Retrocyclins and their activity against HIV-1

被引:34
|
作者
Penberthy, W. Todd [1 ]
Chari, Soumya [1 ]
Cole, Amy L. [1 ]
Cole, Alexander M. [1 ]
机构
[1] Univ Cent Florida, Coll Med, Burnett Sch Biomed Sci, Dept Mol Biol & Microbiol, Orlando, FL 32816 USA
基金
美国国家卫生研究院;
关键词
Retrocyclin; Defensin; HIV-1; Host defense peptide; Antimicrobial peptide; Antiviral; Microbicide; CELL FUSION INHIBITOR; HERPES-SIMPLEX-VIRUS; ANTIMICROBIAL PEPTIDES; THETA-DEFENSINS; SYNTHETIC PEPTIDE; MARKED INCREASE; TACHYPLESIN; BINDING; RESISTANCE; INFECTION;
D O I
10.1007/s00018-011-0715-5
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
Primate theta-defensins are physically distinguished as the only known fully-cyclic peptides of animal origin. Humans do not produce theta-defensin peptides due to a premature stop codon present in the signal sequence of all six theta-defensin pseudogenes. Instead, since the putative coding regions of human theta-defensin pseudogenes have remained remarkably intact, their corresponding peptides, called "retrocyclins", have been recreated using solid-phase synthetic approaches. Retrocyclins exhibit an exceptional therapeutic index both as inhibitors of HIV-1 entry and as bactericidal agents, which makes retrocyclins promising candidates for further development as topical microbicides to prevent sexually transmitted diseases. This review presents the evolution, antiretroviral mechanism of action, and potential clinical applications of retrocyclins to prevent sexual transmission of HIV-1.
引用
收藏
页码:2231 / 2242
页数:12
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