Did the prion protein become vulnerable to misfolding after an evolutionary divide and conquer event? Article

Richmond, K, Masterson, P, Ortiz, JF et al. (2014). Did the prion protein become vulnerable to misfolding after an evolutionary divide and conquer event? . JOURNAL OF BIOMOLECULAR STRUCTURE & DYNAMICS, 32(7), 1074-1084. 10.1080/07391102.2013.809022

cited authors

  • Richmond, K; Masterson, P; Ortiz, JF; Siltberg-Liberles, J

authors

abstract

  • Despite high sequence identity among mammalian prion proteins (PrPs), mammals have varying rates of susceptibility to prion disease resulting in a so-called species barrier. The species barrier follows no clear pattern, with closely related species or similar sequences being no more likely to infect each other, and remains an unresolved enigma. Variation of the conformationally flexible regions may alter the thermodynamics of the conformational change, commonly referred to as the conformational conversion, which occurs in the pathogenic process of the mammalian prion protein. A conformational ensemble scenario is supported by the species barrier in prion disease and evidence that there are strains of pathogenic prion with different conformations within species. To study how conformational flexibility has evolved in the prion protein, an investigation was undertaken on the evolutionary dynamics of structurally disordered regions in the mammalian prion protein, non-mammalian prion protein that is not vulnerable to prion disease, and remote homologs Doppel and Shadoo. Structural disorder prediction analyzed in an evolutionary context revealed that the occurrence of increased or altered conformational flexibility in mammalian PrPs coincides with key events among PrP, Doppel, and Shadoo. Comparatively rapid evolutionary dynamics of conformational flexibility in the prion protein suggest that the species barrier is not a static phenomenon. A small number of amino acid substitutions can repopulate the conformational ensemble and have a disproportionately large effect on pathogenesis. © 2013 © 2013 Taylor & Francis.

publication date

  • July 3, 2014

published in

Digital Object Identifier (DOI)

start page

  • 1074

end page

  • 1084

volume

  • 32

issue

  • 7