Journal article

Star Polymers Reduce Islet Amyloid Polypeptide Toxicity via Accelerated Amyloid Aggregation

EH Pilkington, M Lai, X Ge, WJ Stanley, B Wang, M Wang, A Kakinen, MA Sani, MR Whittaker, EN Gurzov, F Ding, JF Quinn, TP Davis, PC Ke

Biomacromolecules | AMER CHEMICAL SOC | Published : 2017

Abstract

Protein aggregation into amyloid fibrils is a ubiquitous phenomenon across the spectrum of neurodegenerative disorders and type 2 diabetes. A common strategy against amyloidogenesis is to minimize the populations of toxic oligomers and protofibrils by inhibiting protein aggregation with small molecules or nanoparticles. However, melanin synthesis in nature is realized by accelerated protein fibrillation to circumvent accumulation of toxic intermediates. Accordingly, we designed and demonstrated the use of star-shaped poly(2-hydroxyethyl acrylate) (PHEA) nanostructures for promoting aggregation while ameliorating the toxicity of human islet amyloid polypeptide (IAPP), the peptide involved in ..

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University of Melbourne Researchers

Grants

Awarded by Juvenile Diabetes Research Foundation International


Funding Acknowledgements

This work was supported by ARC Project CE140100036 (T.P.D.), NSF CAREER CBET-1553945 (F.D.), NIH MIRA R35GM119691 (F.D.), NHMRC project grant APP1071350 (E.N.G.), and the Monash Institute of Pharmaceutical Sciences (P.C.K.). T.P.D. is thankful for the award of an Australian Laureate Fellowship from the ARC. J.F.Q, acknowledges receipt of a Future Fellowship from the ARC. E.H.P. acknowledges the support of an Australian Government Research Training Program scholarship. E.N.G. is supported by Juvenile Diabetes Research Foundation (JDRF) fellowship.