Pregled bibliografske jedinice broj: 648465
NMR Structural Studies of Human Cellular Prion Proteins
NMR Structural Studies of Human Cellular Prion Proteins // Current topics in medicinal chemistry, 13 (2013), 19; 2407-2418 doi:10.2174/15680266113136660169 (međunarodna recenzija, pregledni rad, znanstveni)
CROSBI ID: 648465 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
NMR Structural Studies of Human Cellular Prion
Proteins
Autori
Biljan, Ivana ; Ilc, Gregor ; Giachin, Gabriele ; Legname, Giuseppe ; Plavec, Janez
Izvornik
Current topics in medicinal chemistry (1568-0266) 13
(2013), 19;
2407-2418
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, pregledni rad, znanstveni
Ključne riječi
Mutant ; NMR structure ; pH ; prion protein ; protective polymorphism ; transmissible spongiform encephalopathy
Sažetak
Prion diseases or transmissible spongiform encephalopathies (TSEs) are fatal neurodegenerative disorders associated with the conformational conversion of the cellular prion protein, PrPC, into a pathological form known as prion or PrPSc. They can be classified into sporadic, inherited and infectious forms. Spontaneous generation of PrPSc in inherited forms of prion diseases is caused by mutations in the human prion protein gene (PRNP). A major goal in prion biology is unraveling the molecular mechanism by which PrPC misfolds and leads to development of diseases. Structural characterization of various human PrP (HuPrP) variants may be helpful for better understanding of the earliest stages of the conformational changes leading to spontaneous generation of prions. Here, we review the results of the recent high-resolution nuclear magnetic resonance (NMR) structural studies on HuPrPs with pathological Q212P and V210I mutations linked with Gerstmann-Sträussler- Scheinker (GSS) syndrome and familial Creutzfeldt-Jakob disease (fCJD), respectively, and HuPrP carrying naturally occurring E219K polymorphism considered to protect against sporadic CJD (sCJD). We describe subtle local differences between the three-dimensional (3D) structures of HuPrP mutants and the wild-type (WT) protein, providing new insights into the possible key structural determinants underlying conversion of PrPC into PrPSc. Also highlighted are the most recent findings from NMR studies about the effect of pH on the structural features of HuPrP with V210I mutation.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
Citiraj ovu publikaciju:
Časopis indeksira:
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE