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使用共聚焦激光显微镜的扫描浓度相关光谱学。

Scanning concentration correlation spectroscopy using the confocal laser microscope.

作者信息

Koppel D E, Morgan F, Cowan A E, Carson J H

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06030.

出版信息

Biophys J. 1994 Feb;66(2 Pt 1):502-7. doi: 10.1016/s0006-3495(94)80801-x.

Abstract

Concentration correlation spectroscopy allows the assessment of molecular motions in complex systems. The technique generally monitors concentration fluctuations by means of some method such as the intensity of fluorescent molecules (fluorescence correlation spectroscopy). We describe here the use of scanning confocal laser microscopy to measure correlation functions in both space and time. This methodology offers two major advantages over conventional methods. First, collecting data from different regions of the sample significantly increases the signal-to-noise ratio. Second, molecular motions of colloidal gold can be analyzed by correlation methods with high temporal and spatial resolution. Using a MRC 600 laser scanning system, we collect data from an ensemble of 768 independent subvolumes and determine the space-time correlation function. We demonstrate the technique using two different types of samples, fluorescently labeled DNA molecules in solution and colloidal gold-tagged lipids in a planar bilayer. This approach, which we term "scanning concentration correlation spectroscopy," provides a straightforward means of performing high resolution correlation analysis of molecular motions with available instrumentation.

摘要

浓度相关光谱法可用于评估复杂系统中的分子运动。该技术通常通过某些方法(如荧光分子强度,即荧光相关光谱法)来监测浓度波动。我们在此描述了使用扫描共聚焦激光显微镜来测量空间和时间上的相关函数。与传统方法相比,这种方法具有两个主要优点。第一,从样品的不同区域收集数据可显著提高信噪比。第二,胶体金的分子运动可以通过具有高时间和空间分辨率的相关方法进行分析。使用MRC 600激光扫描系统,我们从768个独立子体积的集合中收集数据,并确定时空相关函数。我们使用两种不同类型的样品展示了该技术,即溶液中荧光标记的DNA分子和平面双层中胶体金标记的脂质。我们将这种方法称为“扫描浓度相关光谱法”,它提供了一种使用现有仪器对分子运动进行高分辨率相关分析的直接手段。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca6e/1275716/54acd4f6196b/biophysj00079-0233-a.jpg

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