Recognition Imaging of Acetylated Chromatin Using a DNA Aptamer

被引:13
|
作者
Lin, Liyun [1 ,2 ]
Fu, Qiang [1 ,2 ]
Williams, Berea A. R. [1 ,2 ]
Azzaz, Abdelhamid M. [4 ]
Shogren-Knaak, Michael A. [4 ]
Chaput, John C. [1 ,2 ]
Lindsay, Stuart [1 ,2 ,3 ]
机构
[1] Arizona State Univ, Biodesign Inst, Tempe, AZ 85287 USA
[2] Arizona State Univ, Dept Phys, Tempe, AZ 85287 USA
[3] Arizona State Univ, Dept Chem & Biochem, Tempe, AZ 85287 USA
[4] Iowa State Univ, Dept Biochem Biophys & Mol Biol, Ames, IA USA
基金
美国国家卫生研究院;
关键词
IN-VITRO SELECTION; HISTONE; MICROSCOPY; EVOLUTION; RNA; LIGANDS;
D O I
10.1016/j.bpj.2009.06.045
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Histone acetylation plays an important role in the regulation of gene expression. A DNA aptamer generated by in vitro selection to be highly specific for histone H4 protein acetylated at lysine 16 was used as a recognition element for atomic force microscopy-based recognition imaging of synthetic nucleosomal arrays with precisely controlled acetylation. The aptamer proved to be reasonably specific at recognizing acetylated histones, with recognition efficiencies of 60% on-target and 12% off-target. Though this selectivity is much poorer than the >2000:1 equilibrium specificity of the aptamer, it is a large improvement on the performance of a ChIP-quality antibody, which is not selective at all in this application, and it should permit high-fidelity recognition with repeated imaging. The ability to image the precise location of posttranslational modifications may permit nanometer-scale investigation of their effect on chromatin structure.
引用
收藏
页码:1804 / 1807
页数:4
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