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AbstractAbstract
[en] The assignment of amide resonances in the two-dimensional PISEMA (Polarization Inversion with Spin Exchange at the Magic Angle) spectrum of uniformly 15N labeled M2 peptide corresponding to the channel-lining segment of the acetylcholine receptor in oriented phospholipid bilayers is described. The majority of the resonances were assigned through comparisons with spectra from selectively 15N labeled recombinant peptides and specifically 15N labeled synthetic peptides. Some resonances were assigned to specific amino acid residues by means of homonuclear 15N spin-exchange spectroscopy. A modification to the conventional spin-exchange pulse sequence that significantly shortens the length of the experiments by combining the intervals for 15 N spin-exchange and 1H magnetization recovery is described
Primary Subject
Source
Copyright (c) 1999 Kluwer Academic Publishers; Country of input: International Atomic Energy Agency (IAEA)
Record Type
Journal Article
Journal
Journal of Biomolecular NMR; ISSN 0925-2738;
; v. 14(2); p. 141-148

Country of publication
AMINES, AMMONIUM COMPOUNDS, AUTONOMIC NERVOUS SYSTEM AGENTS, CARBOXYLIC ACIDS, DRUGS, ESTERS, HYDROGEN ISOTOPES, ISOTOPES, LIGHT NUCLEI, LIPIDS, MAGNETIC RESONANCE, MEMBRANE PROTEINS, NEUROREGULATORS, NITROGEN ISOTOPES, NUCLEI, ODD-EVEN NUCLEI, ORGANIC ACIDS, ORGANIC COMPOUNDS, ORGANIC PHOSPHORUS COMPOUNDS, PARASYMPATHOMIMETICS, PROTEINS, QUATERNARY COMPOUNDS, RESONANCE, SPECTRA, STABLE ISOTOPES
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