Thrower D A, Jordan M A, Schaar B T, Yen T J, Wilson L
Department of Biological Sciences, University of California, Santa Barbara 93106.
EMBO J. 1995 Mar 1;14(5):918-26. doi: 10.1002/j.1460-2075.1995.tb07073.x.
A minus end-directed microtubule motor activity from extracts of HeLa cells blocked at prometaphase/metaphase of mitosis with vinblastine has been partially purified and characterized. The motor activity was eliminated by immunodepletion of Centromere binding protein E (CENP-E). The CENP-E-associated motor activity, which was not detectable in interphase cells, moved microtubules at mean rates of 0.46 micron/s at 37 degrees C and 0.24 micron/s at 25 degrees C. The motor activity co-purified with CENP-E through several purification procedures. Motor activity was clearly not due to dynein or to kinesin. The microtubule gliding rates of the CENP-E-associated motor were different from those of dynein and kinesin. In addition, the pattern of nucleotide substrate utilization by the CENP-E-associated motor and the sensitivity to inhibitors were different from those of dynein and kinesin. The CENP-E-associated motor had an apparent native molecular weight of 874,000 Da and estimated dimensions of 2 nm x 80 nm. This is the first demonstration of motor activity associated with CENP-E, strongly supporting the hypothesis that CENP-E may act as a minus end-directed microtubule motor during mitosis.
用长春花碱使处于有丝分裂前中期/中期的HeLa细胞提取物中的一种负端定向微管马达活性得到了部分纯化和表征。通过免疫去除着丝粒结合蛋白E(CENP-E)可消除该马达活性。与CENP-E相关的马达活性在间期细胞中无法检测到,在37℃时以平均0.46微米/秒的速度移动微管,在25℃时以0.24微米/秒的速度移动微管。该马达活性通过几种纯化程序与CENP-E共纯化。马达活性显然不是由动力蛋白或驱动蛋白引起的。与CENP-E相关的马达的微管滑动速度与动力蛋白和驱动蛋白的不同。此外,与CENP-E相关的马达对核苷酸底物的利用模式和对抑制剂的敏感性与动力蛋白和驱动蛋白的不同。与CENP-E相关的马达的表观天然分子量为874,000道尔顿,估计尺寸为2纳米×80纳米。这是首次证明与CENP-E相关的马达活性,有力地支持了CENP-E在有丝分裂期间可能作为负端定向微管马达起作用的假说。