Wang Y M, Austin Robert H, Cox Edward C
Department of Physics, Princeton University, Princeton, New Jersey 08544, USA.
Phys Rev Lett. 2006 Jul 28;97(4):048302. doi: 10.1103/PhysRevLett.97.048302. Epub 2006 Jul 27.
We used single-molecule imaging techniques and measured the one-dimensional diffusion of LacI repressor proteins along elongated DNA to address the long-standing puzzle of why some proteins find their targets faster than allowed by 3D diffusion. Our analysis of the LacI transcription factor's diffusion yielded four main results: (1) LacI diffuses along nonspecific sequences of DNA in the form of 1D Brownian motion; (2) the observed 1D diffusion coefficients D1vary over an unexpectedly large range, from 2.3x10(-12) cm2/s to 1.3x10(-9) cm2/s; (3) the lengths of DNA covered by these 1D diffusions vary from 120 nm to 2920 nm; and (4) the mean values of D1 and the diffusional lengths indeed predict a LacI target binding rate 90 times faster than the 3D diffusion limit.
我们运用单分子成像技术,测量了LacI阻遏蛋白沿拉长的DNA的一维扩散,以解决长期存在的谜题:为何有些蛋白质找到其靶标的速度比三维扩散所允许的速度更快。我们对LacI转录因子扩散的分析得出了四个主要结果:(1)LacI以一维布朗运动的形式沿DNA的非特异性序列扩散;(2)观察到的一维扩散系数D1在一个意想不到的大范围内变化,从2.3×10⁻¹²平方厘米/秒到1.3×10⁻⁹平方厘米/秒;(3)这些一维扩散所覆盖的DNA长度从120纳米到2920纳米不等;(4)D1的平均值和扩散长度确实预测LacI靶标结合速率比三维扩散极限快90倍。