Structure and Mode of Action of Microplusin, a Copper II-chelating Antimicrobial Peptide from the Cattle Tick Rhipicephalus (Boophilus) microplus


Autoria(s): SILVA, Fernanda D.; REZENDE, Carlos A.; ROSSI, Diego C. P.; ESTEVES, Eliane; DYSZY, Fabio H.; Schreier, Shirley; Filho, Frederico José Gueiros; CAMPOS, Claudia B.; PIRES, Jose R.; DAFFRE, Sirlei
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Microplusin, a Rhipicephalus (Boophilus) microplus antimicrobial peptide (AMP) is the first fully characterized member of a new family of cysteine-rich AMPs with histidine-rich regions at the N and C termini. In the tick, microplusin belongs to the arsenal of innate defense molecules active against bacteria and fungi. Here we describe the NMR solution structure of microplusin and demonstrate that the protein binds copper II and iron II. Structured as a single alpha-helical globular domain, microplusin consists of five alpha-helices: alpha 1 (residues Gly-9 to Arg-21), alpha 2 (residues Glu-27 to Asn-40), alpha 3 (residues Arg-44 to Thr-54), alpha 4 (residues Leu-57 to Tyr-64), and alpha 5 (residues Asn-67 to Cys-80). The N and C termini are disordered. This structure is unlike any other AMP structures described to date. We also used NMR spectroscopy to map the copper binding region on microplusin. Finally, using the Gram-positive bacteria Micrococcus luteus as a model, we studied of mode of action of microplusin. Microplusin has a bacteriostatic effect and does not permeabilize the bacterial membrane. Because microplusin binds metals, we tested whether this was related to its antimicrobial activity. We found that the bacteriostatic effect of microplusin was fully reversed by supplementation of culture media with copper II but not iron II. We also demonstrated that microplusin affects M. luteus respiration, a copper-dependent process. Thus, we conclude that the antibacterial effect of microplusin is due to its ability to bind and sequester copper II.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo, Brazil

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ)

Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro (FAPERJ)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico, Brazil

Identificador

JOURNAL OF BIOLOGICAL CHEMISTRY, v.284, n.50, p.34735-34746, 2009

0021-9258

http://producao.usp.br/handle/BDPI/28514

10.1074/jbc.M109.016410

http://dx.doi.org/10.1074/jbc.M109.016410

Idioma(s)

eng

Publicador

AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Relação

Journal of Biological Chemistry

Direitos

closedAccess

Copyright AMER SOC BIOCHEMISTRY MOLECULAR BIOLOGY INC

Palavras-Chave #PASTEURELLA-HAEMOLYTICA #PSEUDOMONAS-AERUGINOSA #BINDING PROPERTIES #BACILLUS-SUBTILIS #HUMAN LACTOFERRIN #PROTEIN #HEPCIDIN #GOMESIN #MICROORGANISMS #IDENTIFICATION #Biochemistry & Molecular Biology
Tipo

article

original article

publishedVersion