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Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis

Includes bibliographical references.

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Bibliographic Details
Main Author: Peters, Julian S
Other Authors: Blackburn, Jonathan
Format: Thesis
Language:English
Published: Department of Clinical Laboratory Sciences 2015
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access_status_str Open Access
author Peters, Julian S
author2 Blackburn, Jonathan
author_browse Blackburn, Jonathan
Peters, Julian S
author_facet Blackburn, Jonathan
Peters, Julian S
author_sort Peters, Julian S
collection Thesis
description Includes bibliographical references.
format Thesis
id oai:open.uct.ac.za:11427/12959
institution University of Cape Town (South Africa)
language eng
last_indexed 2026-06-10T12:32:51.499Z
license_str Not specified — see source repository
provenance_str_mv Harvested via OAI-PMH from UCTD — University of Cape Town Open Access Repository
publishDate 2015
publishDateRange 2015
publishDateSort 2015
publisher Department of Clinical Laboratory Sciences
publisherStr Department of Clinical Laboratory Sciences
record_format dspace
source_str UCTD — University of Cape Town Open Access Repository
spelling oai:open.uct.ac.za:11427/12959 Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis Peters, Julian S Blackburn, Jonathan Medical Biochemistry Includes bibliographical references. Tuberculosis is an airborne infectious disease caused by the bacillus known as Mycobacterium tuberculosis. Despite limited genetic variability, Mycobacterium tuberculosis strains exhibit vast discrepancies in phenotypic presentation in terms of virulence, elicited immune response and transmissibility. This study aims to use Mass Spectrometry (MS) tools to quantitatively and qualitatively investigate the total proteome expressed by various epidemiologically significant strains within the Mycobacterium tuberculosis complex (MTBC) as well as a clinically relevant non-tuberculous Mycobacteria (NTM) strain when cultured in vitro. We aim to use the experimental data obtained using discovery mass spectrometry to identify candidate proteins to use in the design of multiple reaction monitoring (MRM) MS experiments for targeted biomarker validation in patient derived biological samples such as sputum. Liquid chromatography mass spectrometry (LC MS/MS) and data capture were carried out using the LTQ Orbitrap Velos. 1D LC was carried out on gel fractionated samples to increase proteome coverage. This allowed a significant increase in the number of protein identifications of up to 80% proteome coverage per strain. Comparative analysis of the datasets was carried out to identify and define the core-proteome expressed across all strains as well as to identify differentially expressed proteins amongst the strains. 2015-05-28T04:14:52Z 2015-05-28T04:14:52Z 2014 Doctoral Thesis Doctoral PhD http://hdl.handle.net/11427/12959 eng application/pdf Department of Clinical Laboratory Sciences Faculty of Health Sciences University of Cape Town
spellingShingle Medical Biochemistry
Peters, Julian S
Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
thesis_degree_str Doctoral
title Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
title_full Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
title_fullStr Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
title_full_unstemmed Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
title_short Comprehensive proteomic profiling of clinically relevant strains of Mycobacterium tuberculosis
title_sort comprehensive proteomic profiling of clinically relevant strains of mycobacterium tuberculosis
topic Medical Biochemistry
url http://hdl.handle.net/11427/12959
work_keys_str_mv AT petersjulians comprehensiveproteomicprofilingofclinicallyrelevantstrainsofmycobacteriumtuberculosis