NEUROPEPTIDE-Y - IDENTIFICATION OF THE BINDING-SITE

被引:0
|
作者
BECKSICKINGER, AG
GAIDA, W
SCHNORRENBERG, G
LANG, R
JUNG, G
机构
[1] UNIV TUBINGEN,INST ORGAN CHEM,MORGENSTELLE 18,W-7400 TUBINGEN 1,GERMANY
[2] BOEHRINGER INGELHEIM KG,DEPT PHARMACOL,W-6507 INGELHEIM,GERMANY
[3] BOEHRINGER INGELHEIM KG,DEPT MED CHEM,W-6507 INGELHEIM,GERMANY
[4] UNIV HEIDELBERG,INST PHARMACOL,W-6900 HEIDELBERG,GERMANY
来源
INTERNATIONAL JOURNAL OF PEPTIDE AND PROTEIN RESEARCH | 1990年 / 36卷 / 06期
关键词
DELETION ANALOGS; MULTIPLE PEPTIDE SYNTHESIS; NEUROPEPTIDE-Y; RECEPTOR BINDING;
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Based on the hypothetical 3D structure of neuropeptide Y (NPY), NPY 1-4-Aca-25-36, a 17 amino acid analogue, has been synthesized replacing the sequence NPY 5-24 by xi-aminocaproic acid (Aca). This low-molecular weight deletion analogue showed nearly comparable receptor affinity to NPY. In order to elucidate the structural requirements for receptor recognition each amino acid of 1-4-Aca-25-36 was exchanged by its D-enantiomer, glycine and L-alanine. In addition distinct amino acids were replaced by closely related residues. Multiple peptide synthesis was applied using Fmoc-strategy and BOP activation. Binding assay was performed on rabbit kidney membrane preparations. The results of structure affinity studies suggest that the C-terminal tetrapeptide NPY 33-36 is essential for receptor recognition.
引用
收藏
页码:522 / 530
页数:9
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