Department of Electrical and Computer Engineering , University of Minnesota Twin Cities , Minneapolis , Minnesota 55455 , United States.
Department of Genetics, Cell Biology, and Development , University of Minnesota Twin Cities , Minneapolis , Minnesota 55108 , United States.
Biochemistry. 2019 Nov 26;58(47):4721-4725. doi: 10.1021/acs.biochem.9b00422. Epub 2019 Sep 20.
We examine the effect of cargo-motor linkage stiffness on the mechanobiological properties of the molecular motor myosin VI. We use the programmability of DNA nanostructures to modulate cargo-motor linkage stiffness and combine it with high-precision optical trapping measurements to measure the effect of linkage stiffness on the motile properties of myosin VI. Our results reveal that a stiff cargo-motor linkage leads to shorter step sizes and load-induced anchoring of myosin VI, while a flexible linkage results in longer steps with frequent detachments from the actin filament under load. Our findings suggest a novel regulatory mechanism for tuning the dual cellular roles of the anchor and transporter ascribed to myosin VI.
我们研究了货物-马达连接刚度对分子马达肌球蛋白 VI 的机械生物学特性的影响。我们利用 DNA 纳米结构的可编程性来调节货物-马达连接刚度,并将其与高精度光学捕获测量相结合,以测量连接刚度对肌球蛋白 VI 运动特性的影响。我们的结果表明,刚性货物-马达连接导致肌球蛋白 VI 的步幅变短且负载诱导的固定,而柔性连接则导致在负载下与肌动蛋白丝频繁脱离的更长步幅。我们的发现为调节肌球蛋白 VI 的锚定和运输双重细胞功能提供了一种新的调控机制。