نتایج جستجو برای: furin

تعداد نتایج: 1326  

2013
Chun-Yan Cao Ying-Ying Shen Jian-Dong Wang Li Li Gao-Lin Liang

Herein we developed a new "smart" Gd-based MR contrast agent (i.e., 1) which is susceptive to furin, a protease overexpressed in tumor. Under the action of furin, 1 condenses to form dimers (1-Ds) and the latter self-assemble into gadolinium nanparticles (Gd-NPs). Relaxivity of 1-D is more than 2 folds of those of 1 and magnevist at 1.5 T, and 1.4 folds of that of 1 at 3 T. Intracellular conden...

Journal: :The Biochemical journal 2001
B Plaimauer G Mohr W Wernhart M Himmelspach F Dorner U Schlokat

The human endoprotease furin is involved in the proteolytic maturation of the precursor molecules of a wide variety of bioactive proteins. Despite its localization in the membranes of the trans-Golgi system by means of a transmembrane domain, it has repeatedly been reported to form a C-terminally truncated, naturally secreted form referred to as 'shed' furin. In order to identify the cleavage s...

2014
Sitaram Harihar Keke M. Pounds Tomoo Iwakuma Nabil G. Seidah Danny R. Welch

KISS1 is a broadly functional secreted proprotein that is then processed into small peptides, termed kisspeptins (KP). Since sequence analysis showed cleavage at KR or RR dibasic sites of the nascent protein, it was hypothesized that enzyme(s) belonging to the proprotein convertase family of proteases process KISS1 to generate KP. To this end, cell lines over-expressing KISS1 were treated with ...

Journal: :The Journal of clinical investigation 2003
Geraldine Siegfried Ajoy Basak James A Cromlish Suzanne Benjannet Jadwiga Marcinkiewicz Michel Chrétien Nabil G Seidah Abdel-Majid Khatib

The secretory factor VEGF-C has been directly implicated in various physiological processes during embryogenesis and human cancers. However, the importance of the conversion of its precursor proVEGF-C to mature VEGF-C in tumorigenesis, and vessel formation and the identity of the protease(s) that regulate these processes is/are not known. The intracellular processing of proVEGF-C that occurs wi...

2017
G. N. Nguyen L. A. George J. I. Siner R. J. Davidson C. B. Zander X. L. Zheng V. R. Arruda R. M. Camire D. E. Sabatino

Essentials Factor (F) VIII is an inefficiently expressed protein. Furin deletion FVIII variants were purified and characterized using in vitro and in vivo assays. These minimally modified novel FVIII variants have enhanced function. These variants provide a strategy for increasing FVIII expression in hemophilia A gene therapy. SUMMARY Background The major challenge for developing gene-based t...

Journal: :European heart journal 2014
Tomoko Ichiki John C Burnett

With the discovery that the heart is an endocrine organ, we now know that the heart produces and releases hormones, including the natriuretic peptides (NPs). NPs are thought to be produced and released mainly in response to mechanical stretching, due to increased intravascular volume or under pathophysiological conditions, especially in heart failure (HF). B-type NP (BNP) molecular forms, espec...

2016
Ruud H. P. Wilbers Lotte B. Westerhof Debbie R. van Raaij Marloes van Adrichem Andreas D. Prakasa Jose L. Lozano‐Torres Jaap Bakker Geert Smant Arjen Schots

Transforming growth factor beta (TGF-β) is a signalling molecule that plays a key role in developmental and immunological processes in mammals. Three TGF-β isoforms exist in humans, and each isoform has unique therapeutic potential. Plants offer a platform for the production of recombinant proteins, which is cheap and easy to scale up and has a low risk of contamination with human pathogens. TG...

Journal: :The Journal of biological chemistry 2003
Ying-Zhi Xu Yun Ji Birgit Zipser John Jellies Kristen M Johansen Jorgen Johansen

Tractin is a member of the L1 family of cell adhesion molecules in leech. Immunoblot analysis suggests that Tractin is constitutively cleaved in vivo at a proteolytic site with the sequence RKRRSR. This sequence conforms to the consensus sequence for cleavage by members of the furin family of convertases, and this proteolytic site is shared by a majority of other L1 family members. We provide e...

Journal: :The Biochemical journal 1996
M Santavicca A Noel H Angliker I Stoll J P Segain P Anglard M Chretien N Seidah P Basset

Stromelysin-3 (ST3) is a matrix metalloproteinase (MMP) which has been implicated in cancer progression and in a number of conditions involving tissue remodelling. In contrast to other MMPs which are secreted as zymogens requiring extracellular activation, ST3 is found in the extracellular space as a potentially active mature form, suggesting that the activation of the ST3 proform differs from ...

Journal: :The Journal of pharmacology and experimental therapeutics 2004
Fraser D Russell Philip Kearns Istvan Toth Peter Molenaar

Human urotensin-II (hU-II) is processed from its prohormone (ProhU-II) at putative cleavage sites for furin and serine proteases such as trypsin. Although proteolysis is required for biological activity, the endogenous "urotensin-converting enzyme" (UCE) has not been investigated. The aim of this study was to investigate UCE activity in cultured human cells and in blood, comparing activity with...

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