Abstract
In prion inheritance and transmission, strains are phenotypic variants encoded by protein 'conformations'. However, it is unclear how a protein conformation can be stable enough to endure transmission between cells or organisms. Here we describe new polymorphic crystal structures of segments of prion and other amyloid proteins, which offer two structural mechanisms for the encoding of prion strains. In packing polymorphism, prion strains are encoded by alternative packing arrangements (polymorphs) of β-sheets formed by the same segment of a protein; in segmental polymorphism, prion strains are encoded by distinct β-sheets built from different segments of a protein. Both forms of polymorphism can produce enduring conformations capable of encoding strains. These molecular mechanisms for transfer of protein-encoded information into prion strains share features with the familiar mechanism for transfer of nucleic acidâencoded information into microbial strains, including sequence specificity and recognition by noncovalent bonds.
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Acknowledgements
We thank the NE-CAT beamline at the Advanced Photon Source and ID-13 beamline at the European Synchrotron Radiation Facility for beam time and collection assistance, and the National Science Foundation, National Institutes of Health and Howard Hughes Medical Institute for financial support, and P. Chien for discussion.
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J.J.W.W., M.L., R.N., M.I.A. and M.R.S. planned, executed and analyzed the research and coauthored the paper; L.G. planned and analyzed the research; A.B.S. executed and analyzed the research; D.C. and K.R. collected the X-ray diffraction data; and D.E. supervised the research and coauthored the paper.
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Wiltzius, J., Landau, M., Nelson, R. et al. Molecular mechanisms for protein-encoded inheritance. Nat Struct Mol Biol 16, 973â978 (2009). https://doi.org/10.1038/nsmb.1643
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DOI: https://doi.org/10.1038/nsmb.1643
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