نتایج جستجو برای: hspx/ esxs fusion protein

تعداد نتایج: 1323442  

Arshid Yousefi-Avarvand, Ehsan Aryan, Farzad Khademi, Kiarash Ghazvini, Mohammad Derakhshan, Mohsen Tafaghodi, Mojtaba Sankian, Zahra Meshkat,

Background: The purpose of this study was to clone, express, and purify a novel multidomain fusion protein of Micobacterium tuberculosis (Mtb) in a prokaryotic system. Methods: An hspX/esxS gene construct was synthesized and ligated into a pGH plasmid, E. coli TOP10 cells were transformed, and the vector was purified. The vector containing the construct and pET-21b (+) plasmid were digested ...

Journal: :reports of biochemistry and molecular biology 0
farzad khademi antimicrobial resistance research center, department of medical bacteriology and virology, qaem university hospital, school of medicine, mashhad university of medical sciences, mashhad, iran. arshid yousefi-avarvand antimicrobial resistance research center, department of medical bacteriology and virology, qaem university hospital, school of medicine, mashhad university of medical sciences, mashhad, iran. mohammad derakhshan antimicrobial resistance research center, department of medical bacteriology and virology, qaem university hospital, school of medicine, mashhad university of medical sciences, mashhad, iran. zahra meshkat antimicrobial resistance research center, department of medical bacteriology and virology, qaem university hospital, school of medicine, mashhad university of medical sciences, mashhad, iran. mohsen tafaghodi nanotechnology research center, school of pharmacy, mashhad university of medical sciences, mashhad, iran. kiarash ghazvini antimicrobial resistance research center, department of medical bacteriology and virology, qaem university hospital, school of medicine, mashhad university of medical sciences, mashhad, iran.

background: the purpose of this study was to clone, express, and purify a novel multidomain fusion protein of micobacterium tuberculosis (mtb) in a prokaryotic system. methods: an hspx/esxs gene construct was synthesized and ligated into a pgh plasmid, e. coli top10 cells were transformed, and the vector was purified. the vector containing the construct and pet-21b (+) plasmid were digested wit...

Journal: :Reports of biochemistry & molecular biology 2017
Farzad Khademi Arshid Yousefi-Avarvand Mohammad Derakhshan Zahra Meshkat Mohsen Tafaghodi Kiarash Ghazvini Ehsan Aryan Mojtaba Sankian

BACKGROUND The purpose of this study was to clone, express, and purify a novel multidomain fusion protein of Micobacterium tuberculosis (Mtb) in a prokaryotic system. METHODS An hspX/esxS gene construct was synthesized and ligated into a pGH plasmid, E. coli TOP10 cells were transformed, and the vector was purified. The vector containing the construct and pET-21b (+) plasmid were digested wit...

Objective(s): A new strategy in recent studies is using effective tuberculosis (TB) subunit vaccines combined with appropriate carriers and adjuvants which have shown promising results in preclinical and clinical studies. The aim of the present study was to evaluate the PLGA:DDA hybrid nanoparticles (NPs) for subcutaneous delivery of a novel multistage subunit vaccine ...

Polymeric particles and liposomes are efficient tools to overcome the low immunogenicity of subunit vaccines. The aim of the present study was formulation and optimization of a new cationic lipid-modified PLGA nanoparticles (NPs) as a delivery system for Mycobacterium tuberculosis HspX/EsxS fusion protein. The cationic lipid-modified PLGA NPs containing HspX/EsxS fusion protein were prepared us...

Polymeric particles and liposomes are efficient tools to overcome the low immunogenicity of subunit vaccines. The aim of the present study was formulation and optimization of a new cationic lipid-modified PLGA nanoparticles (NPs) as a delivery system for Mycobacterium tuberculosis HspX/EsxS fusion protein. The cationic lipid-modified PLGA NPs containing HspX/EsxS fusion protein were prepared us...

2016
Ruqyya Khalid Madeeha Afzal Sana Khurshid Rehan Zafar Paracha Imran H Khan Muhammad Waheed Akhtar

Variable individual response against the antigens of Mycobacterium tuberculosis necessitates detection of multiple antibodies for enhancing reliability of serodiagnosis of tuberculosis. Fusion molecules consisting of two or more antigens showing high sensitivity would be helpful in achieving this objective. Antigens of M. tuberculosis HSPX and PE35 were expressed in a soluble form whereas tnPst...

Background: Subunit vaccines are appropriate vaccine candidates for the prevention of some infections. In this study, three immunogenic proteins of Mycobacterium tuberculosis, including HspX, Ppe44, and EsxV as a new construction, were expressed alone and as a fusion protein to develop a new vaccine candidate against tuberculosis infection. Methods: To make the fusion protein, the three genes ...

Journal: :reports of biochemistry and molecular biology 0
bagher moradi antimicrobial resistance research center, mashhad university of medical sciences, mashhad, iran mojtaba sankian immunology research center, mashhad university of medical sciences, mashhad, iran. yousef amini immunology research center, mashhad university of medical sciences, mashhad, iran. zahra meshkat tel: +985138012453; fax: +98-5118409612

background: mycobacterium tuberculosis is the causative agent of tuberculosis (tb). bacille calmette-guerin (bcg) vaccine, is not effective in adults, therefore, many efforts have been made to produce an effective adult tb vaccine. the aim of this study was to develop a new tuberculosis dna vaccine candidate encoding a recombinant hspx-ppe44-esxv fusion antigen of m. tuberculosis. methods: a fu...

Bagher Moradi, Mojtaba Sankian, Yousef Amini, Zahra Meshkat,

Background: Mycobacterium tuberculosis is the causative agent of tuberculosis (TB). Bacille Calmette-Guerin (BCG) vaccine, is not effective in adults, therefore, many efforts have been made to produce an effective adult TB vaccine. The aim of this study was to develop a new tuberculosis DNA vaccine candidate encoding a recombinant HspX-PPE44-EsxV fusion antigen of M. tuberculosis. Methods: ...

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