Protein Modification with Amphiphilic Block Copoly(2-oxazoline)s as a New Platform for Enhanced Cellular Delivery
KAUST Grant NumberKUK-F1-029-32
Online Publication Date2010-06-15
Print Publication Date2010-08-02
Permanent link to this recordhttp://hdl.handle.net/10754/599410
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AbstractSeveral homopolymers, random copolymers and block copolymers based on poly(2-oxazoline)s (POx) were synthesized and conjugated to horseradish peroxidase (HRP) using biodegradable and nonbiodegradable linkers. These conjugates were characterized by amino group titration, polyacrylamide gel electrophoresis (PAGE), isoelectric focusing, enzymatic activity assay and conformation analysis. The conjugates contained on average from about one to two polymer chains per enzyme. From 70% to 90% of enzymatic activity was retained in most cases. Circular dichroism (CD) analysis revealed that HRP modification affected the secondary structure of the apoprotein but did not affect the tertiary structure and heme environment. Enhanced cellular uptake was found in the conjugates of two block copolymers using both MDCK cells and Caco-2 cells, but not in the conjugates of random copolymer and homopolymer. Conjugation with a block copolymer of 2-methyl-2-oxazoline and 2-butyl-2-oxazoline led to the highest cellular uptake as compared to other conjugates. Our data indicates that modification with amphiphilic POx has the potential to modulate and enhance cellular delivery of proteins.
CitationTong J, Luxenhofer R, Yi X, Jordan R, Kabanov AV (2010) Protein Modification with Amphiphilic Block Copoly(2-oxazoline)s as a New Platform for Enhanced Cellular Delivery. Molecular Pharmaceutics 7: 984–992. Available: http://dx.doi.org/10.1021/mp100102p.
SponsorsThis study was supported by the United States National Institutes of Health (NIH) RO1 Grant NS051334, the United States Department of Defense (DoD) USAMRMC 06108004 and the Nanomaterials Core Facility of the Nebraska Center of Nanomedicine supported by NIH COBRE Grant RR021937 (all awarded to A.V.K.). R.L. is also thankful to the Deutsche Akademischen Austauschdienst (DAAD) for a postdoctoral fellowship and to the King Abdullah University of Science and Technology (KAUST) Award No. KUK-F1-029-32 for partial salary support. Likewise X.Y. has been in part supported by the American Heart Association (AHA) Midwest Predoctoral Fellowship 0910040G. We also gratefully acknowledge Professor Luis Marky (College of Pharmacy, UNMC) for kind assistance in CD experiments.
PublisherAmerican Chemical Society (ACS)
PubMed Central IDPMC3070747
CollectionsPublications Acknowledging KAUST Support
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