Literature DB >> 8561461

Peptides as weapons against microorganisms in the chemical defense system of vertebrates.

P Nicolas1, A Mor.   

Abstract

The innate immunity of vertebrates to microbial invasion is arbitrated by a network of host-defense mechanisms involving both the long-lasting highly specific responses of the cell-mediated immune system and a nonspecific chemical defense system based on a series of broad-spectrum antimicrobial peptides that are analogous to those found in insects. Vertebrate antibiotic peptides secreted by nonlymphoid cells of the mucosal surfaces of the respiratory and gastrointestinal tracts as well as by the granular glands of the skin reportedly cause the lysis of numerous pathogenic microorganisms, including viruses, gram-positive and gram-negative bacteria, protozoa, yeasts, and fungi, as well as of cancer cells. Antimicrobial peptides isolated from vertebrates have three characteristic properties: They are relatively small (20-46 amino acid residues), basic (lysine- or arginine-rich), and amphipathic. Although these peptides differ widely in length and amino acid sequences, they may be grouped in four broad families based on characteristic structural features. Although the precise mechanism of action of these peptides remains to be defined, their microbicidal effect very likely results from their capacity to form channels or pores within the microbial membrane in order to permeate the cell and impair its ability to carry out anabolic processes. This secondary, chemical immune system provides vertebrates with a repertoire of small peptides that are promptly synthesized upon induction, easily stored in large amounts, and readily available for antimicrobial warfare.

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Year:  1995        PMID: 8561461     DOI: 10.1146/annurev.mi.49.100195.001425

Source DB:  PubMed          Journal:  Annu Rev Microbiol        ISSN: 0066-4227            Impact factor:   15.500


  98 in total

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Authors:  L A Rollins-Smith
Journal:  Immunol Res       Date:  2001       Impact factor: 2.829

2.  Antimalarial activities of dermaseptin S4 derivatives.

Authors:  M Krugliak; R Feder; V Y Zolotarev; L Gaidukov; A Dagan; H Ginsburg; A Mor
Journal:  Antimicrob Agents Chemother       Date:  2000-09       Impact factor: 5.191

3.  Energetics and self-assembly of amphipathic peptide pores in lipid membranes.

Authors:  Assaf Zemel; Deborah R Fattal; Avinoam Ben-Shaul
Journal:  Biophys J       Date:  2003-04       Impact factor: 4.033

4.  Activities of temporin family peptides against the chytrid fungus (Batrachochytrium dendrobatidis) associated with global amphibian declines.

Authors:  Louise A Rollins-Smith; Cynthia Carey; J Michael Conlon; Laura K Reinert; Jennifer K Doersam; Tomas Bergman; Jerzy Silberring; Hilkka Lankinen; David Wade
Journal:  Antimicrob Agents Chemother       Date:  2003-03       Impact factor: 5.191

5.  Membrane perturbation induced by interfacially adsorbed peptides.

Authors:  Assaf Zemel; Avinoam Ben-Shaul; Sylvio May
Journal:  Biophys J       Date:  2004-06       Impact factor: 4.033

6.  In vitro activity and potency of an intravenously injected antimicrobial peptide and its DL amino acid analog in mice infected with bacteria.

Authors:  Amir Braunstein; Niv Papo; Yechiel Shai
Journal:  Antimicrob Agents Chemother       Date:  2004-08       Impact factor: 5.191

Review 7.  Nonmammalian vertebrate antibiotic peptides.

Authors:  P Síma; I Trebichavský; K Sigler
Journal:  Folia Microbiol (Praha)       Date:  2003       Impact factor: 2.099

8.  Complete amino acid sequence of globin chains and biological activity of fragmented crocodile hemoglobin (Crocodylus siamensis).

Authors:  Saowaluck Srihongthong; Anawat Pakdeesuwan; Sakda Daduang; Tomohiro Araki; Apisak Dhiravisit; Sompong Thammasirirak
Journal:  Protein J       Date:  2012-08       Impact factor: 2.371

9.  Protegrin-1: a broad-spectrum, rapidly microbicidal peptide with in vivo activity.

Authors:  D A Steinberg; M A Hurst; C A Fujii; A H Kung; J F Ho; F C Cheng; D J Loury; J C Fiddes
Journal:  Antimicrob Agents Chemother       Date:  1997-08       Impact factor: 5.191

10.  Role of proline, cysteine and a disulphide bridge in the structure and activity of the anti-microbial peptide gaegurin 5.

Authors:  Sang-Ho Park; Hyung-Eun Kim; Chi-Man Kim; Hee-Jeong Yun; Eung-Chil Choi; Bong-Jin Lee
Journal:  Biochem J       Date:  2002-11-15       Impact factor: 3.857

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