dc.contributor.author
Nieder, Jana
dc.contributor.author
Hussels, Martin
dc.contributor.author
Bittl, Robert
dc.contributor.author
Brecht, Marc
dc.date.accessioned
2018-06-08T03:12:24Z
dc.date.available
2016-06-30T05:57:27.818Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/14686
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-18877
dc.description.abstract
The accumulation of organic co-solvents in cells is a basic strategy for
organisms from various species to increase stress tolerance in extreme
environments. Widespread representatives of this class of co-solvents are
trimethylamine-N-oxide (TMAO) and betaine; these small molecules are able to
stabilize the native conformation of proteins and prevent their aggregation.
Despite their importance, detailed experimental studies on the impact of these
co-solvents on the energy landscape of proteins have not yet been carried out.
We use single-molecule spectroscopy at cryogenic temperatures to examine the
influence of these physiological relevant co-solvents on photosystem I (PSI)
from Thermosynechococcus elongatus. In contrast to PSI ensemble spectra, which
are almost unaffected by the addition of TMAO and betaine, statistical
analysis of the fluorescence emission from individual PSI trimers yields
insight into the interaction of the co-solvents with PSI. The results show an
increased homogeneity upon addition of TMAO or betaine. The number of
detectable zero-phonon lines (ZPLs) is reduced, indicating spectral diffusion
processes with faster rates. In the framework of energy landscape model these
findings indicate that co-solvents lead to reduced barrier heights between
energy valleys, and thus efficient screening of protein conformations can take
place.
en
dc.format.extent
37 Seiten
dc.rights.uri
http://www.elsevier.com/about/company-information/policies/open-access-licenses/elsevier-user-license
dc.subject.ddc
500 Naturwissenschaften und Mathematik::530 Physik
dc.title
Effect of TMAO and betaine on the energy landscape of photosystem I
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation
Biochimica et Biophysica Acta (BBA) - Bioenergetics. - 1837 (2014), 6,
S.849-856
dc.identifier.sepid
40809
dcterms.bibliographicCitation.doi
10.1016/j.bbabio.2014.01.005
dcterms.bibliographicCitation.url
http://dx.doi.org/10.1016/j.bbabio.2014.01.005
refubium.affiliation
Physik
de
refubium.affiliation.other
Institut für Experimentalphysik
refubium.mycore.fudocsId
FUDOCS_document_000000024925
refubium.resourceType.isindependentpub
no
refubium.mycore.derivateId
FUDOCS_derivate_000000006706
dcterms.accessRights.openaire
open access
dcterms.isPartOf.issn
00052728