Design and development of peptides and peptide mimetics as antagonists for therapeutic intervention

被引:105
作者
Mason, Jody M. [1 ]
机构
[1] Univ Essex, Dept Biol Sci, Colchester CO4 3SQ, Essex, England
基金
英国惠康基金;
关键词
IMAGE PHAGE DISPLAY; IN-VITRO SELECTION; PROTEIN-PROTEIN INTERACTIONS; CELL-PENETRATING PEPTIDES; BETA-AMYLOID AGGREGATION; HYDROGEN-BOND-SURROGATE; C-CAPPING PREFERENCES; FLUORESCENCE COMPLEMENTATION; ALZHEIMERS-DISEASE; RIBOSOME DISPLAY;
D O I
10.4155/FMC.10.259
中图分类号
R914 [药物化学];
学科分类号
100705 [微生物与生化药学];
摘要
The concept of peptides as therapeutic agents has been historically disregarded by the pharmaceutical industry on account of their susceptibility to degradation, their size and consequent limitations in methods of delivery. Recently, however, there has been a surge of interest in peptides and their mimetics as potential antagonists for therapeutic intervention. This is in part due to the increased half-life and oral availability that has been achieved for a number of peptide-based systems, the introduction and acceptance of alternative delivery methods, and the prevalence of proteomics to identify countless protein-protein interaction targets. The use of peptides and molecules that mimic their function therefore has great potential to effectively target a range of proteins that are pathogenically implicated in numerous diseases.
引用
收藏
页码:1813 / 1822
页数:10
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