Department of Physics, North Carolina State University, Raleigh, NC, USA.
Lab Chip. 2009 Oct 7;9(19):2772-4. doi: 10.1039/b909217j. Epub 2009 Aug 14.
We present a method for the stretching of chromatin molecules in nanofluidic channels width a cross-section of about 80 x 80 nm(2), and hundreds of microns long. The stretching of chromatin to about 12 basepairs/nm enables location-resolved optical investigation of the nucleic material with a resolution of up to 6 kbp. The stretching is based on the equilibrium elongation that polymers experience when they are introduced into nanofluidic channels that are narrower than the Flory coil corresponding to the whole chromatin molecule. We investigate whether the elongation of reconstituted chromatin can be described by the de Gennes model. We compare nanofluidic stretching of bare DNA and chromatin of equal genomic length, and find that chromatin is 2.5 times more compact in its stretched state.
我们提出了一种在纳米流道中拉伸染色质分子的方法,纳米流道的横截面约为 80x80nm(2),长度可达数百微米。将染色质拉伸至约 12 个碱基对/纳米,可以实现分辨率高达 6 kbp 的核酸物质的定位分辨光学研究。这种拉伸是基于聚合物在被引入比整个染色质分子对应的弗洛里卷曲还要窄的纳米流道时所经历的平衡伸长。我们研究了再构成的染色质的伸长是否可以用德根内斯模型来描述。我们比较了裸 DNA 和基因组长度相等的染色质的纳米流道拉伸,发现拉伸状态下的染色质紧凑了 2.5 倍。