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Submitted on June 30, 2003
Bioscience Dept., Los Alamos National Lab, Los Alamos, NM 87545
Corresponding Author: chen_xian{at}lanl.gov
Mycobacterium tuberculosis (MTB) is an infectious microorganism that causes human tuberculosis. The cell membrane of a pathogen is known to be rich in diagnostic and therapeutic protein targets. To compliment the MTB genome, we have profiled the membrane protein fraction of the M. tuberculosis H37Rv strain using an analytical platform that couples 1D SDS gels to a microcapillary liquid chromatography-nanospray-tandem mass spectrometer. As a result, 739 proteins has been identified by 2 or more distinct peptide sequences and characterized. Interestingly, approximately 450 proteins represent novel identifications, 79 of which are membrane proteins and more than a hundred are membrane-associated proteins. The physicochemical properties of the identified proteins were studied in detail and then biological functions were obtained by sorting them according Sanger Institute gene function category. Many membrane proteins were found to be involved in the cell envelope and those proteins with energy metabolic functions were also identified in this study
Revised on October 3, 2003
Accepted on October 6, 2003
Comprehensive proteomic profiling of the membrane constituents of A mycobacterium tuberculosis strain
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