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肌球蛋白中的发光共振能量转移测量

Luminescence resonance energy transfer measurements in myosin.

作者信息

Burmeister Getz E, Cooke R, Selvin P R

机构信息

Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, USA.

出版信息

Biophys J. 1998 May;74(5):2451-8. doi: 10.1016/s0006-3495(98)77953-6.

Abstract

Myosin is thought to generate force by a rotation between the relative orientations of two domains. Direct measurements of distances between the domains could potentially confirm and quantify these conformational changes, but efforts have been hampered by the large distances involved. Here we show that luminescence resonance energy transfer (LRET), which uses a luminescent lanthanide as the energy-transfer donor, is capable of measuring these long distances. Specifically, we measure distances between the catalytic domain (Cys707) and regulatory light chain domain (Cys108) of the myosin head. An energy transfer efficiency of 21.2 +/- 1.9% is measured in the myosin complex without nucleotide or actin, corresponding to a distance of 73 A, consistent with the crystal structure of Rayment et al. Upon binding to actin, the energy transfer efficiency decreases by 4.5 +/- 1.0%, indicating a conformational change in myosin that involves a relative rotation and/or translation of Cys707 relative to the light chain domain. Addition of ADP also alters the energy transfer efficiency, likely through a rotation of the probe attached to Cys707. These results demonstrate that LRET is capable of making accurate measurements on the relatively large actomyosin complex, and is capable of detecting conformational changes between the catalytic and light chain domains of myosin.

摘要

肌球蛋白被认为是通过两个结构域相对取向之间的旋转来产生力的。对这些结构域之间距离的直接测量有可能证实并量化这些构象变化,但由于涉及的距离较大,相关研究受到了阻碍。在这里,我们表明,以发光镧系元素作为能量转移供体的发光共振能量转移(LRET)能够测量这些长距离。具体而言,我们测量了肌球蛋白头部催化结构域(Cys707)和调节轻链结构域(Cys108)之间的距离。在没有核苷酸或肌动蛋白的肌球蛋白复合物中测得的能量转移效率为21.2±1.9%,对应距离为73 Å,这与Rayment等人的晶体结构一致。与肌动蛋白结合后,能量转移效率降低了4.5±1.0%,表明肌球蛋白发生了构象变化,涉及Cys707相对于轻链结构域的相对旋转和/或平移。添加ADP也会改变能量转移效率,可能是通过连接到Cys707的探针的旋转。这些结果表明,LRET能够对相对较大的肌动球蛋白复合物进行精确测量,并且能够检测肌球蛋白催化结构域和轻链结构域之间的构象变化。

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