Literature DB >> 32621863

Fluorescence Correlation Spectroscopy and Photon Counting Histograms in Finite, Bounded Domains.

Yanfei Jiang1, Bingxian Xu2, Artem Melnykov3, Guy M Genin4, Elliot L Elson5.   

Abstract

Analysis of fluctuations arising as fluorescent particles pass through a focused laser beam has enabled quantitative characterization of a broad range of molecular kinetic processes. Two key mathematical frameworks that have enabled these quantifications are fluorescence correlation spectroscopy (FCS) and photon counting histogram (PCH) analysis. Although these frameworks are effective and accurate when the focused laser beam is well approximated by an infinite Gaussian beam with a waist that is small compared to the size of the region over which the fluorescent particles can diffuse, they cannot be applied to situations in which this region is bounded at the nanoscale. We therefore derived general forms of the FCS and PCH frameworks for bounded systems. The finite-domain form of FCS differs from the classical form in its boundary and initial conditions and requires development of a new Fourier space solution for fitting data. Our finite-domain FCS predicts simulated data accurately and reduces to a previous model for the special case when the system is much larger than the Gaussian beam and can be considered to be infinite. We also derived the PCH form for the bounded systems. Our approach enables estimation of the concentration of diffusing fluorophores within a finite domain for the first time, to our knowledge. The method opens the possibility of quantification of kinetics in several systems for which this has never been possible.
Copyright © 2020 Biophysical Society. Published by Elsevier Inc. All rights reserved.

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Year:  2020        PMID: 32621863      PMCID: PMC7376089          DOI: 10.1016/j.bpj.2020.05.032

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


  13 in total

1.  Fluorescence-intensity distribution analysis and its application in biomolecular detection technology.

Authors:  P Kask; K Palo; D Ullmann; K Gall
Journal:  Proc Natl Acad Sci U S A       Date:  1999-11-23       Impact factor: 11.205

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

Review 3.  Imaging with total internal reflection fluorescence microscopy for the cell biologist.

Authors:  Alexa L Mattheyses; Sanford M Simon; Joshua Z Rappoport
Journal:  J Cell Sci       Date:  2010-11-01       Impact factor: 5.285

4.  A closed form for fluorescence correlation spectroscopy experiments in submicrometer structures.

Authors:  Luigi Sanguigno; Ilaria De Santo; Filippo Causa; Paolo Netti
Journal:  Anal Chem       Date:  2010-11-01       Impact factor: 6.986

5.  Distribution of molecular aggregation by analysis of fluctuation moments.

Authors:  H Qian; E L Elson
Journal:  Proc Natl Acad Sci U S A       Date:  1990-07       Impact factor: 11.205

6.  Fluorescence correlation spectroscopy for detecting submicroscopic clusters of fluorescent molecules in membranes.

Authors:  A G Palmer; N L Thompson
Journal:  Chem Phys Lipids       Date:  1989-06       Impact factor: 3.329

Review 7.  Fluorescence fluctuation spectroscopy: an invaluable microscopy tool for uncovering the biophysical rules for navigating the nuclear landscape.

Authors:  David G Priest; Ashleigh Solano; Jieqiong Lou; Elizabeth Hinde
Journal:  Biochem Soc Trans       Date:  2019-07-05       Impact factor: 5.407

8.  On the analysis of high order moments of fluorescence fluctuations.

Authors:  H Qian; E L Elson
Journal:  Biophys J       Date:  1990-02       Impact factor: 4.033

9.  Myosin V walks hand-over-hand: single fluorophore imaging with 1.5-nm localization.

Authors:  Ahmet Yildiz; Joseph N Forkey; Sean A McKinney; Taekjip Ha; Yale E Goldman; Paul R Selvin
Journal:  Science       Date:  2003-06-05       Impact factor: 47.728

10.  Cell-substrate contacts illuminated by total internal reflection fluorescence.

Authors:  D Axelrod
Journal:  J Cell Biol       Date:  1981-04       Impact factor: 10.539

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