Molecular mechanism of enantioselective proton transfer to carbon in catalytic antibody 14D9
AUTOR(ES)
Zheng, Lei
FONTE
National Academy of Sciences
RESUMO
Catalytic antibody 14D9 catalyzes the enantioselective protonation of prochiral enol ethers with high enantioselectivity (>99% ee) and a practical turnover (kcat = 0.4 s-1), allowing for preparative scale applications. This antibody represents one of the rare examples of catalytic antibodies promoting acid-catalyzed processes. Antibody 14D9 was cloned and expressed as a chimeric Fab fragment in Escherichia coli. Crystal structures of Fab 14D9 as apo form and of its close analog 19C9 in complex with the transition state analog were determined at 2.8-Å resolution. A series of site-directed mutagenesis experiments was carried out to probe the role of individual active-site amino acids. Proton transfer to carbon is catalyzed by a hydrogen bond network formed by the side chains of AspH101 and TyrL36 with a water molecule serving as a relay. The intermediate oxocarbonium ion formed during the protonation step is trapped by the same water molecule, resulting in an overall syn-addition of water to the enol ether's double bond. The enantioselectivity is caused by steric crowding at the active site, mainly because of the side chain of PheH84. The 20-fold lower activity of 19C9 compared with 14D9 was traced down to residue ThrL46, which forms a nonproductive hydrogen bond with the catalytic residue AspH101, which competes with the critical AspH101—TyrL36 hydrogen bond and therefore reduces catalytic efficiency. The catalytic activity of 19C9 was restored to that of 14D9 by using either site-directed mutagenesis (ThrL46Ala) or chain shuffling.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=376184Documentos Relacionados
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