Mycobacterium tuberculosis H37Rv ESAT-6-CFP-10 complex formation confers thermodynamic and biochemical stability (Q28239641)

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Naresh Chandra Bal

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Kandala V R Chary

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Ashish Arora

Mutually dependent secretion of proteins required for mycobacterial virulence.

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language of work or name

English

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publication date

April 2006

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published in

FEBS Journal

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volume

273

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issue

7

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page(s)

1445-62

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cites work

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Conclusive evidence that the major T-cell antigens of the Mycobacterium tuberculosis complex ESAT-6 and CFP-10 form a tight, 1:1 complex and characterization of the structural properties of ESAT-6, CFP-10, and the ESAT-6*CFP-10 complex. Implications

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Structure and function of the complex formed by the tuberculosis virulence factors CFP-10 and ESAT-6

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Individual RD1-region genes are required for export of ESAT-6/CFP-10 and for virulence of Mycobacterium tuberculosis

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Isothermal titration calorimetry of protein-protein interactions

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The program XEASY for computer-supported NMR spectral analysis of biological macromolecules

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Comparative genomics of BCG vaccines by whole-genome DNA microarray

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Diagnosis of tuberculosis based on the two specific antigens ESAT-6 and CFP10.

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A mycobacterial virulence gene cluster extending RD1 is required for cytolysis, bacterial spreading and ESAT-6 secretion

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The primary mechanism of attenuation of bacillus Calmette-Guerin is a loss of secreted lytic function required for invasion of lung interstitial tissue

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Isothermal titration calorimetry and differential scanning calorimetry as complementary tools to investigate the energetics of biomolecular recognition

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Green fluorescent protein as a new expression marker in mycobacteria

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Recombinant BCG exporting ESAT-6 confers enhanced protection against tuberculosis

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Down‐Regulation of T Helper 1 Responses to Mycobacterial Antigens Due to Maturation of Dendritic Cells by 10‐kDaMycobacterium tuberculosisSecretory Antigen

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