Unraveling infectious structures, strain variants and species barriers for the yeast prion [PSI+]

被引:61
|
作者
Tessier, Peter M. [1 ]
Lindquist, Susan [2 ]
机构
[1] Rensselaer Polytech Inst, Ctr Biotechnol & Interdisciplinary Studies, Dept Chem & Biol Engn, Troy, NY 12180 USA
[2] MIT, Whitehead Inst Biomed Res, Cambridge Ctr 9, Dept Biol,Howard Hughes Med Inst, Cambridge, MA USA
基金
美国国家卫生研究院;
关键词
AMYLOID FIBRIL STRUCTURE; SACCHAROMYCES-CEREVISIAE; IN-VITRO; SUP35; PROTEIN; TRANSGENIC MICE; MOLECULAR-BASIS; EPIGENETIC REGULATION; ENVIRONMENTAL-STRESS; PODOSPORA-ANSERINA; GENETIC-VARIATION;
D O I
10.1038/nsmb.1617
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Prions are proteins that can access multiple conformations, at least one of which is beta-sheet rich, infectious and self-perpetuating in nature. These infectious proteins show several remarkable biological activities, including the ability to form multiple infectious prion conformations, also known as strains or variants, encoding unique biological phenotypes, and to establish and overcome prion species (transmission) barriers. In this Perspective, we highlight recent studies of the yeast prion [PSI+], using various biochemical and structural methods, that have begun to illuminate the molecular mechanisms by which self-perpetuating prions encipher such biological activities. We also discuss several aspects of prion conformational change and structure that remain either unknown or controversial, and we propose approaches to accelerate the understanding of these enigmatic, infectious conformers.
引用
收藏
页码:598 / 605
页数:8
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