Ordered Arrays of Native Chromatin Molecules for High-Resolution Imaging and Analysis

被引:28
作者
Cerf, Aline [1 ]
Tian, Harvey C. [1 ]
Craighead, Harold G. [1 ]
机构
[1] Cornell Univ, Sch Appl & Engn Phys, Ithaca, NY 14853 USA
基金
美国国家卫生研究院;
关键词
mammalian chromatin; single molecule; soft lithography; molecular stretching; fluorescence imaging; AFM; IN-SITU HYBRIDIZATION; STRETCHED DNA; CENTROMERIC CHROMATIN; SINGLE-MOLECULE; INDIVIDUAL NUCLEOSOMES; DYNAMICS; POLYMER; FIBERS; ORGANIZATION; MICROSCOPY;
D O I
10.1021/nn3023624
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Individual chromatin molecules contain valuable genetic and epigenetic information. To date, there have not been reliable techniques available for the controlled stretching and manipulation of individual chromatin fragments for high-resolution imaging and analysis of these molecules. We report the controlled stretching of single chromatin fragments extracted from two different cancerous cell types (M091 and HeLa) characterized through fluorescence microscopy and atomic force microscopy (AFM). Our method combines soft lithography with molecular stretching to form ordered arrays of more than 250 000 individual chromatin fragments immobilized into a beads-on-a-string structure on a solid transparent support. Using fluorescence microscopy and AFM, we verified the presence of histone proteins after the stretching and transfer process.
引用
收藏
页码:7928 / 7934
页数:7
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