Peptides Containing β-Amino Acid Patterns: Challenges and Successes in Medicinal Chemistry

被引:267
|
作者
Cabrele, Chiara [1 ]
Martinek, Tamas A. [2 ]
Reiser, Oliver [3 ]
Berlicki, Lukasz [4 ]
机构
[1] Salzburg Univ, Dept Mol Biol, A-5020 Salzburg, Austria
[2] Univ Szeged, Inst Pharmaceut Anal, SZTE MTA Lendulet Foldamer Res Grp, H-6720 Szeged, Hungary
[3] Univ Regensburg, Inst Organ Chem, D-93053 Regensburg, Germany
[4] Wroclaw Univ Technol, Fac Chem, Dept Bioorgan Chem, Wybrzeze Wyspianskiego 27, PL-50370 Wroclaw, Poland
关键词
DE-NOVO DESIGN; ALPHA-HELIX MIMICRY; PROTEIN-PROTEIN INTERACTIONS; HUMAN SOMATOSTATIN RECEPTOR; GENE-RELATED PEPTIDE; NEUROPEPTIDE-Y; ENDOMORPHIN-1; ANALOGS; CELL PENETRATION; GAMMA-SECRETASE; BETA(3)-PEPTIDE INHIBITORS;
D O I
10.1021/jm5010896
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The construction of bioactive peptides using beta-amino acid-containing sequence patterns is a very promising strategy to obtain analogues that exhibit properties of high interest for medicinal chemistry applications. beta-Amino acids have been shown to modulate the conformation, dynamics, and proteolytic susceptibility of native peptides. They can be either combined with alpha-amino acids by following specific patterns, which results in backbone architectures with well-defined orientations of the side chain functional groups, or assembled in de novo-designed bioactive beta- or alpha,beta-peptidic sequences. Such peptides display various biological functions, including antimicrobial activity, inhibition of proteinprotein interactions, agonism/antagonism of GPCR ligands, and anti-angiogenic activity.
引用
收藏
页码:9718 / 9739
页数:22
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