Department of Molecular Physiology and Biophysics, University of Vermont, Burlington, VT 05405, USA.
Proc Natl Acad Sci U S A. 2011 Aug 23;108(34):E535-41. doi: 10.1073/pnas.1104298108. Epub 2011 Aug 1.
Myosin Va (myoV) and myosin VI (myoVI) are processive molecular motors that transport cargo in opposite directions on actin tracks. Because these motors may bind to the same cargo in vivo, we developed an in vitro "tug of war" to characterize the stepping dynamics of single quantum-dot-labeled myoV and myoVI motors linked to a common cargo. MyoV dominates its myoVI partner 79% of the time. Regardless of which motor wins, its stepping rate slows due to the resistive load of the losing motor (myoV, 2.1 pN; myoVI, 1.4 pN). Interestingly, the losing motor steps backward in synchrony with the winning motor. With ADP present, myoVI acts as an anchor to prevent myoV from stepping forward. This model system emphasizes the physical communication between opposing motors bound to a common cargo and highlights the potential for modulating this interaction by changes in the cell's ionic milieu.
肌球蛋白 Va(myoV)和肌球蛋白 VI(myoVI)是在肌动蛋白轨道上向相反方向运输货物的进行性分子马达。因为这些马达在体内可能与相同的货物结合,所以我们开发了一种体外“拔河”实验来描述与共同货物相连的单个量子点标记的 myoV 和 myoVI 马达的步进动力学。myoV 主导其 myoVI 伙伴 79%的时间。无论哪个马达获胜,由于失去的马达(myoV,2.1 pN;myoVI,1.4 pN)的阻力负载,其步进速度都会减慢。有趣的是,失去的马达与获胜的马达同步向后步进。当存在 ADP 时,myoVI 充当锚点,防止 myoV 向前步进。该模型系统强调了绑定到共同货物的相反马达之间的物理通信,并突出了通过细胞离子环境的变化来调节这种相互作用的潜力。