%0 Journal Article
%T Substantially improved pharmacokinetics of recombinant human butyrylcholinesterase by fusion to human serum albumin
%A Yue-Jin Huang
%A Paul M Lundy
%A Anthoula Lazaris
%A Yue Huang
%A Hernan Baldassarre
%A Bin Wang
%A Carl Turcotte
%A M¨¦lanie C£¿t¨¦
%A Annie Bellemare
%A Annie S Bilodeau
%A Sandra Brouillard
%A Madjid Touati
%A Peter Herskovits
%A Isabelle B¨¦gin
%A Nathalie Neveu
%A Eric Brochu
%A Janice Pierson
%A Duncan K Hockley
%A Douglas M Cerasoli
%A David E Lenz
%A Harvey Wilgus
%A Costas N Karatzas
%A Solomon Langermann
%J BMC Biotechnology
%D 2008
%I BioMed Central
%R 10.1186/1472-6750-8-50
%X Secretion level of the fusion protein produced in vitro in BHK cells was ~30 mg/liter. Transgenic mice and goats generated with the fusion constructs expressed in their milk a bioactive protein at concentrations of 0.04¨C1.1 g/liter. BChE activity gel staining and a size exclusion chromatography (SEC)-HPLC revealed that the fusion protein consisted of predominant dimers and some monomers. The protein was confirmed to have expected molecular mass of ~150 kDa by Western blot. The purified fusion protein produced in vitro was injected intravenously into juvenile pigs for pharmacokinetic study. Analysis of a series of blood samples using the Ellman assay revealed a substantial enhancement of the plasma half-life of the fusion protein (~32 h) when compared with a transgenically produced huBChE preparation containing >70% tetramer (~3 h). In vitro nerve agent binding and inhibition experiments indicated that the fusion protein in the milk of transgenic mice had similar inhibition characteristics compared to human plasma BChE against the nerve agents tested.Both the pharmacokinetic study and the in vitro nerve agent binding and inhibition assay suggested that a fusion protein retaining both properties of huBChE and hSA is produced in vitro and in vivo. The production of the fusion protein in the milk of transgenic goats provided further evidence that sufficient quantities of BChE/hSA can be produced to serve as a cost-effective and reliable source of BChE for prophylaxis and post-exposure treatment.Poisoning with organophosphorus (OP) compounds is a severe problem facing military personnel who may encounter lethal doses of these compounds in chemical warfare situations. Further, OP and other anticholinesterase agents are extensively used as pesticides and pose a substantial occupational and environmental risk. Human serum butyrylcholinesterase (huBChE, EC 3.1.1.8) is a globular, tetrameric molecule with a molecular mass of ~340 kDa [1]. Administration of exogenous huBChE ha
%U http://www.biomedcentral.com/1472-6750/8/50