Cryo-EM of full-length α-synuclein reveals fibril polymorphs with a common structural kernel

Binsen Li(University of California, Los Angeles), P. Ge(California NanoSystems Institute), Kevin A. Murray(Howard Hughes Medical Institute), Phorum Sheth(University of California, Los Angeles), Meng Zhang(Howard Hughes Medical Institute), Gayatri Nair(University of California, Los Angeles), M.R. Sawaya(Howard Hughes Medical Institute), Woo Shik Shin(University of California, Los Angeles), David R. Boyer(Howard Hughes Medical Institute), Shulin Ye(California NanoSystems Institute), David Eisenberg(Howard Hughes Medical Institute), Z. Hong Zhou(California NanoSystems Institute), Lin Jiang(University of California, Los Angeles)
Nature Communications
August 31, 2018
Cited by 645Open Access
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Abstract

α-Synuclein (aSyn) fibrillar polymorphs have distinct in vitro and in vivo seeding activities, contributing differently to synucleinopathies. Despite numerous prior attempts, how polymorphic aSyn fibrils differ in atomic structure remains elusive. Here, we present fibril polymorphs from the full-length recombinant human aSyn and their seeding capacity and cytotoxicity in vitro. By cryo-electron microscopy helical reconstruction, we determine the structures of the two predominant species, a rod and a twister, both at 3.7 Å resolution. Our atomic models reveal that both polymorphs share a kernel structure of a bent β-arch, but differ in their inter-protofilament interfaces. Thus, different packing of the same kernel structure gives rise to distinct fibril polymorphs. Analyses of disease-related familial mutations suggest their potential contribution to the pathogenesis of synucleinopathies by altering population distribution of the fibril polymorphs. Drug design targeting amyloid fibrils in neurodegenerative diseases should consider the formation and distribution of concurrent fibril polymorphs.


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