Conformational preferences and binding to neurophysins of oxytocin analogs with sarcosine or N-methylalanine in position 7.
Conformational preferences and binding to neurophysins of oxytocin analogs with sarcosine or N-methylalanine in position 7.
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DOI:
10.1111/j.1399-3011.1985.tb02188.x
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发表时间:
2009-01
期刊:
影响因子:
--
通讯作者:
Z. Grzonka;P. K. Mishra;A. Bothner-by
中科院分区:
文献类型:
--
作者:
Z. Grzonka;P. K. Mishra;A. Bothner-by
The 600 MHz proton n.m.r. spectra of (sarcosyl7)-oxytocin and (N-methylalanyl7) oxytocin in 2H2O solution have been recorded and completely assigned. In each case the spectrum indicates the presence of two slowly interconverting conformers, which are the cis-trans isomers about the peptide bond between residues six and seven. The trans isomer is energetically favored in both cases. When neurophysin is added to a solution of (N-methylalanyl7) oxytocin or (sacrosyl7)-oxytocin at pH 3.0, the proportion of minor conformer remains constant, indicating that the cis and trans conformers are equally tightly bound to the protein.