拓展生物活性肽的拓扑空间。
Expanding the topological space of bioactive peptides.
作者信息
Reymond Jean-Louis, Darbre Tamis
机构信息
Department of Chemistry and Biochemistry, University of Bern, Freiestrasse 3, CH-3012 Bern, Switzerland.
出版信息
Chimia (Aarau). 2013;67(12-13):864-7. doi: 10.2533/chimia.2013.864.
Naturally occurring peptides and proteins consist almost exclusively of linear or cyclic polypeptide chains. Our group explores the chemical space of peptides by redesigning their topology through the introduction of branching points in the peptide chain. Branched peptides are generally resistant to proteolysis and display remarkable biological properties by multivalency effects (peptide dendrimers) and conformational rigidity (polycyclic peptides). We review our recent progress in peptide dendrimers as enzyme models, biofilm inhibitors, antimicrobials, DNA transfection and cell-penetrating agents, and in the synthesis and characterization of bicyclic peptides as new scaffolds for drug design.
天然存在的肽和蛋白质几乎完全由线性或环状多肽链组成。我们的研究小组通过在肽链中引入分支点来重新设计其拓扑结构,从而探索肽的化学空间。分支肽通常对蛋白水解具有抗性,并通过多价效应(肽树枝状大分子)和构象刚性(多环肽)表现出显著的生物学特性。我们综述了我们在作为酶模型、生物膜抑制剂、抗菌剂、DNA转染剂和细胞穿透剂的肽树枝状大分子方面的最新进展,以及作为药物设计新支架的双环肽的合成和表征。