Identification of novel bacterial plasminogen-binding proteins in the human pathogen Mycobacterium tuberculosis

• Published in: Proteomics (Weinheim) Vol. 7; no. 18; pp. 3332 - 3341
• Main Authors: Xolalpa, Wendy, Vallecillo, Antonio J., Lara, Martha, Mendoza-Hernandez, Guillermo, Comini, Marcelo, Spallek, Ralf, Singh, Mahavir, Espitia, Clara
• Format: Journal Article
• Language: English
• Published: Weinheim WILEY-VCH Verlag 01-09-2007; WILEY‐VCH Verlag; Wiley-VCH
• Subjects: 2-DE; Amino Acid Sequence; Analytical, structural and metabolic biochemistry; Bacterial Proteins - chemistry; Bacterial Proteins - metabolism; Bacteriology; Base Sequence; Biological and medical sciences; Blotting, Western; Chromatography, Liquid; DNA Primers; Electrophoresis, Polyacrylamide Gel; Enzyme-Linked Immunosorbent Assay; Fundamental and applied biological sciences. Psychology; Ligand blotting; Ligands; Microbiology; Miscellaneous; Mycobacterium tuberculosis; Mycobacterium tuberculosis - metabolism; Plasminogen - metabolism; Plasminogen receptors; Proteins; Spectrometry, Mass, Electrospray Ionization; Human; Plasminogen receptors; Identification; 2-DE; Ligand blotting; Infection; Binding protein; Mycobacterium tuberculosis; Mycobacteriales; Proteomics; Mycobacteriaceae; Bacteriosis; Bacteria; Actinomycetes; Plasminogen
• ISSN: 1615-9853; 1615-9861
• DOI: 10.1002/pmic.200600876

Binding and activation of human plasminogen (Plg) to generate the proteolytic enzyme plasmin (Plm) have been associated with the invasive potential of certain bacteria. In this work, proteomic analysis together with ligand blotting assays identified several major Plg‐binding spots in Mycobacterium tuberculosis soluble extracts (SEs) and culture filtrate proteins. The identity of 15 different proteins was deduced by N‐terminal and/or MS and corresponded to DnaK, GroES, GlnA1, Ag85 complex, Mpt51, Mpt64, PrcB, MetK, SahH, Lpd, Icl, Fba, and EF‐Tu. Binding of Plg to recombinant M. tuberculosis DnaK, GlnA1, and Ag85B was further confirmed by ELISA and ligand blotting assays. The binding was inhibited by ϵ‐aminocaproic acid, indicating that the interaction involved lysine residues. Plg bound to recombinant mycobacterial proteins was activated to Plm by tissue‐type Plg activator. In contrast with recombinant proteins, M. tuberculosis SE enhanced several times the Plg activation mediated by the activator. Interestingly, GlnA1 was able to bind the extracellular matrix (ECM) protein fibronectin. Together these results show that M. tuberculosis posses several Plg receptors suggesting that bound Plg to bacteria surface, can be activated to Plm, endowing bacteria with the ability to break down ECM and basal membranes proteins contributing to tissue injury in tuberculosis.