Hydrocarbon Stapled Peptides as Modulators of Biological Function

被引:237
作者
Cromm, Philipp M. [1 ,2 ]
Spiegel, Jochen [1 ,2 ]
Grossmann, Tom N. [1 ,2 ,3 ]
机构
[1] Max Planck Inst Mol Physiol, D-44227 Dortmund, Germany
[2] Tech Univ Dortmund, Dept Chem & Chem Biol, D-44227 Dortmund, Germany
[3] Max Planck Gesell, Chem Genom Ctr, D-44227 Dortmund, Germany
关键词
PROTEIN-PROTEIN INTERACTIONS; EPIDERMAL-GROWTH-FACTOR; ALPHA-HELICAL PEPTIDES; CELL-PENETRATING PEPTIDES; C-TERMINAL-DOMAIN; ACUTE LYMPHOBLASTIC-LEUKEMIA; HIV-1 INTEGRASE INHIBITORS; CLOSING OLEFIN METATHESIS; HYDROGEN-BOND SURROGATE; FACTOR-RECEPTOR;
D O I
10.1021/cb501020r
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
070307 [化学生物学]; 071010 [生物化学与分子生物学];
摘要
Peptide-based drug discovery has experienced a significant upturn within the past decade since the introduction of chemical modifications and :unnatural amino acids has allowed for overcoming some of the drawbacks associated with peptide therapeutics. Strengthened by such features, modified peptides become capable of occupying,a niche that emerges between the two major classes of today's therapeutics-small molecules (<500 Da) and biologics (>5000 Da), Stabilized a-helices have proven particularly successful at impairing disease-relevant PPIs previously considered "undruggable.", Among those, hydrocarbon stapled alpha-helical peptides have emerged as a novel class of potential peptide therapeutics: This review provides a comprehensive overview of the development and applications of hydrocarbon stapled peptides discussing the benefits and limitations of this technique.
引用
收藏
页码:1362 / 1375
页数:14
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