Lockhart A, Cross R A, McKillop D F
Molecular Motors Group, Marie Curie Research Institute, Oxted, Surrey, UK.
FEBS Lett. 1995 Jul 24;368(3):531-5. doi: 10.1016/0014-5793(95)00723-m.
The motor protein non-claret disjunctional (ncd) moves towards the minus ends of microtubules (MTs), whereas its close relative kinesin moves in the opposite direction towards the plus ends of MTs. The mechanisms of movement and directional reversal for these motor proteins are unknown. Here we report the rate constants for MT activated ADP release from a recombinant double-headed ncd protein, GST-MC5, and a recombinant double-headed kinesin protein, K delta 401, measured using the fluorescent nucleotide analogues methylanthranilyol ATP (mantATP) and mantADP. Comparison of the maximal MT activated mantADP release rates for these proteins with their maximal MT activated mantATP turnover rates indicates that ADP release is the rate-limiting step for ATP turnover for both ncd and kinesin. This data supports the view that directional reversal may result from structural rather than chemical kinetic differences in the way the motors interact with MTs.
动力蛋白非红化分离蛋白(ncd)向微管(MTs)的负极移动,而其近亲驱动蛋白则向相反方向,即MTs的正极移动。这些动力蛋白的运动和方向反转机制尚不清楚。在此,我们报告了使用荧光核苷酸类似物甲基邻氨基苯甲酸腺苷三磷酸(mantATP)和甲基邻氨基苯甲酸腺苷二磷酸(mantADP)测量的,微管激活的重组双头ncd蛋白GST-MC5和重组双头驱动蛋白K delta 401释放ADP的速率常数。将这些蛋白的最大微管激活mantADP释放速率与其最大微管激活mantATP周转速率进行比较,结果表明,ADP释放是ncd和驱动蛋白ATP周转的限速步骤。该数据支持这样一种观点,即方向反转可能是由于动力蛋白与微管相互作用方式的结构差异而非化学动力学差异导致的。