SHORTENED CECROPIN-A MELITTIN HYBRIDS - SIGNIFICANT SIZE-REDUCTION RETAINS POTENT ANTIBIOTIC-ACTIVITY

被引:249
作者
ANDREU, D
UBACH, J
BOMAN, A
WAHLIN, B
WADE, D
MERRIFIELD, RB
BOMAN, HG
机构
[1] UNIV STOCKHOLM,DEPT IMMUNOL,S-10691 STOCKHOLM,SWEDEN
[2] UNIV STOCKHOLM,DEPT MICROBIOL,S-10691 STOCKHOLM,SWEDEN
[3] ROCKEFELLER UNIV,NEW YORK,NY 10021
关键词
ANTIBACTERIAL PEPTIDE; CECROPIN-A; MELITTIN; SOLID-PHASE PEPTIDE SYNTHESIS;
D O I
10.1016/0014-5793(92)80377-S
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
We have earlier reported two 26-residue antibacterial peptides made up from different segments of cecropin A (CA) and melittin (M). We now report a substantial reduction in size at the C-terminal section of the highly active hybrid CA(1-8)M(1-18), leading to a series of 20-, 18- and 15-residue analogs with antibiotic properties similar to the larger molecule. In particular, the 15-residue hybrids CA(1-7)M(2-9), CA(1-7)M(4-11) and CA(1-7)M(5-12) are the shortest cecropin-based peptide antibiotics described so far, with antibacterial activity and spectra similar or better than cecropin A and a 60% reduction in size. Their reduced size and highly alpha-helical structure require an alternative mechanism for their interaction with bacterial membranes.
引用
收藏
页码:190 / 194
页数:5
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