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通过双色荧光相关光谱分析双分子反应动力学与扩散:利用共振能量转移提高动力学分辨率

Analysis of coupled bimolecular reaction kinetics and diffusion by two-color fluorescence correlation spectroscopy: enhanced resolution of kinetics by resonance energy transfer.

作者信息

Hom Erik F Y, Verkman A S

机构信息

The Graduate Group in Biophysics, Department of Medicine, Cardiovascular Research Institute, University of California, San Francisco, California 94143-0521, USA.

出版信息

Biophys J. 2002 Jul;83(1):533-46. doi: 10.1016/S0006-3495(02)75189-8.

Abstract

In two-color fluorescence correlation spectroscopy (TCFCS), the fluorescence intensities of two fluorescently-labeled species are cross-correlated over time and can be used to identify static and dynamic interactions. Generally, fluorophore labels are chosen that do not undergo Förster resonance energy transfer (FRET). Here, a general TCFCS theory is presented that accounts for the possibility of FRET between reactants in the reversible bimolecular reaction, [reaction: see text] where k(f) and k(b) are forward and reverse rate constants, respectively (dissociation constant K(d) = k(b)/k(f)). Using this theory, we systematically investigated the influence on the correlation function of FRET, reaction rates, reactant concentrations, diffusion, and component visibility. For reactants of comparable size and an energy-transfer efficiency of approximately 90%, experimentally measurable cross-correlation functions should be sensitive to reaction kinetics for K(d) > 10(-8) M and k(f) >or= approximately 10(7) M(-1)s(-1). Measured auto-correlation functions corresponding to donor and acceptor labels are generally less sensitive to reaction kinetics, although for the acceptor, this sensitivity increases as the visibility of the donor increases relative to the acceptor. In the absence of FRET or a significant hydrodynamic difference between reactant species, there is little effect of reaction kinetics on the shape of auto- and cross-correlation functions. Our results suggest that a subset of biologically relevant association-dissociation kinetics can be measured by TCFCS and that FRET can be advantageous in enhancing these effects.

摘要

在双色荧光相关光谱法(TCFCS)中,两种荧光标记物种的荧光强度随时间进行交叉关联,可用于识别静态和动态相互作用。通常,会选择不发生福斯特共振能量转移(FRET)的荧光团标记。在此,我们提出了一种通用的TCFCS理论,该理论考虑了可逆双分子反应中反应物之间发生FRET的可能性,[反应:见正文]其中k(f)和k(b)分别为正向和反向速率常数(解离常数K(d)=k(b)/k(f))。利用该理论,我们系统地研究了FRET、反应速率、反应物浓度、扩散和组分可见性对相关函数的影响。对于尺寸相当且能量转移效率约为90%的反应物,当K(d)>10^(-8) M且k(f)≥约10^(7) M^(-1)s^(-1)时,实验可测量的交叉相关函数应能对反应动力学敏感。对应于供体和受体标记的测量自相关函数通常对反应动力学不太敏感,不过对于受体而言,随着供体相对于受体的可见性增加,这种敏感性会增强。在不存在FRET或反应物物种之间不存在显著流体动力学差异的情况下,反应动力学对自相关和交叉相关函数的形状几乎没有影响。我们的结果表明,TCFCS可以测量一部分生物学相关的缔合 - 解离动力学,并且FRET在增强这些效应方面可能具有优势。

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本文引用的文献

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3
The standard deviation in fluorescence correlation spectroscopy.
Biophys J. 2001 Jun;80(6):2987-99. doi: 10.1016/S0006-3495(01)76264-9.
4
Subcellular targeting by membrane lipids.
Curr Opin Cell Biol. 2001 Apr;13(2):146-52. doi: 10.1016/s0955-0674(00)00191-5.
6
Molecular spectroscopy and dynamics of intrinsically fluorescent proteins: coral red (dsRed) and yellow (Citrine).
Proc Natl Acad Sci U S A. 2000 Oct 24;97(22):11996-2001. doi: 10.1073/pnas.97.22.11996.
7
Simultaneous two-photon excitation of distinct labels for dual-color fluorescence crosscorrelation analysis.
Proc Natl Acad Sci U S A. 2000 Sep 12;97(19):10377-82. doi: 10.1073/pnas.180317197.
9
Probing ligand protein binding equilibria with fluorescence fluctuation spectroscopy.
Biophys J. 2000 Aug;79(2):1074-84. doi: 10.1016/S0006-3495(00)76361-2.
10
Fluorescence correlation spectroscopy: molecular recognition at the single molecule level.
J Mol Recognit. 2000 Mar-Apr;13(2):93-100. doi: 10.1002/(SICI)1099-1352(200003/04)13:2<93::AID-JMR492>3.0.CO;2-6.

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