. 56, 535 - 541],这表明IPSL以有利于检测从僵直状态到MgADP状态转变过程中横桥旋转的方式定向在肌球蛋白横桥上。