Papers

International journal
Dec, 2017

Flow-aligned, single-shot fiber diffraction using a femtosecond X-ray free-electron laser.

Cytoskeleton (Hoboken, N.J.)
  • David Popp
  • N Duane Loh
  • Habiba Zorgati
  • Umesh Ghoshdastider
  • Lu Ting Liow
  • Magdalena I Ivanova
  • Mårten Larsson
  • Daniel P DePonte
  • Richard Bean
  • Kenneth R Beyerlein
  • Cornelius Gati
  • Dominik Oberthuer
  • David Arnlund
  • Gisela Brändén
  • Peter Berntsen
  • Duilio Cascio
  • Leonard M G Chavas
  • Joe P J Chen
  • Ke Ding
  • Holger Fleckenstein
  • Lars Gumprecht
  • Rajiv Harimoorthy
  • Estelle Mossou
  • Michael R Sawaya
  • Aaron S Brewster
  • Johan Hattne
  • Nicholas K Sauter
  • Marvin Seibert
  • Carolin Seuring
  • Francesco Stellato
  • Thomas Tilp
  • David S Eisenberg
  • Marc Messerschmidt
  • Garth J Williams
  • Jason E Koglin
  • Lee Makowski
  • Rick P Millane
  • Trevor Forsyth
  • Sébastien Boutet
  • Thomas A White
  • Anton Barty
  • Henry Chapman
  • Swaine L Chen
  • Mengning Liang
  • Richard Neutze
  • Robert C Robinson
  • Display all

Volume
74
Number
12
First page
472
Last page
481
Language
English
Publishing type
Research paper (scientific journal)
DOI
10.1002/cm.21378
Publisher
WILEY

A major goal for X-ray free-electron laser (XFEL) based science is to elucidate structures of biological molecules without the need for crystals. Filament systems may provide some of the first single macromolecular structures elucidated by XFEL radiation, since they contain one-dimensional translational symmetry and thereby occupy the diffraction intensity region between the extremes of crystals and single molecules. Here, we demonstrate flow alignment of as few as 100 filaments (Escherichia coli pili, F-actin, and amyloid fibrils), which when intersected by femtosecond X-ray pulses result in diffraction patterns similar to those obtained from classical fiber diffraction studies. We also determine that F-actin can be flow-aligned to a disorientation of approximately 5 degrees. Using this XFEL-based technique, we determine that gelsolin amyloids are comprised of stacked β-strands running perpendicular to the filament axis, and that a range of order from fibrillar to crystalline is discernable for individual α-synuclein amyloids.

Link information
DOI
https://doi.org/10.1002/cm.21378
PubMed
https://www.ncbi.nlm.nih.gov/pubmed/28574190
Web of Science
https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=JSTA_CEL&SrcApp=J_Gate_JST&DestLinkType=FullRecord&KeyUT=WOS:000417746200005&DestApp=WOS_CPL
ID information
  • DOI : 10.1002/cm.21378
  • ISSN : 1949-3584
  • eISSN : 1949-3592
  • Pubmed ID : 28574190
  • Web of Science ID : WOS:000417746200005

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