Literature DB >> 3663831

Molecular aggregation characterized by high order autocorrelation in fluorescence correlation spectroscopy.

A G Palmer1, N L Thompson.   

Abstract

The use of high order autocorrelation in fluorescence correlation spectroscopy for investigating aggregation in a sample that contains fluorescent molecules is described. Theoretical expressions for the fluorescence fluctuation autocorrelation functions defined by gm,n(tau) = [(delta fm(t + tau)delta fm(t] - (delta Fm(t] (delta Fn(t]]/(F)m+n, where delta F(t) is the fluorescence fluctuation at time t, (F) is the average fluorescence, and m and n are integers less than or equal to 3, are derived. Methods for determining the number densities and relative fluorescence yields of aggregates of different sizes from a series of Gm,n(0) values are outlined. The method is applied to 1,1'-dioctadecyl-3,3,3',3'-tetramethylindocarbocyanine perchlorate suspended in solutions of water and ethyl alcohol. The technique presented may prove useful in detecting and characterizing aggregates of fluorescent-labeled biological molecules such as cell surface receptors.

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Year:  1987        PMID: 3663831      PMCID: PMC1330077          DOI: 10.1016/S0006-3495(87)83213-7

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  38 in total

1.  Motion of myosin fragments during actin-activated ATPase: fluorescence correlation spectroscopy study.

Authors:  J Borejdo
Journal:  Biopolymers       Date:  1979-11       Impact factor: 2.505

2.  Membrane pores: a computer simulation of interacting pores analyzed by g1(tau) and g2(tau) correlation functions.

Authors:  L S Liebovitch; J Fischbarg
Journal:  J Theor Biol       Date:  1986-04-07       Impact factor: 2.691

3.  Dynamics of fluorescence marker concentration as a probe of mobility.

Authors:  D E Koppel; D Axelrod; J Schlessinger; E L Elson; W W Webb
Journal:  Biophys J       Date:  1976-11       Impact factor: 4.033

4.  Determining the kinetics of membrane pores from patch clamp data without measuring the open and closed times.

Authors:  L S Liebovitch; J Fischbarg
Journal:  Biochim Biophys Acta       Date:  1985-02-28

5.  The major histocompatibility complex class I heavy chain as a structural subunit of the human cell membrane insulin receptor: implications for the range of biological functions of histocompatibility antigens.

Authors:  C Due; M Simonsen; L Olsson
Journal:  Proc Natl Acad Sci U S A       Date:  1986-08       Impact factor: 11.205

6.  Fluorescence correlation spectroscopy. II. An experimental realization.

Authors:  D Magde; E L Elson; W W Webb
Journal:  Biopolymers       Date:  1974-01       Impact factor: 2.505

7.  Fluorescence correlation spectroscopy and photobleaching recovery of multiple binding reactions. II. FPR and FCS measurements at low and high DNA concentrations.

Authors:  R D Icenogle; E L Elson
Journal:  Biopolymers       Date:  1983-08       Impact factor: 2.505

8.  The use of fluorescence correlations spectroscopy to probe chromatin in the cell nucleus.

Authors:  S M Sorscher; J C Bartholomew; M P Klein
Journal:  Biochim Biophys Acta       Date:  1980-11-14

9.  Developing concepts in receptor research.

Authors:  P Cuatrecasas
Journal:  Drug Intell Clin Pharm       Date:  1983-05

10.  Scanning fluorescence correlation spectroscopy. II. Application to virus glycoprotein aggregation.

Authors:  N O Petersen; D C Johnson; M J Schlesinger
Journal:  Biophys J       Date:  1986-04       Impact factor: 4.033

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  53 in total

1.  Molecular dynamics in living cells observed by fluorescence correlation spectroscopy with one- and two-photon excitation.

Authors:  P Schwille; U Haupts; S Maiti; W W Webb
Journal:  Biophys J       Date:  1999-10       Impact factor: 4.033

2.  The photon counting histogram in fluorescence fluctuation spectroscopy.

Authors:  Y Chen; J D Müller; P T So; E Gratton
Journal:  Biophys J       Date:  1999-07       Impact factor: 4.033

3.  Resolving heterogeneity on the single molecular level with the photon-counting histogram.

Authors:  J D Müller; Y Chen; E Gratton
Journal:  Biophys J       Date:  2000-01       Impact factor: 4.033

4.  Probing ligand protein binding equilibria with fluorescence fluctuation spectroscopy.

Authors:  Y Chen; J D Müller; S Y Tetin; J D Tyner; E Gratton
Journal:  Biophys J       Date:  2000-08       Impact factor: 4.033

5.  Cellular characterization of adenylate kinase and its isoform: two-photon excitation fluorescence imaging and fluorescence correlation spectroscopy.

Authors:  Qiaoqiao Ruan; Yan Chen; Enrico Gratton; Michael Glaser; William W Mantulin
Journal:  Biophys J       Date:  2002-12       Impact factor: 4.033

6.  Two-photon fluorescence coincidence analysis: rapid measurements of enzyme kinetics.

Authors:  Katrin G Heinze; Markus Rarbach; Michael Jahnz; Petra Schwille
Journal:  Biophys J       Date:  2002-09       Impact factor: 4.033

7.  Fluorescence correlation spectroscopy with high-order and dual-color correlation to probe nonequilibrium steady states.

Authors:  Hong Qian; Elliot L Elson
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-17       Impact factor: 11.205

8.  Global analysis of fluorescence fluctuation data.

Authors:  Victor V Skakun; Mark A Hink; Anatoli V Digris; Ruchira Engel; Eugene G Novikov; Vladimir V Apanasovich; Antonie J W G Visser
Journal:  Eur Biophys J       Date:  2005-02-12       Impact factor: 1.733

9.  Rapid analysis of Forster resonance energy transfer by two-color global fluorescence correlation spectroscopy: trypsin proteinase reaction.

Authors:  Christian Eggeling; Peet Kask; Dirk Winkler; Stefan Jäger
Journal:  Biophys J       Date:  2005-04-22       Impact factor: 4.033

10.  Molecular brightness determined from a generalized form of Mandel's Q-parameter.

Authors:  Alvaro Sanchez-Andres; Yan Chen; Joachim D Müller
Journal:  Biophys J       Date:  2005-09-02       Impact factor: 4.033

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