Breaking the Concentration Limit in Fluorescence Fluctuation Spectroscopy with Camera-Based Detection.

fluorescence fluctuation spectroscopy image correlation spectroscopy light sheet microscopy molecular interactions

Journal

International journal of molecular sciences
ISSN: 1422-0067
Titre abrégé: Int J Mol Sci
Pays: Switzerland
ID NLM: 101092791

Informations de publication

Date de publication:
30 Aug 2022
Historique:
received: 08 08 2022
revised: 23 08 2022
accepted: 26 08 2022
entrez: 9 9 2022
pubmed: 10 9 2022
medline: 14 9 2022
Statut: epublish

Résumé

Fluorescence correlation spectroscopy (FCS) is an extremely versatile tool that has been widely used to measure chemical reaction rates, protein binding, nanoparticle-protein interactions, and biomolecular dynamics in vitro and in vivo. As an inherently micro-sized approach, FCS is compatible with high-throughput screening applications, as demanded for drug design, but typically limited to nanomolar concentrations, which restricts possible applications. Here, we show how massively parallel camera-based detection with side illumination can extend the usable concentration range of FCS more than 100-fold to measure low affinity processes. Our line illumination (LIM) approach is robust, fast (1 s acquisition times), and does not require any reference measurements to characterize the observation volume size.

Identifiants

pubmed: 36077237
pii: ijms23179840
doi: 10.3390/ijms23179840
pmc: PMC9456017
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Subventions

Organisme : NIGMS NIH HHS
ID : R21GM135493
Pays : United States

Références

Mol Immunol. 2012 Oct;52(3-4):174-82
pubmed: 22677715
Biophys Rev. 2009 Sep 1;1(3):105-118
pubmed: 21547245
Biochim Biophys Acta. 2002 Sep 23;1599(1-2):141-8
pubmed: 12479415
Biopolymers. 1974 Jan;13(1):29-61
pubmed: 4818131
ACS Chem Neurosci. 2022 Apr 6;13(7):876-882
pubmed: 35319179
Opt Express. 2006 Jan 23;14(2):956-69
pubmed: 19503416
Opt Express. 2005 Sep 5;13(18):7035-44
pubmed: 19498725
Nat Commun. 2013;4:2093
pubmed: 23803641
Sci Rep. 2014 Nov 14;4:7048
pubmed: 25394360
J Fluoresc. 2008 Nov;18(6):1093-101
pubmed: 18431548
Proc Natl Acad Sci U S A. 2013 Jul 23;110(30):12307-12
pubmed: 23836651
J Phys Chem B. 2014 Aug 14;118(32):9662-7
pubmed: 25060197
Analyst. 2015 Feb 21;140(4):1207-14
pubmed: 25526365
Biomed Opt Express. 2017 Aug 01;8(9):3918-3937
pubmed: 29026679
Talanta. 2015 Jan;132:894-901
pubmed: 25476394
Nature. 2009 Feb 26;457(7233):1159-62
pubmed: 19098897

Auteurs

Yu-Kai Huang (YK)

Laboratory for Fluorescence Dynamics, University of California Irvine, Irvine, CA 92697, USA.

Per Niklas Hedde (PN)

Laboratory for Fluorescence Dynamics, University of California Irvine, Irvine, CA 92697, USA.
Beckman Laser Institute and Medical Clinic, University of California Irvine, Irvine, CA 92697, USA.
Department of Pharmaceutical Sciences, University of California Irvine, Irvine, CA 92697, USA.

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Classifications MeSH