نتایج جستجو برای: protein refolding

تعداد نتایج: 1235541  

2007
Anwer Mujeeb Nikolai B. Ulyanov Stefanos Georgantis Ivan Smirnov Janet Chung Tristram G. Parslow Thomas L. James

Specific binding of HIV-1 viral protein NCp7 to a unique 35-base RNA stem-loop SL1 is critical for formation and packaging of the genomic RNA dimer found within HIV-1 virions. NCp7 binding stimulates refolding of SL1 from a metastable kissing dimer (KD) into thermodynamically stable linear dimer (LD). Using UV melting, gel electrophoresis and heteronuclear NMR, we investigated effects of variou...

Malihe Moghadam, Maryam Ghodsi, Merat Mahmoodi, Mojtaba Sankian,

Background: The expression of mouse tumor necrosis factor alpha (TNF-α) in Escherichia coli is a favorable way to get high yield of protein; however, the formation of cytoplasmic inclusion bodies, which is the consequence of insoluble accumulated proteins, is a major obstacle in this system. To overcome this obstacle, we used a pulsed dilution method to convert the product to its native c...

Journal: :BMC Biotechnology 2009
Xiao-Tao Wang Paul C Engel

BACKGROUND Human glucose 6-phosphate dehydrogenase (G6PD), active in both dimer and tetramer forms, is the key entry enzyme in the pentose phosphate pathway (PPP), providing NADPH for biosynthesis and various other purposes, including protection against oxidative stress in erythrocytes. Accordingly haemolytic disease is a major consequence of G6PD deficiency mutations in man, and many severe di...

2005
Laura Lin Jasbir Seehra Mark L. Stahl

The expression of human genes in bacteria is often one of the most eYcient systems for generating proteins for drug discovery eVorts. However, expression of mammalian cDNAs in Escherichia coli often results in the production of protein that is insoluble and misfolded and thus requires the development of a successful refolding procedure to generate active protein. To accelerate the process of de...

2014
Hiroshi Yamaguchi Masaya Miyazaki

Biologically active proteins are useful for studying the biological functions of genes and for the development of therapeutic drugs and biomaterials in a biotechnology industry. Overexpression of recombinant proteins in bacteria, such as Escherichia coli, often results in the formation of inclusion bodies, which are protein aggregates with non-native conformations. As inclusion bodies contain r...

Journal: :PloS one 2016
Natalie Di Bartolo Emma L R Compton Tony Warne Patricia C Edwards Christopher G Tate Gebhard F X Schertler Paula J Booth

The factors defining the correct folding and stability of integral membrane proteins are poorly understood. Folding of only a few select membrane proteins has been scrutinised, leaving considerable deficiencies in knowledge for large protein families, such as G protein coupled receptors (GPCRs). Complete reversible folding, which is problematic for any membrane protein, has eluded this dominant...

Journal: :reports of biochemistry and molecular biology 0
mojtaba sankian tel: +98 51 37112610; fax: +98 51 37112596 merat mahmoodi immuno-biochemistry lab, immunology research center, mashhad university of medical sciences, mashhad, iran. maryam ghodsi immuno-biochemistry lab, immunology research center, mashhad university of medical sciences, mashhad, iran. malihe moghadam immuno-biochemistry lab, immunology research center, mashhad university of medical sciences, mashhad, iran.

background: the expression of mouse tumor necrosis factor alpha (tnf-α) in escherichia coli is a favorable way to get high yield of protein; however, the formation of cytoplasmic inclusion bodies, which is the consequence of insoluble accumulated proteins, is a major obstacle in this system. to overcome this obstacle, we used a pulsed dilution method to convert the product to its native conform...

2012
Christy A. Thomson Melanie Olson Linda M. Jackson John W. Schrader

Human granulocyte macrophage colony-stimulating factor (hGM-CSF) is a haematopoietic growth factor and proinflammatory cytokine. Recombinant hGM-CSF is important not only as a research tool but also as a biotherapeutic. However, rhGM-CSF expressed in E. coli is known to form inclusion bodies of misfolded, aggregated protein. Refolding and subsequent purification of rhGM-CSF from inclusion bodie...

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