Using Paramagnetism to Slow Down Nuclear Relaxation in Protein NMR
| dc.contributor.author | Orton, Henry W | |
| dc.contributor.author | Kuprov, Ilya | |
| dc.contributor.author | Loh, Choy-Theng | |
| dc.contributor.author | Otting, Gottfried | |
| dc.date.accessioned | 2018-10-18T04:02:58Z | |
| dc.date.available | 2018-10-18T04:02:58Z | |
| dc.date.issued | 2016-12-01 | |
| dc.description.abstract | Paramagnetic 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.sponsorship | Financial support by the Australian Research Council is gratefully acknowledged. | en_AU |
| dc.format.mimetype | application/pdf | en_AU |
| dc.identifier.issn | 1948-7185 | en_AU |
| dc.identifier.uri | http://hdl.handle.net/1885/148503 | |
| dc.publisher | American Chemical Society | en_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.source | The journal of physical chemistry letters | en_AU |
| dc.subject | nuclear magnetic resonance, biomolecular | en_AU |
| dc.subject | proteins | en_AU |
| dc.title | Using Paramagnetism to Slow Down Nuclear Relaxation in Protein NMR | en_AU |
| dc.type | Journal article | en_AU |
| dcterms.accessRights | Open Access | en_AU |
| local.bibliographicCitation.issue | 23 | en_AU |
| local.bibliographicCitation.lastpage | 4818 | en_AU |
| local.bibliographicCitation.startpage | 4815 | en_AU |
| local.contributor.affiliation | Otting, G., Research School of Chemistry, The Australian National University | en_AU |
| local.contributor.authoruid | u4046684 | en_AU |
| local.identifier.citationvolume | 7 | en_AU |
| local.identifier.doi | 10.1021/acs.jpclett.6b02417 | en_AU |
| local.identifier.essn | 1948-7185 | en_AU |
| local.publisher.url | https://pubs.acs.org/ | en_AU |
| local.type.status | Accepted Version | en_AU |