Antimicrobial peptides from the skin of the Tsushima brown frog Rana tsushimensis

被引:35
|
作者
Conlon, JM [1 ]
Al-Ghaferi, N
Abraham, B
Sonnevend, A
Coquet, L
Leprince, J
Jouenne, T
Vaudry, H
Iwamuro, S
机构
[1] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Biochem, Al Ain 17666, U Arab Emirates
[2] United Arab Emirates Univ, Fac Med & Hlth Sci, Dept Med Microbiol, Al Ain 17666, U Arab Emirates
[3] Univ Rouen, CNRS, European Inst Peptide Res, F-76821 Mont St Aignan, France
[4] Univ Rouen, CNRS, UMR 6522, F-76821 Mont St Aignan, France
[5] Univ Rouen, CNRS, U 413, INSERM, F-76821 Mont St Aignan, France
[6] Toho Univ, Fac Sci, Dept Biol, Funabashi, Chiba 2748510, Japan
来源
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY C-TOXICOLOGY & PHARMACOLOGY | 2006年 / 143卷 / 01期
关键词
brevinin-1; brevinin-2; temporin; frog skin; antimicrobial peptide; HPLC purification;
D O I
10.1016/j.cbpc.2005.11.022
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
The Tsushima brown frog Rana tsushimensis Stejneger, 1907 exists in reproductive isolation on the island of Tsushima, Japan. Six peptides with antimicrobial activity were isolated in pure form from an extract of the skin of this species and their amino acid sequences identified them as members of the brevinin-1 (one peptide), brevinin-2 (one peptide) and temporin (four peptides) families. The C-terminally a-amidated brevinin-1 peptide (FLGSIVGALASALPSLISKIRN.NH2) lacks the cyclic heptapeptide domain Cys(18)-(Xaa)(4)-Lys-Cys(24) at the COOH-terminus of the molecule that characterizes other members of that family. A structurally similar brevinin-1 peptide, also lacking the cyclic domain, was previously isolated from the skin of the Ryukyu brown frog Rana okinavana, indicative of a close phylogenetic relationship between the species. Brevinin-2TSa (GIMSLFKGVLKTAGKHVAGSLVDQLKCKITGGC) showed broad-spectrum growth inhibitory activity against a range of Gram-negative and Gram-positive bacteria (including methicillin-resistant Staphylococcus aureus) (minimum inhibitory concentrations <= 25 mu M) and relatively low hemolytic activity against human erythrocytes (LD50=100 mu M). The peptide therefore represents a candidate for drug development. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:42 / 49
页数:8
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