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Using Paramagnetism to Slow Down Nuclear Relaxation in Protein NMR

dc.contributor.authorOrton, Henry W
dc.contributor.authorKuprov, Ilya
dc.contributor.authorLoh, Choy-Theng
dc.contributor.authorOtting, Gottfried
dc.date.accessioned2018-10-18T04:02:58Z
dc.date.available2018-10-18T04:02:58Z
dc.date.issued2016-12-01
dc.description.abstractParamagnetic metal ions accelerate nuclear spin relaxation; this effect is widely used for distance measurement and called paramagnetic relaxation enhancement (PRE). Theoretical predictions established that, under special circumstances, it is also possible to achieve a reduction in nuclear relaxation rates (negative PRE). This situation would occur if the mechanism of nuclear relaxation in the diamagnetic state is counterbalanced by a paramagnetic relaxation mechanism caused by the metal ion. Here we report the first experimental evidence for such a cross-correlation effect. Using a uniformly 15N-labeled mutant of calbindin D9k loaded with either Tm3+ or Tb3+, reduced R1 and R2 relaxation rates of backbone 15N spins were observed compared with the diamagnetic reference (the same protein loaded with Y3+). The effect arises from the compensation of the chemical shift anisotropy tensor by the anisotropic dipolar shielding generated by the unpaired electron spin.en_AU
dc.description.sponsorshipFinancial support by the Australian Research Council is gratefully acknowledged.en_AU
dc.format.mimetypeapplication/pdfen_AU
dc.identifier.issn1948-7185en_AU
dc.identifier.urihttp://hdl.handle.net/1885/148503
dc.publisherAmerican Chemical Societyen_AU
dc.rights© 2016 American Chemical Society. http://www.sherpa.ac.uk/romeo/issn/1948-7185/..."author can archive post-print (ie final draft post-refereeing) If mandated by funding agency or employer/ institution. 12 months embargo" from SHERPA/RoMEO site (as at 18/10/18).en_AU
dc.sourceThe journal of physical chemistry lettersen_AU
dc.subjectnuclear magnetic resonance, biomolecularen_AU
dc.subjectproteinsen_AU
dc.titleUsing Paramagnetism to Slow Down Nuclear Relaxation in Protein NMRen_AU
dc.typeJournal articleen_AU
dcterms.accessRightsOpen Accessen_AU
local.bibliographicCitation.issue23en_AU
local.bibliographicCitation.lastpage4818en_AU
local.bibliographicCitation.startpage4815en_AU
local.contributor.affiliationOtting, G., Research School of Chemistry, The Australian National Universityen_AU
local.contributor.authoruidu4046684en_AU
local.identifier.citationvolume7en_AU
local.identifier.doi10.1021/acs.jpclett.6b02417en_AU
local.identifier.essn1948-7185en_AU
local.publisher.urlhttps://pubs.acs.org/en_AU
local.type.statusAccepted Versionen_AU

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