» Articles » PMID: 27845625

Accelerated Cryo-EM Structure Determination with Parallelisation Using GPUs in RELION-2

Overview
Journal Elife
Specialty Biology
Date 2016 Nov 16
PMID 27845625
Citations 549
Authors
Affiliations
Soon will be listed here.
Abstract

By reaching near-atomic resolution for a wide range of specimens, single-particle cryo-EM structure determination is transforming structural biology. However, the necessary calculations come at large computational costs, which has introduced a bottleneck that is currently limiting throughput and the development of new methods. Here, we present an implementation of the RELION image processing software that uses graphics processors (GPUs) to address the most computationally intensive steps of its cryo-EM structure determination workflow. Both image classification and high-resolution refinement have been accelerated more than an order-of-magnitude, and template-based particle selection has been accelerated well over two orders-of-magnitude on desktop hardware. Memory requirements on GPUs have been reduced to fit widely available hardware, and we show that the use of single precision arithmetic does not adversely affect results. This enables high-resolution cryo-EM structure determination in a matter of days on a single workstation.

Citing Articles

MERS-CoV spike vaccine-induced N-terminal domain-specific antibodies are more protective than receptor binding domain-specific antibodies.

Abiona O, Wang N, Leist S, Schafer A, Cockrell A, Wang L iScience. 2025; 28(2):111632.

PMID: 39898019 PMC: 11783452. DOI: 10.1016/j.isci.2024.111632.


Scaffold-enabled high-resolution cryo-EM structure determination of RNA.

Haack D, Rudolfs B, Jin S, Khitun A, Weeks K, Toor N Nat Commun. 2025; 16(1):880.

PMID: 39837824 PMC: 11751092. DOI: 10.1038/s41467-024-55699-5.


The nucleocapsid architecture and structural atlas of the prototype baculovirus define the hallmarks of a new viral realm.

Johnstone B, Hardy J, Ha J, Butkovic A, Koszalka P, Accurso C Sci Adv. 2024; 10(51):eado2631.

PMID: 39693434 PMC: 11654684. DOI: 10.1126/sciadv.ado2631.


Structural basis of respiratory complex adaptation to cold temperatures.

Shin Y, Latorre-Muro P, Djurabekova A, Zdorevskyi O, Bennett C, Burger N Cell. 2024; 187(23):6584-6598.e17.

PMID: 39395414 PMC: 11601890. DOI: 10.1016/j.cell.2024.09.029.


A potent pan-sarbecovirus neutralizing antibody resilient to epitope diversification.

Rosen L, Tortorici M, De Marco A, Pinto D, Foreman W, Taylor A Cell. 2024; 187(25):7196-7213.e26.

PMID: 39383863 PMC: 11645210. DOI: 10.1016/j.cell.2024.09.026.


References
1.
Roseman A . Particle finding in electron micrographs using a fast local correlation algorithm. Ultramicroscopy. 2003; 94(3-4):225-36. DOI: 10.1016/s0304-3991(02)00333-9. View

2.
Grigorieff N . FREALIGN: high-resolution refinement of single particle structures. J Struct Biol. 2006; 157(1):117-25. DOI: 10.1016/j.jsb.2006.05.004. View

3.
Tang G, Peng L, Baldwin P, Mann D, Jiang W, Rees I . EMAN2: an extensible image processing suite for electron microscopy. J Struct Biol. 2006; 157(1):38-46. DOI: 10.1016/j.jsb.2006.05.009. View

4.
Hohn M, Tang G, Goodyear G, Baldwin P, Huang Z, Penczek P . SPARX, a new environment for Cryo-EM image processing. J Struct Biol. 2006; 157(1):47-55. DOI: 10.1016/j.jsb.2006.07.003. View

5.
Heymann J, Belnap D . Bsoft: image processing and molecular modeling for electron microscopy. J Struct Biol. 2006; 157(1):3-18. DOI: 10.1016/j.jsb.2006.06.006. View