Peptide Scanning for Studying Structure-Activity Relationships in Drug Discovery

被引:75
作者
Jamieson, Andrew G. [2 ]
Boutard, Nicolas [3 ]
Sabatino, David [4 ]
Lubell, William D. [1 ]
机构
[1] Univ Montreal, Dept Chem, Montreal, PQ H3C 3J7, Canada
[2] Univ Leicester, Dept Chem, Leicester LE1 7RH, Leics, England
[3] Italian Inst Technol, Drug Discovery & Dev Dept, I-16163 Genoa, Italy
[4] Seton Hall Univ, Dept Chem & Biochem, S Orange, NJ 07079 USA
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
aza-amino acid; conformational constraint; Freidinger lactam; peptidomimetic; scan; stapled peptide; SOLID-PHASE SYNTHESIS; PROTEIN-PROTEIN INTERACTIONS; AZAAMINO ACID RESIDUE; HUMAN GROWTH-HORMONE; D-AMINO-ACID; SECONDARY STRUCTURE; N-METHYLATION; BINDING-SITE; AZA-PEPTIDES; LACTAM PEPTIDOMIMETICS;
D O I
10.1111/cbdd.12042
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
Peptide-based therapeutics have grown in importance over the last few decades. Furthermore, peptides have been extensively used as lead compounds in the drug discovery process to investigate the nature of chemical space required for molecular recognition and activity at a variety of targets. This critical commentary reviews scanning techniques, which employ natural and non-proteinogenic amino acids to facilitate understanding of structural requirements for peptide biological activity. The value of sequence analysis by such methods is highlighted by examples, in which the elements for peptide affinity and activity have been elucidated and employed to prepare peptidomimetic leads for drug development.
引用
收藏
页码:148 / 165
页数:18
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