作者
Ehud Gazit, Anita Boman, Hans G Boman, Yechiel Shai
发表日期
1995/9/1
期刊
Biochemistry
卷号
34
期号
36
页码范围
11479-11488
出版商
American Chemical Society
简介
Revised Manuscript Received June 29, 1995® abstract: Cecropins are positively charged antibacterial polypeptides that were originally isolated from insects. Later on a mammalian homologue, cecropin PI (CecP), was isolated from pig intestines. While insect cecropins are highly potent against both Gram-negative and Gram-positive bacteria, CecP is as active as insect cecropins against Gram-negative but has reduced activity against Gram-positive bacteria. To gain insight into the mechanism of action of CecP and the molecular basis of its antibacterial specificity, the peptide and its proline incorporated analogue (at the conserved position found in insect cecropins), P22-CecP, were synthesized and labeled on their N-terminal amino-acids with fluorescent probes, without significantly affecting their antibacterial activities. Fluorescence studies indicated that the N-terminal of CecP is located on the surface of …
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