Abstract
An improved analysis for single-particle imaging (SPI) experiments, using the limited data, is presented here. Results are based on a study of bacteriophage PR772 performed at the Atomic, Molecular and Optical Science instrument at the Linac Coherent Light Source as part of the SPI initiative. Existing methods were modified to cope with the shortcomings of the experimental data: inaccessibility of information from half of the detector and a small fraction of single hits. The general SPI analysis workflow was upgraded with the expectation-maximization based classification of diffraction patterns and mode decomposition on the final virus-structure determination step. The presented processing pipeline allowed us to determine the 3D structure of bacteriophage PR772 without symmetry constraints with a spatial resolution of 6.9 nm. The obtained resolution was limited by the scattering intensity during the experiment and the relatively small number of single hits.
Funder
Helmholtz Association
Russian Science Foundation
BioXFEL Science and Technology Center
European Regional Development Fund
Ministerstvo Školství, Mládeže a Tělovýchovy
European Research Council
Human Frontier Science Program
Joachim Herz Stiftung
Vetenskapsrådet
Knut och Alice Wallenbergs Stiftelse
Röntgen-Ångström Cluster
Türkiye Bilimsel ve Teknolojik Araştirma Kurumu
Publisher
International Union of Crystallography (IUCr)
Subject
Condensed Matter Physics,General Materials Science,Biochemistry,General Chemistry
Cited by
17 articles.
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