Javidlab: Difference between revisions

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1. 'Adaptive mistranslation'<br>
1. 'Adaptive mistranslation'<br>
2. Mycobacteria and host-pathogen interactions<br>
2. Mycobacteria and host-pathogen interactions<br>
3. Protein translation fidelity in mycobacteria<br>
3. Protein translation fidelity in mycobacteria<br>
4. GatCAB dependent tRNA synthesis and protein evolution<br>
4. GatCAB dependent tRNA synthesis and protein evolution<br>
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INTEREST<br>
INTEREST<br>
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The Javid lab principal interest is in mycobacterial pathophysiology. Tuberculosis causes more infectious disease deaths in China than any other pathogen, and the basic biology of its causative organism,Mycobacterium tuberculosis is still poorly understood.Our lab is interested in how fundamental physiological processes in mycobacteria can influence important clinical phenotypes such as antibiotic tolerance and immune evasion. We have shown that altering the protein translation error rate in mycobacteria can profoundly influence phenotypic resistance to first-line anti-mycobacterial drugs. We are now trying to understand the molecular mechanism and regulation of translational fidelity.Mycobacterium tuberculosis can reside within the host for decades without detection. We are trying to understand how this happens -- at the level of both innate and adaptive immunity.
The Javid lab principal interest is in mycobacterial pathophysiology. Tuberculosis causes more infectious disease deaths in China than any other pathogen, and the basic biology of its causative organism,Mycobacterium tuberculosis is still poorly understood.Our lab is interested in how fundamental physiological processes in mycobacteria can influence important clinical phenotypes such as antibiotic tolerance and immune evasion. We have shown that altering the protein translation error rate in mycobacteria can profoundly influence phenotypic resistance to first-line anti-mycobacterial drugs. We are now trying to understand the molecular mechanism and regulation of translational fidelity.Mycobacterium tuberculosis can reside within the host for decades without detection. We are trying to understand how this happens -- at the level of both innate and adaptive immunity.
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Revision as of 04:35, 23 May 2013



MAIN
TOPIC



1. 'Adaptive mistranslation'
2. Mycobacteria and host-pathogen interactions
3. Protein translation fidelity in mycobacteria
4. GatCAB dependent tRNA synthesis and protein evolution


RESEARCH
INTEREST



The Javid lab principal interest is in mycobacterial pathophysiology. Tuberculosis causes more infectious disease deaths in China than any other pathogen, and the basic biology of its causative organism,Mycobacterium tuberculosis is still poorly understood.Our lab is interested in how fundamental physiological processes in mycobacteria can influence important clinical phenotypes such as antibiotic tolerance and immune evasion. We have shown that altering the protein translation error rate in mycobacteria can profoundly influence phenotypic resistance to first-line anti-mycobacterial drugs. We are now trying to understand the molecular mechanism and regulation of translational fidelity.Mycobacterium tuberculosis can reside within the host for decades without detection. We are trying to understand how this happens -- at the level of both innate and adaptive immunity.


>>>>>>>>>>>
See our members in the LINK below

LINK:
Javidlab:labmembers


Amaze yourself by seeing the LINK below

LINK:
Javidlab:research




Lab name written by Nano Luciferase

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Nano Luciferase

Bio_luminescence by Nano Luciferase (Promega), which we optimised to be easily expressed in Mycobacterium, and a novel mistranslation reporter with 100 times higher signal over canonical Renilla luciferase.