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用光镊对单个驱动蛋白分子施加应力。

Single kinesin molecules stressed with optical tweezers.

作者信息

Kuo S C, Ramanathan K, Sorg B

机构信息

Department of Biomedical Engineering, Johns Hopkins University, Baltimore, Maryland 21205, USA.

出版信息

Biophys J. 1995 Apr;68(4 Suppl):74S.

Abstract

Using the optical tweezers to pull on microtubules, we have stretched and twisted single kinesin molecules adsorbed to glass surfaces. Preliminary measurements suggest that the mechanical system is very compliant, with an apparent stretch of 120 nm with < 2 pN of force. Although measurements of the series compliance of the bead-microtubule structure are still in progress, the kinesin attachment site does not slip with stretch. However, under torsional stress, kinesin appears to slip. With torques < 2 pN-microns approximately 1 Hz in 2 mM AMP-PNP, there is no apparent limit to the number of revolutions that the microtubule can rotate around the kinesin attachment site (n = 44). Preliminary data from other nucleotide conditions are similar. Although there are rare instances of torsional elasticity where the attachment site unwinds, the restoring forces are not constant with angular position, also indicating slippage. Mechanisms of mechanochemical transduction must account for linear force generation in the presence of angular "slippage."

摘要

利用光镊牵拉微管,我们拉伸并扭转了吸附在玻璃表面的单个驱动蛋白分子。初步测量表明,该机械系统具有很高的柔韧性,在小于2皮牛的力作用下,明显拉伸可达120纳米。尽管对珠子-微管结构的串联柔韧性测量仍在进行中,但驱动蛋白附着位点在拉伸时不会滑动。然而,在扭转应力下,驱动蛋白似乎会滑动。在2毫摩尔腺苷-5'-三磷酸γ-亚氨酰基二磷酸(AMP-PNP)中,当扭矩小于2皮牛-微米且频率约为1赫兹时,微管围绕驱动蛋白附着位点旋转的圈数似乎没有明显限制(n = 44)。来自其他核苷酸条件的初步数据也类似。尽管存在罕见的扭转弹性情况,即附着位点会解旋,但恢复力并不随角位置恒定,这也表明存在滑动。机械化学转导机制必须解释在存在角“滑动”的情况下如何产生线性力。

相似文献

9
The mechanics of force generation by kinesin.驱动蛋白产生力的机制。
Biophys J. 1995 Apr;68(4 Suppl):245S-253S; 253S-255S.

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