selleck chemical tuberculosis [16]. Particularly, lipoproteins have been shown to trigger cytokine signaling via toll-like receptors on the surface of mammalian cells and therefore have been considered to be important effectors that may contribute to the pathogen’s virulence. However, only a reduced number of predicted mycobacteriallipoproteins have been experimentally characterized [17]. Our institute has studied ligand-receptor interactions established between synthetic peptides derived from pathogen proteins and host-cell surface receptors,
with the purpose of identifying high activity binding peptides (HABPs) involved in specific host-pathogen recognition interactions, and that could therefore be potential components of subunit vaccines. This methodology has been used and tested on this website different pathogens, including Plasmodium falciparum, Plasmodium vivax [18–20], Human papillomavirus [21] and Epstein-Barr virus [22], among others. Specifically in the case of M. tuberculosis, our group has characterized and determined the binding profiles of three mycobacterial membrane proteins [23–25]. More recently, the biological relevance of HABPs derived from some other mycobacterial proteins has been demonstrated using a flow-cytometry-based assay to assess the capacity of HABPs to mycobacterial inhibit invasion of target cells [26–28]. This study focused on the Rv0679c protein of M. tuberculosis,
AZD6244 cell line which is classified as a hypothetical membrane protein of the cell envelope. Its protein homolog in M. bovis BCG is a putative lipoprotein that has been shown to be tightly associated to lipoarabinomannan (LAM) [29], one of the major components of cell envelope involved in pro-inflammatory and anti-inflammatory responses [30]. The aim of the present study was to identify Rv0679c HABPs capable
of inhibiting M. tuberculosis invasion of target cells that could therefore be considered as potential as candidate components for a chemically synthesized, subunit-based antituberculous vaccine. Methods Bioinformatics analysis The sequence selleckchem of the M. tuberculosis Rv0679c protein was downloaded from Tuberculist http://genolist.pasteur.fr/TubercuList/ and used as query sequence of a BLAST search http://www.ncbi.nlm.nih.gov/BLAST/. Type I and II signal peptides (typical of lipoproteins) were identified using LipoP 1.0 http://www.cbs.dtu.dk/services/LipoP/. Transmembrane regions were predicted using TMHMM v. 2.0 http://www.cbs.dtu.dk/services/TMHMM and TMPRED http://www.ch.embnet.org/software/TMPRED_form.html. Molecular assays The presence and transcription of the Rv0679c gene was assessed in species and strains belonging to the M. tuberculosis complex and in mycobacteria other than tuberculosis. The following strains were tested (26 in total): M. tuberculosis H37Rv (ATCC 27294), M.