Spectroscopic selection of distance measurements in a protein dimer with mixed nitroxide and Gd 3+ spin labels

dc.contributor.authorKaminker, Iliaen_AU
dc.contributor.authorYagi, Hiromasaen_AU
dc.contributor.authorFeintuch, Akivaen_AU
dc.contributor.authorGoldfarb, Daniellaen_AU
dc.contributor.authorOtting, Gottfrieden_AU
dc.contributor.authorHuber, Thomasen_AU
dc.date.accessioned2015-12-10T22:59:08Z
dc.date.issued2012
dc.date.updated2016-02-24T10:25:06Z
dc.description.abstractThe pulse DEER (Double Electron-Electron Resonance) technique is frequently applied for measuring nanometer distances between specific sites in biological macromolecules. In this work we extend the applicability of this method to high field distance measurements in a protein assembly with mixed spin labels, i.e. a nitroxide spin label and a Gd 3+ tag. We demonstrate the possibility of spectroscopic selection of distance distributions between two nitroxide spin labels, a nitroxide spin label and a Gd 3+ ion, and two Gd 3+ ions. Gd 3+-nitroxide DEER measurements possess high potential for W-band long range distance measurements (6 nm) by combining high sensitivity with ease of data analysis, subject to some instrumental improvements.
dc.identifier.issn1463-9076
dc.identifier.urihttp://hdl.handle.net/1885/60958
dc.publisherRoyal Society of Chemistry
dc.sourcePhysical Chemistry Chemical Physics
dc.subjectKeywords: gadolinium; heat shock protein; nitrogen oxide; article; chemical structure; chemistry; dimerization; electron spin resonance; spin labeling; Dimerization; Electron Spin Resonance Spectroscopy; Gadolinium; Heat-Shock Proteins; Models, Molecular; Molecular
dc.titleSpectroscopic selection of distance measurements in a protein dimer with mixed nitroxide and Gd 3+ spin labels
dc.typeJournal article
local.bibliographicCitation.issue13
local.bibliographicCitation.lastpage4358
local.bibliographicCitation.startpage4355
local.contributor.affiliationKaminker, Ilia, Weizmann Institute of Science
local.contributor.affiliationYagi, Hiromasa, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationHuber, Thomas, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationFeintuch, Akiva, Weizmann Institute of Science
local.contributor.affiliationOtting, Gottfried, College of Physical and Mathematical Sciences, ANU
local.contributor.affiliationGoldfarb, Daniella, Weizmann Institute of Science
local.contributor.authoruidYagi, Hiromasa, u4564668
local.contributor.authoruidHuber, Thomas, u9512183
local.contributor.authoruidOtting, Gottfried, u4046684
local.description.embargo2037-12-31
local.description.notesImported from ARIES
local.identifier.absfor030402 - Biomolecular Modelling and Design
local.identifier.absfor030403 - Characterisation of Biological Macromolecules
local.identifier.absfor030406 - Proteins and Peptides
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciences
local.identifier.ariespublicationu4005981xPUB576
local.identifier.citationvolume14
local.identifier.doi10.1039/c2cp40219j
local.identifier.scopusID2-s2.0-84858402344
local.identifier.thomsonID000301235200007
local.type.statusPublished Version

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