首页> 外文会议>2011 International Workshop on Biophotonics >Combined optical trapping and nanometer-precision localization for the single-molecule study of DNA-binding proteins
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Combined optical trapping and nanometer-precision localization for the single-molecule study of DNA-binding proteins

机译:结合光阱和纳米精度定位技术进行DNA结合蛋白的单分子研究

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The development of an increasing variety of single-molecule techniques has provided remarkable insights on several biological processes. Recently, tremendous improvements have been achieved in the precision of localization of single fluorescent molecules, allowing localization and tracking of biomolecules at the nm level. In the present work, we describe a single-molecule assay, based on the combination of two different single-molecule techniques in the same experimental setup: nanometer-precision Fluorescence Imaging and optical Trapping (FIAT). A microfluidic chamber allows fast exchange of the sample buffer between two different buffer compositions. The main advantage of the FIAT assay is the possibility of detecting the position of a single fluorescently labeled biomolecule and characterize its dynamics of interaction with the substrate, while precisely controlling the mechanical properties of the substrate itself. These features make FIAT well suitable for the study of several biological systems, including DNA-binding proteins and molecular motors. Here, we present preliminary results obtained with two proteins: RNA polymerase (RNAp) and the lactose repressor (LacI): two crucial proteins involved in prokaryotic gene expression and its regulation. RNAp, in a stalled ternary complex, was labeled with a quantum dot and localized on the T7 promoter. The DNA molecule containing the promoter was suspended between two optical traps and the position of RNAp was measured with a precision of ∼ 4 nm. For the study of LacI, the protein is labeled with a quantum dot through a genetically-encoded biotin tag at the C-terminal (after the tetramerization domain) and a DNA construct containing two primary operators (O1) is suspended between the two traps. The positions at which binding of LacI takes place are measured. These methods will be extended to the study of dynamics of RNAp and LacI in different mechanical conditions.
机译:越来越多的单分子技术的发展为几种生物学过程提供了非凡的见解。最近,在单个荧光分子的定位精度上已取得了巨大的进步,从而可以在纳米水平上定位和跟踪生物分子。在当前的工作中,我们将基于两种不同的单分子技术在同一实验装置中的组合描述一种单分子测定法:纳米精度荧光成像和光学诱捕(FIAT)。微流体室允许在两种不同的缓冲液组合物之间快速交换样品缓冲液。 FIAT分析的主要优点是可以检测单个荧光标记的生物分子的位置并表征其与底物相互作用的动力学,同时精确控制底物本身的机械性能。这些特征使FIAT非常适合研究几种生物系统,包括DNA结合蛋白和分子马达。在这里,我们介绍用两种蛋白质获得的初步结果:RNA聚合酶(RNAp)和乳糖阻遏物(LacI):参与原核基因表达及其调控的两个关键蛋白质。停滞的三元复合物中的RNAp用量子点标记,并位于T7启动子上。将含有启动子的DNA分子悬浮在两个光阱之间,以约4 nm的精度测量RNAp的位置。对于LacI的研究,该蛋白在C端(四聚体作用域之后)通过遗传编码的生物素标签用量子点标记,并且将包含两个主要操纵子(O1)的DNA构建体悬浮在两个阱之间。测量发生LacI结合的位置。这些方法将扩展到研究不同机械条件下RNAp和LacI的动力学。

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