SPECTROSCOPIC STUDIES ON CONFORMATION OF GRAMICIDIN A' - PROTON MAGNETIC-RESONANCE ASSIGNMENTS, COUPLING-CONSTANTS, AND H-D EXCHANGE
SPECTROSCOPIC STUDIES ON CONFORMATION OF GRAMICIDIN A' - PROTON MAGNETIC-RESONANCE ASSIGNMENTS, COUPLING-CONSTANTS, AND H-D EXCHANGE
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DOI:
10.1021/bi00754a001
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发表时间:
1972-01-01
期刊:
影响因子:
2.9
通讯作者:
SETTINE, JM
中科院分区:
文献类型:
--
作者:
GLICKSON, JD;MAYERS, DF;SETTINE, JM
J. D. Glickson, D. F. Mayers, J. M. Settine, and D. W. Urryf abstract: Analysis of proton magnetic resonances of a commercial preparation (Nutritional Biochemicals) of gramicidin, referred to herein as gramicidin A'(GA'), shows the preparation to contain gramicidin A (GA), gramicidin B (GB), and gramicidin C (GC) in ratios of 72: 9: 19, respec-tively. These gramicidins differ only in the amino acid at position 11. The analysis isbased on the relative intensities of tryptophan indole CH resonances, the phenylalanine phenyl CH resonance(of GB), and the tyrosine ortho CH resonance(of GC). Resonances in the 220-MHz proton magnetic resonance spectrum of GA'in hexadeuteriodimethyl sulfoxide (Me2SO-tif6) are assigned to specific hydrogens. An ordered conformation is indicated by the following evidence, all of which is consistent with the ttl. d helices previously proposed for the structure of GA'in transmembranechannels (Urry, D. W.(1971), Proc. Nat. Acad. Sci. US 68, 672; Urry, D. W., Goodall, M. C., Glickson, J. D., and Mayers, D. F.(1971a), Proc. Nat. Acad. Sci. US 68, 1907).(1) Observation of distinct resonances from side-chain protons that are chemically equivalent except for the sequence posi-