Laboratory for Fluorescence Dynamics, Department of Biomedical Engineering, University of California, Irvine, CA 92697, USA.
Proc Natl Acad Sci U S A. 2010 Sep 21;107(38):16560-5. doi: 10.1073/pnas.1006731107. Epub 2010 Sep 7.
No methods proposed thus far have the capability to measure overall molecular flow in the nucleus of living cells. Here, we apply the pair correlation function analysis (pCF) to measure molecular anisotropic diffusion in the interphase nucleus of live cells. In the pCF method, we cross-correlate fluctuations at several distances and locations within the nucleus, enabling us to define migration paths and barriers to diffusion. We use monomeric EGFP as a prototypical inert molecule and measure flow in and between different nuclear environments. Our results suggest that there are two disconnect molecular flows throughout the nucleus associated with high and low DNA density regions. We show that different density regions of DNA form a networked channel that allows EGFP to diffuse freely throughout, however with restricted ability to traverse the channel. We also observe rare and sudden bursts of molecules traveling across DNA density regions with characteristic time of ≈300 ms, suggesting intrinsic localized change in chromatin structure. This is a unique in vivo demonstration of the intricate chromatin network showing channel directed diffusion of an inert molecule with high spatial and temporal resolution.
迄今为止,尚无方法能够测量活细胞核内的整体分子流。在这里,我们应用对关联函数分析 (pCF) 来测量活细胞间核内分子各向异性扩散。在 pCF 方法中,我们对核内几个距离和位置的波动进行互相关联,从而能够定义迁移路径和扩散障碍。我们使用单体 EGFP 作为典型的惰性分子,并测量在不同核环境中的流动。我们的结果表明,整个核内存在两种不连续的分子流,与高和低 DNA 密度区域相关。我们表明,不同密度的 DNA 区域形成一个网络化的通道,允许 EGFP 自由扩散,但通过通道的能力受到限制。我们还观察到分子在 DNA 密度区域中罕见且突然的爆发性迁移,具有约 300 毫秒的特征时间,表明染色质结构存在内在的局部变化。这是一个独特的活体内证明,表明复杂的染色质网络以高空间和时间分辨率显示惰性分子的通道定向扩散。