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. 2020 Dec 11;11:6349. doi: 10.1038/s41467-020-20227-8

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© The Author(s) 2020

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 1 — a CryoEM image of the amyloid fibrils formed by hnRNPA1 LC. Fibrils formed by hnRNPA1 LC purified in four independent experiments provide reproducible images. b CryoEM 3D reconstruction of the hnRNPA1 LC fibril. c CryoEM density map of the hnRNPA1 LC fibril. Fibril parameters including fibril width, half pitch, twist angle, and rise are marked. Protofilaments are colored in magenta and orange individually. The map was prepared by UCSF Chimera v1.13. d Cross-section view of the density map with structure model built upon it. Protofilaments are in different colors.