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Total synthesis of biotinylated N domain of human hepatocyte growth factor
Authors:Laurent Raibaut  Jérome Vicogne  Bérénice Leclercq  Hervé Drobecq  Rémi Desmet  Oleg Melnyk
Institution:1. Max Planck Institut (MPI) für Molekulare Physiologie, Dept. of Chemical Biology, Otto-Hahn-Strasse 11, Dortmund, 44026, Germany
Abstract:Hepatocyte growth factor/scatter factor (HGF/SF) is the high affinity ligand of MET tyrosine kinase receptor. We report here the total synthesis of a biotinylated analogue of human HGF/SF N domain. Functionally, N domain is part of the HGF/SF high affinity binding site for MET and also the main HGF/SF binding site for heparin. The 97 Aa linear chain featuring a C-terminal biotin group was assembled in high yield using an N-to-C one-pot three segments assembly strategy relying on a sequential Native Chemical Ligation (NCL)/bis(2-sulfanylethyl)amido (SEA) native peptide ligation process. The folded protein displayed the native disulfide bond pattern and showed the ability to bind heparin.
Keywords:Protein total synthesis  Bis(2-sulfanylethyl)amido (SEA)  One-pot assembly  Native chemical ligation (NCL)  Hepatocyte growth factor/scatter factor (HGF/SF)
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