| Title |
Artificial strain of human prions created in vitro / |
| Authors |
Kim, Chae ; Xiao, Xiangzhu ; Chen, Shugui ; Haldiman, Tracy ; Smirnovas, Vytautas ; Kofskey, Diane ; Warren, Miriam ; Surewicz, Krystyna ; Maurer, Nicholas R ; Kong, Qingzhong ; Surewicz, Witold ; Safar, Jiri G |
| DOI |
10.1038/s41467-018-04584-z |
| Full Text |
|
| Is Part of |
Nature communications.. London : Nature Publishing Group. 2018, vol. 9, art. no. 2166, p. [1-11].. eISSN 2041-1723 |
| Keywords [eng] |
Creutzfeldt-Jakob-disease ; bovine spongiform encephalopathy ; protein amyloid fibrils ; chronic wasting disease ; transgenic mice ; hydrogen/deuterium exchange ; distinct structures ; Alzheimers-disease ; cofactor molecules ; infectious prions |
| Abstract [eng] |
The molecular mechanism that determines under physiological conditions transmissibility of the most common human prion disease, sporadic Creutzfeldt-Jakob disease (sCJD) is unknown. We report the synthesis of new human prion from the recombinant human prion protein expressed in bacteria in reaction seeded with sCJD MM1 prions and cofactor, ganglioside GM1. These synthetic human prions were infectious to transgenic mice expressing non-glycosylated human prion protein, causing neurologic dysfunction after 459 and 224 days in the first and second passage, respectively. The neuropathology, replication potency, and biophysical profiling suggest that a novel, particularly neurotoxic human prion strain was created. Distinct biological and structural characteristics of our synthetic human prions suggest that subtle changes in the structural organization of critical domains, some linked to posttranslational modifications of the pathogenic prion protein (PrPSc), play a crucial role as a determinant of human prion infectivity, host range, and targetting of specific brain structures in mice models. |
| Published |
London : Nature Publishing Group |
| Type |
Journal article |
| Language |
English |
| Publication date |
2018 |
