Literature DB >> 32233514

Live Analysis and Reconstruction of Single-Particle Cryo-Electron Microscopy Data with CryoFLARE.

Andreas D Schenk1, Simone Cavadini1, Nicolas H Thomä1, Christel Genoud1.   

Abstract

Efficient, reproducible and accountable single-particle cryo-electron microscopy structure determination is tedious and often impeded by the lack of a standardized procedure for data analysis and processing. To address this issue, we have developed the FMI Live Analysis and Reconstruction Engine (CryoFLARE). CryoFLARE is a modular open-source platform offering easy integration of new processing algorithms developed by the cryo-EM community. It provides a user-friendly interface that allows fast setup of standardized workflows, serving the need of pharmaceutical industry and academia alike who need to optimize throughput of their microscope. To consistently document how data is processed, CryoFLARE contains an integrated reporting facility to create reports. Live analysis and processing parallel to data acquisition are used to monitor and optimize data quality. Problems at the level of the sample preparation (heterogeneity, ice thickness, sparse particles, areas selected for acquisition, etc.) or misalignments of the microscope optics can quickly be detected and rectified before data collection is continued. Interfacing with automated data collection software for retrieval of acquisition metadata reduces user input needed for analysis, and with it minimizes potential sources of errors and workflow inconsistencies. Local and remote export support in Relion-compatible job and data format allows seamless integration into the refinement process. The support for nonlinear workflows and fine-grained scheduling for mixed workflows with separate CPU and GPU based calculation steps ensures optimal use of processing hardware. CryoFLARE's flexibility allows it to be used for all types of image acquisitions, ranging from sample screening to high-resolution data collection, and it offers a new alternative for setting up image processing workflows. It can be used without modifications of the hardware/software delivered by the microscope supplier. As it runs on a server in parallel to the hardware used for acquisition, it can easily be set up for remote display connections and fast control of the acquisition status.

Mesh:

Year:  2020        PMID: 32233514     DOI: 10.1021/acs.jcim.9b01102

Source DB:  PubMed          Journal:  J Chem Inf Model        ISSN: 1549-9596            Impact factor:   4.956


  7 in total

1.  Structural insights into Fe-S protein biogenesis by the CIA targeting complex.

Authors:  Susanne A Kassube; Nicolas H Thomä
Journal:  Nat Struct Mol Biol       Date:  2020-07-06       Impact factor: 15.369

2.  Faces of Contemporary CryoEM Information and Modeling.

Authors:  Giulia Palermo; Yuji Sugita; Willy Wriggers; Rommie E Amaro
Journal:  J Chem Inf Model       Date:  2020-05-26       Impact factor: 4.956

3.  Structural mechanism of cGAS inhibition by the nucleosome.

Authors:  Ganesh R Pathare; Alexiane Decout; Selene Glück; Simone Cavadini; Kristina Makasheva; Ruud Hovius; Georg Kempf; Joscha Weiss; Zuzanna Kozicka; Baptiste Guey; Pauline Melenec; Beat Fierz; Nicolas H Thomä; Andrea Ablasser
Journal:  Nature       Date:  2020-09-10       Impact factor: 49.962

4.  New tools for automated cryo-EM single-particle analysis in RELION-4.0.

Authors:  Dari Kimanius; Liyi Dong; Grigory Sharov; Takanori Nakane; Sjors H W Scheres
Journal:  Biochem J       Date:  2021-12-22       Impact factor: 3.857

5.  Structure of the ciliogenesis-associated CPLANE complex.

Authors:  Gerasimos Langousis; Simone Cavadini; Niels Boegholm; Esben Lorentzen; Georg Kempf; Patrick Matthias
Journal:  Sci Adv       Date:  2022-04-15       Impact factor: 14.957

6.  TranSPHIRE: automated and feedback-optimized on-the-fly processing for cryo-EM.

Authors:  Markus Stabrin; Fabian Schoenfeld; Thorsten Wagner; Sabrina Pospich; Christos Gatsogiannis; Stefan Raunser
Journal:  Nat Commun       Date:  2020-11-11       Impact factor: 14.919

7.  Structure of the human C9orf72-SMCR8 complex reveals a multivalent protein interaction architecture.

Authors:  Julia Nörpel; Simone Cavadini; Andreas D Schenk; Alexandra Graff-Meyer; Daniel Hess; Jan Seebacher; Jeffrey A Chao; Varun Bhaskar
Journal:  PLoS Biol       Date:  2021-07-23       Impact factor: 8.029

  7 in total

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