Department of Biochemistry, Groningen Biomolecular Science and Biotechnology Institute, Netherlands Proteomics Centre & Zernike Institute for Advanced Materials, University of Groningen, Nijenborgh 4, Groningen, The Netherlands.
Curr Opin Biotechnol. 2011 Feb;22(1):117-26. doi: 10.1016/j.copbio.2010.09.009. Epub 2010 Oct 16.
We review recent observations on the mobility of macromolecules and their spatial organization in live bacterial cells. We outline the major fluorescence microscopy-based methods to determine the mobility and thus the diffusion coefficients (D) of molecules, which is not trivial in small cells. The extremely high macromolecule crowding of prokaryotes is used to rationalize the reported lower diffusion coefficients as compared to eukaryotes, and we speculate on the nature of the barriers for diffusion observed for proteins (and mRNAs) in vivo. Building on in vitro experiments and modeling studies, we evaluate the size dependence of diffusion coefficients for macromolecules in vivo, in case of both water-soluble and integral membrane proteins. We comment on the possibilities of anomalous diffusion and provide examples where the macromolecule mobility may be limiting biological processes.
我们回顾了关于生物活细胞中大分子的流动性及其空间组织的最新观察结果。我们概述了主要的荧光显微镜方法,用于确定分子的流动性,从而确定扩散系数(D),这在小细胞中并非易事。原核生物中极高的大分子拥挤度被用来解释与真核生物相比报道的较低扩散系数,并推测了在体内观察到的蛋白质(和 mRNAs)扩散障碍的性质。基于体外实验和模型研究,我们评估了生物体内水溶性和整合膜蛋白的扩散系数的大小依赖性。我们评论了异常扩散的可能性,并提供了大分子流动性可能限制生物过程的例子。