Lighting Up Individual DNA Binding Proteins with Quantum Dots

被引:39
作者
Ebenstein, Yuval [1 ,2 ]
Gassman, Natalie [1 ]
Kim, Soohong [1 ]
Antelman, Josh [1 ]
Kim, Younggyu [1 ]
Ho, Sam [1 ]
Samuel, Robin [1 ]
Michalet, Xavier [1 ]
Weiss, Shimon [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Dept Chem & Biochem, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, DOE Inst Genom & Prote, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Geffen Med Sch, Dept Physiol, Los Angeles, CA 90095 USA
关键词
TRANSCRIPTION; BACTERIOPHAGE-T7; COLOCALIZATION; MICROSCOPY; PROMOTER; SEQUENCE; SYSTEM;
D O I
10.1021/nl803820b
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The ability to determine the precise loci and occupancy of DNA-binding proteins is instrumental to our understanding of cellular processes like gene expression and regulation. We propose a single-molecule approach for the direct visualization of proteins bound to their template DNA. Fluorescent quantum dots (QD) are used to label proteins bound to DNA, allowing multicolor, nanometer-resolution localization. Protein-DNA complexes are linearly extended and imaged to determine the precise location of the protein binding sites. The method is demonstrated by detecting individual OD-labeled T7-RNA polymerases on the T7 bacteriophage genome. This work demonstrates the potential of this approach to precisely read protein binding position or, alternatively, "write" such information on extended DNA with ODs via sequence-specific molecular recognition.
引用
收藏
页码:1598 / 1603
页数:6
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