The Mycobacterium tuberculosis membrane protein Rv2560 - Biochemical and functional studies

The characterization of membrane proteins having no identified function in Mycobacterium tuberculosis is important for a better understanding of the biology of this pathogen. In this work, the biological activity of the Rv2560 protein was characterized and evaluated. Primers used in PCR and RT-PCR a...

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Autores:
Tipo de recurso:
Fecha de publicación:
2007
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/24055
Acceso en línea:
https://doi.org/10.1111/j.1742-4658.2007.06153.x
https://repository.urosario.edu.co/handle/10336/24055
Palabra clave:
Membrane protein
Polymer
Rv2560 protein
Unclassified drug
Article
Biochemistry
Biological activity
Controlled study
Cross linking
Epithelium cell
Human
Human cell
Immunoelectron microscopy
Monocyte
Mycobacterium tuberculosis
Nonhuman
Polymerase chain reaction
Priority journal
Rabbit
Reverse transcription polymerase chain reaction
Amino acid sequence
Animals
Bacterial proteins
Circular dichroism
Flow cytometry
Humans
Immune sera
Immunization
Membrane proteins
Molecular sequence data
Mycobacterium tuberculosis
Polymerase chain reaction
Protein binding
Rabbits
U937 cells
Mycobacterium tuberculosis
Oryctolagus cuniculus
High-activity binding peptide
Invasion inhibition
Mycobacterium tuberculosis- host cell interaction
Rv2560 membrane protein
protein
western
tumor
mass
bacterial
dna
immunoelectron
matrix-assisted laser desorption-ionization
Blotting
Cell line
Dna
Microscopy
Sequence analysis
Sequence analysis
Spectrometry
Rights
License
Abierto (Texto Completo)
Description
Summary:The characterization of membrane proteins having no identified function in Mycobacterium tuberculosis is important for a better understanding of the biology of this pathogen. In this work, the biological activity of the Rv2560 protein was characterized and evaluated. Primers used in PCR and RT-PCR assays revealed that the gene encoding protein Rv2560 is present in M. tuberculosis complex strains, but transcribed in only some of them. Sera obtained from rabbits inoculated with polymer peptides from this protein recognized a 33 kDa band in the M. tuberculosis lysate and a membrane fraction corresponding to the predicted molecular mass (33.1 kDa) of this protein. Immunoelectron microscopy analysis found this protein on the mycobacterial membrane. Sixteen peptides covering its entire length were chemically synthesized and tested for their ability to bind to A549 and U937 cells. Peptide 11024 (121VVALSDRATTAYTNTSGVSS140) showed high specific binding to both cell types (dissociation constants of 380 and 800 nm, respectively, and positive receptor-ligand interaction cooperativity), whereas peptide 11033 (284LIGIPVAALIHVYTYRKLSGG304) displayed high binding activity to A549 cells only. Cross-linking assays showed the specific binding of peptide 11024 to a 54 kDa membrane protein on U937. Invasion inhibition assays, in the presence of shared high-activity binding peptide identified for U937 and A549 cells, presented maximum inhibition percentages of 50.53% and 58.27%, respectively. Our work highlights the relevance of the Rv2560 protein in the M. tuberculosis invasion process of monocytes and epithelial cells, and represents a fundamental step in the rational selection of new antigens to be included as components in a multiepitope, subunit-based, chemically synthesized, antituberculosis vaccine. © 2007 The Authors.