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应用荧光共振能量转移(FRET)显微镜研究 DNA 自组装单层(SAMs)在金电极上的局部环境和动力学。

Application of FRET Microscopy to the Study of the Local Environment and Dynamics of DNA SAMs on Au Electrodes.

机构信息

Chimie Analytique et Chimie des Interfaces, Faculté des Sciences , Université Libre de Bruxelles (ULB) , Bruxelles 1050 , Belgium.

出版信息

Langmuir. 2018 Dec 11;34(49):14802-14810. doi: 10.1021/acs.langmuir.8b02131. Epub 2018 Sep 20.

Abstract

Immobilized DNA probe strands self-assembled on an electrode surface are the bases of many electrochemically based biosensors. Control or measurement of the local environment around each DNA molecule tethered to the electrode surface is needed because the local environment can influence the binding or hybridization efficiency of the target in solution. Measurement of this local environment in buffer or under electrochemical control can be challenging. Here we demonstrate the use of fluorescence microscopy and a Förster resonance energy transfer (FRET) methodology to characterize multicomponent DNA SAMs. The DNA SAMs that were studied were composed of a series of mole fraction ratios of alkylthiol-modified DNA which was labeled with either AlexaFluor488 or AlexaFluor647, a FRET donor and acceptor, respectively. The DNA SAMs were hybridized before assembly onto the electrode surface. Wide-field filter-based FRET microscopy was used to study the assembly of DNA SAMs onto gold bead electrodes. These single-crystal gold bead electrodes contain many surface crystallographic regions which enable the comparison of the adsorbed DNA local environment. These surfaces show that most surface modifications are uniformly prepared, and the FRET efficiency can be explained through simple surface density considerations. The FRET efficiency for different compositions of the donor and acceptor for these regions is also explained through 2D FRET modeling. Not all surfaces were similar to the (111) and (110) regions showing deviations from the expected FRET behavior. Also demonstrated is FRET imaging using a confocal microscope. This approach proves useful in the analysis of a more dynamic system, such as the analysis of reductive desorption of the mixed-component DNA SAM. FRET microscopy is useful for surface analysis of the DNA local environment, enabling a measure of the surface modification, local density, and clustering and eventually a new detection modality.

摘要

固定在电极表面上的 DNA 探针链自组装是许多基于电化学的生物传感器的基础。需要控制或测量与电极表面连接的每个 DNA 分子周围的局部环境,因为局部环境会影响溶液中靶标的结合或杂交效率。在缓冲液中或在电化学控制下测量这种局部环境可能具有挑战性。在这里,我们展示了使用荧光显微镜和Förster 共振能量转移(FRET)方法来表征多组分 DNA SAM。所研究的 DNA SAM 由一系列烷基硫醇修饰的 DNA 的摩尔分数比组成,这些 DNA 分别用 AlexaFluor488 或 AlexaFluor647 标记,分别为 FRET 供体和受体。在将 SAM 组装到电极表面之前,将 DNA SAM 进行杂交。使用基于宽场滤光片的 FRET 显微镜研究 DNA SAM 组装到金珠电极上。这些单晶金珠电极包含许多表面结晶区域,使我们能够比较吸附 DNA 的局部环境。这些表面表明,大多数表面修饰都是均匀制备的,并且可以通过简单的表面密度考虑来解释 FRET 效率。还通过二维 FRET 建模解释了这些区域的供体和受体的不同组成的 FRET 效率。并非所有表面都与(111)和(110)区域相似,显示出与预期 FRET 行为的偏差。还展示了使用共焦显微镜进行 FRET 成像。这种方法在分析更动态的系统时非常有用,例如混合组分 DNA SAM 的还原解吸分析。FRET 显微镜可用于分析 DNA 局部环境的表面,可用于测量表面修饰、局部密度、聚集程度,并最终实现新的检测模式。

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