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Nanometer-range distance measurement in a protein using Mn 2+ tags

dc.contributor.authorBanerjee, Debamalyaen_AU
dc.contributor.authorYagi, Hiromasaen_AU
dc.contributor.authorGoldfarb, Daniellaen_AU
dc.contributor.authorOtting, Gottfrieden_AU
dc.contributor.authorHuber, Thomasen_AU
dc.date.accessioned2015-12-10T22:58:12Z
dc.date.issued2012
dc.date.updated2016-02-24T10:24:46Z
dc.description.abstractPulse electron paramagnetic resonance measurements of long-range (nm scale) distances between spin labels site-specifically attached to biomacromolecules have proven highly effective in structural studies. The most commonly used spin labels are stable nitroxide radicals, and measurements are usually carried out at X-band frequencies (∼9.5 GHz, 0.35 T). Higher magnetic fields open new possibilities for distance measurements with increased sensitivity using alternative spin labels containing half-integer high-spin metal ions. Here we demonstrate W-band (95 GHz) pulse double electron-electron resonance (DEER) distance measurements in a protein labeled with two Mn2+-EDTA tags. The distance distribution obtained is in excellent agreement with model calculations based on the known solution NMR structure. Thus, site-specific labeling with Mn2+ tags opens a highly promising approach to nanometer distance measurements in biological macromolecules.
dc.identifier.issn1948-7185
dc.identifier.urihttp://hdl.handle.net/1885/60756
dc.publisherAmerican Chemical Society
dc.sourceJournal of Physical Chemistry Letters
dc.subjectKeywords: Biological macromolecule; Biomacromolecules; Distance distributions; Double electron-electron resonance; Model calculations; Nitroxide radicals; Site-specific; Solution NMR; Spin label; Structural studies; X-band frequencies; Electron resonance; Magnetic
dc.titleNanometer-range distance measurement in a protein using Mn 2+ tags
dc.typeJournal article
local.bibliographicCitation.issue2
local.bibliographicCitation.lastpage160
local.bibliographicCitation.startpage157
local.contributor.affiliationBanerjee, Debamalya, 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.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.absfor030403 - Characterisation of Biological Macromolecules
local.identifier.absfor030406 - Proteins and Peptides
local.identifier.absfor030402 - Biomolecular Modelling and Design
local.identifier.absseo970103 - Expanding Knowledge in the Chemical Sciences
local.identifier.absseo970106 - Expanding Knowledge in the Biological Sciences
local.identifier.ariespublicationu4005981xPUB561
local.identifier.citationvolume3
local.identifier.doi10.1021/jz201521d
local.identifier.scopusID2-s2.0-84856002857
local.identifier.thomsonID000299365500003
local.type.statusPublished Version

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