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Gd3 + Spin Labeling for Measuring Distances in Biomacromolecules

dc.contributor.authorFeintuch, Akivaen
dc.contributor.authorOtting, Gottfrieden
dc.contributor.authorGoldfarb, Daniellaen
dc.date.accessioned2025-05-27T21:20:32Z
dc.date.available2025-05-27T21:20:32Z
dc.date.issued2015en
dc.description.abstractApplications of distance measurements by pulse dipolar electron-paramagnetic resonance (PD-EPR) spectroscopy to structural biology are based on introducing spin labels (SLs) at well-defined locations in the biomacromolecule. The most commonly used SLs are nitroxyl radicals, but recently SLs based on high-spin Gd3 + (S = 7/2) complexes have been shown to be an attractive alternative for PD-EPR, particularly double electron-electron resonance (DEER), at spectrometer frequencies higher than 30 GHz. In this chapter, we describe the advantage of using this new family of SLs in terms of sensitivity, stability, and chemical diversity. We present current labeling strategies for proteins, discuss the approximations under which DEER data analysis of a pair of Gd3 + SLs (GdSLs) is equivalent to that of a pair of S = 1/2 SLs, and discuss the reduction in multispin effects in a cluster of GdSLs, as opposed to a cluster of nitroxide labels, which can be found in oligomeric systems. In addition, we provide a brief overview of the current, rather limited, knowledge of Gd3 + phase relaxation behavior and describe experimental strategies in terms of optimizing sensitivity. The possibility of using several types of SLs in a system allows one to isolate effects due to the chemical nature of the SL itself; several such examples are presented, focusing on comparing nitroxide and GdSLs. Finally, we will discuss the initial results on in-cell DEER with GdSLs.en
dc.description.sponsorshipFinancial support by the ISF (Israel Science Foundation), the BSF (USA-Israel bi-national science foundation), the Australian Research Council, and an Australia-Weizmann Making Connections grant are gratefully acknowledged. In part, this research was made possible by the historic generosity of the Harold Perlman family. D.G. holds the Erich Klieger Professorial Chair in Chemical Physics.en
dc.description.statusPeer-revieweden
dc.format.extent43en
dc.identifier.issn0076-6879en
dc.identifier.otherScopus:84944355772en
dc.identifier.otherPubMed:26478494en
dc.identifier.otherARIES:U3488905xPUB5818en
dc.identifier.urihttp://www.scopus.com/inward/record.url?scp=84944355772&partnerID=8YFLogxKen
dc.identifier.urihttps://dspace-test.anu.edu.au/handle/1885/733758774
dc.language.isoenen
dc.publisherAcademic Press Inc.en
dc.relation.ispartofseriesMethods in Enzymologyen
dc.rightsPublisher Copyright: © 2015 Elsevier Inc.en
dc.subjectDEERen
dc.subjectDistance measurementsen
dc.subjectEPR spectroscopyen
dc.subjectGd tagsen
dc.subjectHigh-field EPRen
dc.subjectSpin labelsen
dc.titleGd3 + Spin Labeling for Measuring Distances in Biomacromoleculesen
dc.typeBook chapteren
local.bibliographicCitation.lastpage457en
local.bibliographicCitation.startpage415en
local.contributor.affiliationFeintuch, Akiva; Weizmann Institute of Scienceen
local.contributor.affiliationOtting, Gottfried; Wearable and Portable Devices, Research School of Chemistry, ANU College of Science and Medicine, The Australian National Universityen
local.contributor.affiliationGoldfarb, Daniella; Weizmann Institute of Scienceen
local.identifier.doi10.1016/bs.mie.2015.07.006en
local.identifier.essn1557-7988en
local.identifier.pure2164a90a-dad5-4fac-9479-83cd3a42971aen
local.type.statusPublisheden

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