Preference toward a polylysine enantiomer in inhibiting prions
- Authors
- Jackson, Karen S.; Yeom, Jihyun; Han, Youngmi; Bae, Younsoo; Ryou, Chongsuk
- Issue Date
- Mar-2013
- Publisher
- Springer Verlag
- Keywords
- Polylysine; Enantiomers; Prion; Inhibition; Plasminogen
- Citation
- Amino Acids, v.44, no.3, pp 993 - 1000
- Pages
- 8
- Indexed
- SCI
SCIE
SCOPUS
- Journal Title
- Amino Acids
- Volume
- 44
- Number
- 3
- Start Page
- 993
- End Page
- 1000
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/28822
- DOI
- 10.1007/s00726-012-1430-8
- ISSN
- 0939-4451
1438-2199
- Abstract
- Differential anti-prion activity of polylysine enantiomers was studied. Based on our recent discovery that poly-l-lysine (PLK) is a potent anti-prion agent, we investigated suppression of prions in cultured cells using poly-d-lysine (PDK). The results showed that PDK was more efficacious than PLK to inhibit prions. Protein misfolding cyclic amplification assay demonstrated improved efficacy of PDK in inhibiting plasminogen-mediated prion propagation, corresponding to the enantio-preference of PDK observed in cultured cells. Furthermore, our study demonstrated that polylysines formed a complex with plasminogen. These results propose to hypothesize a plausible mechanism that elicits prion inhibition by polylysine enantiomers.
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