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Electrophoretic control of actomyosin motility

机译:肌动球蛋白运动的电泳控制

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The effect of DC electric field strength on in vitro actomyosin motility was examined. Rabbit skeletal muscle heavymeromyosin (HMM) was adsorbed to nitrocellulose-coated glass, and the myosin driven movement of fluorescentlylabeled actin filaments was recorded in the presence of 0 to 9000 V m-1 applied DC voltage. The applied electric fieldresulted in increased filament velocity and oriented actin movement, with leading heads of filaments directed towardsthe positive electrode. Velocity (v) was found to increase moderately with electric field strength at applied fields up to~ 4500 V m~(-1) (Δv/ΔE = 0.037 μm~2 V~(-1)sec~(-1)), and then increased at a more rapid rate (Δv/ΔE = 0.100 μm~2 V-1sec~(-1)) athigher field strengths up to 9000 V m-1. The electrophoretic effect caused up to 70% of actin motion to be orientedwithin 30 degrees of the positive electrode, with the largest effect observed using an applied field of 6000 V m~(-1).Higher electric field strengths caused filament breakage.
机译:检查了直流电场强度对体外肌动球蛋白运动性的影响。将兔骨骼肌重肌球蛋白(HMM)吸附到涂有硝酸纤维素的玻璃上,并在施加0至9000 V m-1的直流电压的情况下记录肌球蛋白驱动的荧光标记肌动蛋白丝的运动。施加的电场导致灯丝速度增加和定向的肌动蛋白运动,灯丝的前导头指向正极。发现在施加电场至约4500 V m〜(-1)(Δv/ΔE= 0.037μm〜2 V〜(-1)sec〜(-1))时,速度(v)随电场强度而适度增加,然后在高达9000 V m-1的更高场强下以更快的速率增加(Δv/ΔE= 0.100μm〜2 V-1sec〜(-1))。电泳效应导致多达70%的肌动蛋白运动在正极的30度范围内取向,在施加6000 V m〜(-1)的电场时观察到的效应最大。较高的电场强度导致灯丝断裂。

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    Industrial Research Institute Swinburne Faculty of Engineering and Industrial Science Swinburne University of Technology PO Box 218 Hawthorn VIC 3122 Australia khanson@swin.edu.au phone 61-3-9214-4345 fax 61-3-9214-5050;

    Industrial Research Institute Swinburne Faculty of Engineering and Industrial Science Swinburne mUniversity of Technology PO Box 218 Hawthorn VIC 3122 Australia;

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