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001-es BibID:	BIBFORM058873
Első szerző:	Kiraly, Peter
Cím:	Real-time pure shift 15N HSQC of proteins : a real improvement in resolution and sensitivity / Peter Kiraly, Ralph W. Adams, Liladhar Paudel, Mohammadali Foroozandeh, Juan A. Aguilar, István Timári, Matthew J. Cliff, Mathias Nilsson, Péter Sándor, Gyula Batta, Jonathan P. Waltho, Katalin E. Kövér, Gareth A. Morris
Dátum:	2015
ISSN:	0925-2738
Megjegyzések:	Spectral resolution in proton NMR spectroscopy is reduced by the splitting of resonances into multiplets due to the effect of homonuclear scalar couplings. Although these effects are often hidden in protein NMR spectroscopy by low digital resolution and routine apodization, behind the scenes homonuclear scalar couplings increase spectral overcrowding. The possibilities for biomolecular NMR offered by new pure shift NMR methods are illustrated here. Both resolution and sensitivity are improved, without any increase in experiment time. In these experiments, free induction decays are collected in short bursts of data acquisition, with durations short on the timescale of J-evolution, interspersed with suitable refocusing elements. The net effect is real-time (t2) broadband homodecoupling, suppressing the multiplet structure caused by proton?proton interactions. The key feature of the refocusing elements is that they discriminate between the resonances of active (observed) and passive (coupling partner) spins. This can be achieved either by using band-selective refocusing or by the BIRD element, in both cases accompanied by a nonselective 180? proton pulse. The latter method selects the active spins based on their one-bond heteronuclear J-coupling to 15N, while the former selects a region of the 1H spectrum. Several novel pure shift experiments are presented, and the improvements in resolution and sensitivity they provide are evaluated for representative samples: the N-terminal domain of PGK; ubiquitin; and two mutants of the small antifungal protein PAF. These new experiments, delivering improved sensitivity and resolution, have the potential to replace the current standard HSQC experiments.
Tárgyszavak:	Természettudományok Kémiai tudományok idegen nyelvű folyóiratközlemény külföldi lapban Pure shift Real-time HSQC Homodecoupling Protein
Megjelenés:	Journal of Biomolecular Nmr. - 62 : 1 (2015), p. 43-52. -
További szerzők:	Adams, Ralph W. Paudel, Liladhar Foroozandeh, Mohammadali Aguilar, Juan A. Timári István (1989-) (vegyész) Cliff, Matthew J. Nilsson, Mathias Sándor Péter Batta Gyula (1953-) (molekula-szerkezet kutató) Waltho, Jonathan P. Kövér Katalin, E. (1956-2023) (vegyész) Morris, Gareth A.
Pályázati támogatás:	K 105459, ANN 110821 OTKA TÁMOP-4.2.4.A/2-11-1-2012-0001 TÁMOP TÁMOP-4.2.2.A-11/1/KONV-2012-0025 TÁMOP
Internet cím:	Szerző által megadott URL DOI Intézményi repozitóriumban (DEA) tárolt változat
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