نتایج جستجو برای: furin

تعداد نتایج: 1326  

Journal: :Journal of virology 1999
R J Wool-Lewis P Bates

Proteolytic processing is required for the activation of numerous viral glycoproteins. Here we show that the envelope glycoprotein from the Zaire strain of Ebola virus (Ebo-GP) is proteolytically processed into two subunits, GP1 and GP2, that are likely covalently associated through a disulfide linkage. Murine leukemia virions pseudotyped with Ebo-GP contain almost exclusively processed glycopr...

Journal: :Physiological research 2010
J Krijt Y Fujikura L Sefc M Vokurka T Hlobenová E Necas

Hepcidin is a key regulator of iron homeostasis, while hemojuvelin is an important component of the hepcidin regulation pathway. It has been recently proposed that soluble hemojuvelin, produced from hemojuvelin by the protease furin, decreases hepcidin expression. The aim of the presented study was to examine the downregulation of hepcidin by chronic bleeding in hemojuvelin-mutant mice. Male mi...

Journal: :The Journal of clinical investigation 2008
Nathalie Scamuffa Geraldine Siegfried Yannick Bontemps Liming Ma Ajoy Basak Ghislaine Cherel Fabien Calvo Nabil G Seidah Abdel-Majid Khatib

The proprotein convertases (PCs) are implicated in the activation of various precursor proteins that play an important role in tumor cell metastasis. Here, we report their involvement in the regulation of the metastatic potential of colorectal tumor cells. PC function in the human and murine colon carcinoma cell lines HT-29 and CT-26, respectively, was inhibited using siRNA targeting the PCs fu...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1994
M Zheng R D Streck R E Scott N G Seidah J E Pintar

The genes encoding mammalian subtilisin-like endoproteases furin, PC1, and PC2 have been isolated and are implicated in endoproteolytic cleavage of precursor molecules, which is a key step in posttranslational maturation of proproteins and neuropeptide precursors. Following endoproteolytic cleavage, the carboxyl-terminal basic amino acid residues are removed by carboxypeptidase E (CPE). We have...

Journal: :Mechanisms of Development 2002
Simon Kidd Toby Lieber

Notch (N) is a large transmembrane protein that acts as a receptor in an evolutionarily conserved intercellular signalling pathway. Because of this conservation, it has been assumed that biochemical events mediating N function are identical in all species. For instance, intracellular maturation by furin protease and subunit assembly leading to the formation of a heterodimeric cell surface N rec...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
V E Volchkov H Feldmann V A Volchkova H D Klenk

In the present study, we have investigated processing and maturation of the envelope glycoprotein (GP) of Ebola virus. When GP expressed from vaccinia virus vectors was analyzed by pulse-chase experiments, the mature form and two different precursors were identified. First, the endoplasmic reticulum form preGPer, full-length GP with oligomannosidic N-glycans, was detected. preGPer (110 kDa) was...

Journal: :The Biochemical journal 2003
Sara A Illman Jorma Keski-Oja William C Parks Jouko Lohi

Epilysin (MMP-28) is a recently identified member of the matrix metalloproteinase (MMP) family. To explore the expression of epilysin in vivo and to gain insight into its biological functions, we have cloned the mouse epilysin cDNA and determined its expression. The amino acid sequence of the mouse protein is 85% identical with the human sequence and contains conserved features such as an RKKR ...

Journal: :The Biochemical journal 2001
A Basak M Zhong J S Munzer M Chrétien N G Seidah

Fluorogenic peptides encompassing the processing sites of envelope glycoproteins of the infectious influenza A Hong Kong virus (HKV), Ebola virus (EBOV) and respiratory syncytial virus (RSV) were tested for cleavage by soluble recombinants of the proprotein convertases furin, PC5 and PC7. Kinetic studies with these intramolecularly quenched fluorogenic peptides revealed selective cleavages at t...

Journal: :Journal of cell science 1999
M Raghunath E A Putnam T Ritty D Hamstra E S Park M Tschödrich-Rotter R Peters A Rehemtulla D M Milewicz

Fibrillin-1, the main component of 10-12 nm microfibrils of the extracellular matrix, is synthesized as profibrillin and proteolytically processed to fibrillin. The putative cleavage site has been mapped to the carboxy-terminal domain of profibrillin-1, between amino acids arginine 2731 and serine 2732, by a spontaneous mutation in this recognition site that prevents profibrillin conversion. Th...

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