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dc.contributor.authorMyint, Wazo
dc.contributor.authorCai, Yufeng
dc.contributor.authorSchiffer, Celia A.
dc.contributor.authorIshima, Rieko
dc.date2022-08-11T08:08:00.000
dc.date.accessioned2022-08-23T15:38:50Z
dc.date.available2022-08-23T15:38:50Z
dc.date.issued2012-05-01
dc.date.submitted2012-10-10
dc.identifier.citation<p>J Biomol NMR. 2012 May;53(1):13-23. Epub 2012 Apr 1. <a href="http://dx.doi.org/10.1007/s10858-012-9621-x" target="_blank">Link to article on publisher's site</a></p>
dc.identifier.issn0925-2738 (Linking)
dc.identifier.doi10.1007/s10858-012-9621-x
dc.identifier.pmid22466935
dc.identifier.urihttp://hdl.handle.net/20.500.14038/26021
dc.description.abstractNitrogen-15 Carr-Purcell-Meiboom-Gill (CPMG) transverse relaxation experiment are widely used to characterize protein backbone dynamics and chemical exchange parameters. Although an accurate value of the transverse relaxation rate, R(2), is needed for accurate characterization of dynamics, the uncertainty in the R(2) value depends on the experimental settings and the details of the data analysis itself. Here, we present an analysis of the impact of CPMG pulse phase alternation on the accuracy of the (15)N CPMG R(2). Our simulations show that R(2) can be obtained accurately for a relatively wide spectral width, either using the conventional phase cycle or using phase alternation when the r.f. pulse power is accurately calibrated. However, when the r.f. pulse is miscalibrated, the conventional CPMG experiment exhibits more significant uncertainties in R(2) caused by the off-resonance effect than does the phase alternation experiment. Our experiments show that this effect becomes manifest under the circumstance that the systematic error exceeds that arising from experimental noise. Furthermore, our results provide the means to estimate practical parameter settings that yield accurate values of (15)N transverse relaxation rates in the both CPMG experiments.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=22466935&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1007/s10858-012-9621-x
dc.subjectMolecular Dynamics Simulation
dc.subjectMonte Carlo Method
dc.subjectNitrogen Isotopes
dc.subjectNuclear Magnetic Resonance, Biomolecular
dc.subjectProteins
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectPharmacology, Toxicology and Environmental Health
dc.titleQuantitative comparison of errors in 15N transverse relaxation rates measured using various CPMG phasing schemes
dc.typeJournal Article
dc.source.journaltitleJournal of biomolecular NMR
dc.source.volume53
dc.source.issue1
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/bmp_pp/150
dc.identifier.contextkey3383245
html.description.abstract<p>Nitrogen-15 Carr-Purcell-Meiboom-Gill (CPMG) transverse relaxation experiment are widely used to characterize protein backbone dynamics and chemical exchange parameters. Although an accurate value of the transverse relaxation rate, R(2), is needed for accurate characterization of dynamics, the uncertainty in the R(2) value depends on the experimental settings and the details of the data analysis itself. Here, we present an analysis of the impact of CPMG pulse phase alternation on the accuracy of the (15)N CPMG R(2). Our simulations show that R(2) can be obtained accurately for a relatively wide spectral width, either using the conventional phase cycle or using phase alternation when the r.f. pulse power is accurately calibrated. However, when the r.f. pulse is miscalibrated, the conventional CPMG experiment exhibits more significant uncertainties in R(2) caused by the off-resonance effect than does the phase alternation experiment. Our experiments show that this effect becomes manifest under the circumstance that the systematic error exceeds that arising from experimental noise. Furthermore, our results provide the means to estimate practical parameter settings that yield accurate values of (15)N transverse relaxation rates in the both CPMG experiments.</p>
dc.identifier.submissionpathbmp_pp/150
dc.contributor.departmentDepartment of Biochemistry and Molecular Pharmacology
dc.source.pages13-23


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