Quantitative proteomic analysis of drug-induced changes in mycobacteria

被引:63
作者
Hughes, MA
Silva, JC
Geromanos, SJ
Townsend, CA
机构
[1] Johns Hopkins Univ, Dept Chem, Baltimore, MD 21218 USA
[2] Waters Corp, Milford, MA 01757 USA
关键词
isoniazid; tuberculosis; protein profiling; liquid chromatography; mass spectrometry;
D O I
10.1021/pr050248t
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A new approach for qualitative and quantitative proteomic analysis using capillary liquid chromatography and mass spectrometry to study the protein expression response in mycobacteria following isoniazid treatment is discussed. In keeping with known effects on the fatty acid synthase II pathway, proteins encoded by the kas operon (AcpM, KasA, KasB, Accd6) were significantly overexpressed, as were those involved in iron metabolism and cell division suggesting a complex interplay of metabolic events leading to cell death.
引用
收藏
页码:54 / 63
页数:10
相关论文
共 45 条
  • [1] Identification of differentially expressed mRNA in prokaryotic organisms by customized amplification libraries (DECAL):: The effect of isoniazid on gene expression in Mycobacterium tuberculosis
    Alland, D
    Kramnik, I
    Weisbrod, TR
    Otsubo, L
    Cerny, R
    Miller, LP
    Jacobs, WR
    Bloom, BR
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) : 13227 - 13232
  • [2] The influence of reduced oxygen availability on pathogenicity and gene expression in Mycobacterium tuberculosis
    Bacon, J
    James, BW
    Wernisch, L
    Williams, A
    Morley, KA
    Hatch, GJ
    Mangan, JA
    Hinds, J
    Stoker, NG
    Butcher, PD
    Marsh, PD
    [J]. TUBERCULOSIS, 2004, 84 (3-4) : 205 - 217
  • [3] Effects of isoniazid on ultrastructure of Mycobacterium aurum and Mycobacterium tuberculosis and on production of secreted proteins
    Bardou, F
    Quemard, A
    Dupont, MA
    Horn, C
    Marchal, G
    Daffe, M
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (11) : 2459 - 2467
  • [4] BATEMAN RH, 2002, Patent No. 2364168A
  • [5] Bentrup KHZ, 1999, J BACTERIOL, V181, P7161
  • [6] INHIBITION OF LIPID BIOSYNTHESIS INDUCES THE EXPRESSION OF THE PSPA GENE
    BERGLER, H
    ABRAHAM, D
    ASCHAUER, H
    TURNOWSKY, F
    [J]. MICROBIOLOGY-SGM, 1994, 140 : 1937 - 1944
  • [7] Evaluation of a nutrient starvation model of Mycobacterium tuberculosis persistence by gene and protein expression profiling
    Betts, JC
    Lukey, PT
    Robb, LC
    McAdam, RA
    Duncan, K
    [J]. MOLECULAR MICROBIOLOGY, 2002, 43 (03) : 717 - 731
  • [8] Signature gene expression profiles discriminate between isoniazid-, thiolactomycin-, and triclosan-treated Mycobacterium tuberculosis
    Betts, JC
    McLaren, A
    Lennon, MG
    Kelly, FM
    Lukey, PT
    Blakemore, SJ
    Duncan, K
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (09) : 2903 - 2913
  • [9] NATIONWIDE SURVEY OF DRUG-RESISTANT TUBERCULOSIS IN THE UNITED-STATES
    BLOCH, AB
    CAUTHEN, GM
    ONORATO, IM
    DANSBURY, KG
    KELLY, GD
    DRIVER, CR
    SNIDER, DE
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1994, 271 (09): : 665 - 671
  • [10] The transcriptional responses of Mycobacterium tuberculosis to inhibitors of metabolism -: Novel insights into drug mechanisms of action
    Boshoff, HIM
    Myers, TG
    Copp, BR
    McNeil, MR
    Wilson, MA
    Barry, CE
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (38) : 40174 - 40184