Monitoring Proton Exchange and Triplet States with Fluorescence

Fluorescent molecules commonly shift to transient dark states, induced bylight or triggered by chemical reactions. The transient dark states can beused as probes of the local environment surrounding the fluorescent molecules,and are therefore attractive for use in biomolecular applications. Thisthes...

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Main Author: Sandén, Tor
Format: Doctoral Thesis
Language:English
Published: KTH, Experimentell biomolekylär fysik 2009
Subjects:
Online Access:http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-10400
http://nbn-resolving.de/urn:isbn:978-91-7415-304-0
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spelling ndltd-UPSALLA1-oai-DiVA.org-kth-104002013-01-08T13:07:01ZMonitoring Proton Exchange and Triplet States with FluorescenceengSandén, TorKTH, Experimentell biomolekylär fysikStockholm : KTH2009fluorescence correlation spectroscopyproton transfercytochrome c oxidasetransient state imagingmodulated excitationOpticsOptikBiochemistryBiokemiFluorescent molecules commonly shift to transient dark states, induced bylight or triggered by chemical reactions. The transient dark states can beused as probes of the local environment surrounding the fluorescent molecules,and are therefore attractive for use in biomolecular applications. Thisthesis explores the use and development of novel fluorescence spectroscopictechniques for monitoring transient dark states.This work demonstrates that kinetic information regarding photoinduced transient dark states of fluorescent molecules can be obtained from the time-averaged fluorescence intensity of fluorescent molecules subject totemporally modulated illumination. Methods based on this approach havethe advantage that the light detectors can have a low time resolution, which allows for parallelization and screening of biomolecular interactions withhigh throughput. Transient state images are presented displaying local environmental differences such as those in oxygen concentration and quencher accessibility.Analysis of the fluorescence intensity fluctuations resulting from thetransitions to and from transient dark states can be used to obtain information regarding the transition rates and occupancy of the transient darkstates. Fluorescence fluctuation analysis was used to reveal rates of protonbinding and debinding to single fluorescent molecules located close to biological membranes and protein surfaces. The results from these studies show that the proton exchange rate increases dramatically when the fluorescent molecule is close to the membrane. QC 20100809Doctoral thesis, comprehensive summaryinfo:eu-repo/semantics/doctoralThesistexthttp://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-10400urn:isbn:978-91-7415-304-0Trita-FYS, 0280-316X ; 2009:14application/pdfinfo:eu-repo/semantics/openAccess
collection NDLTD
language English
format Doctoral Thesis
sources NDLTD
topic fluorescence correlation spectroscopy
proton transfer
cytochrome c oxidase
transient state imaging
modulated excitation
Optics
Optik
Biochemistry
Biokemi
spellingShingle fluorescence correlation spectroscopy
proton transfer
cytochrome c oxidase
transient state imaging
modulated excitation
Optics
Optik
Biochemistry
Biokemi
Sandén, Tor
Monitoring Proton Exchange and Triplet States with Fluorescence
description Fluorescent molecules commonly shift to transient dark states, induced bylight or triggered by chemical reactions. The transient dark states can beused as probes of the local environment surrounding the fluorescent molecules,and are therefore attractive for use in biomolecular applications. Thisthesis explores the use and development of novel fluorescence spectroscopictechniques for monitoring transient dark states.This work demonstrates that kinetic information regarding photoinduced transient dark states of fluorescent molecules can be obtained from the time-averaged fluorescence intensity of fluorescent molecules subject totemporally modulated illumination. Methods based on this approach havethe advantage that the light detectors can have a low time resolution, which allows for parallelization and screening of biomolecular interactions withhigh throughput. Transient state images are presented displaying local environmental differences such as those in oxygen concentration and quencher accessibility.Analysis of the fluorescence intensity fluctuations resulting from thetransitions to and from transient dark states can be used to obtain information regarding the transition rates and occupancy of the transient darkstates. Fluorescence fluctuation analysis was used to reveal rates of protonbinding and debinding to single fluorescent molecules located close to biological membranes and protein surfaces. The results from these studies show that the proton exchange rate increases dramatically when the fluorescent molecule is close to the membrane. === QC 20100809
author Sandén, Tor
author_facet Sandén, Tor
author_sort Sandén, Tor
title Monitoring Proton Exchange and Triplet States with Fluorescence
title_short Monitoring Proton Exchange and Triplet States with Fluorescence
title_full Monitoring Proton Exchange and Triplet States with Fluorescence
title_fullStr Monitoring Proton Exchange and Triplet States with Fluorescence
title_full_unstemmed Monitoring Proton Exchange and Triplet States with Fluorescence
title_sort monitoring proton exchange and triplet states with fluorescence
publisher KTH, Experimentell biomolekylär fysik
publishDate 2009
url http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-10400
http://nbn-resolving.de/urn:isbn:978-91-7415-304-0
work_keys_str_mv AT sandentor monitoringprotonexchangeandtripletstateswithfluorescence
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