Sub-pixel electron detection using a convolutional neural network.

Cryo-EM Detectors Neural network Structural biology

Journal

Ultramicroscopy
ISSN: 1879-2723
Titre abrégé: Ultramicroscopy
Pays: Netherlands
ID NLM: 7513702

Informations de publication

Date de publication:
11 2020
Historique:
received: 05 02 2020
revised: 28 07 2020
accepted: 02 08 2020
pubmed: 25 8 2020
medline: 25 8 2020
entrez: 25 8 2020
Statut: ppublish

Résumé

Modern direct electron detectors (DEDs) provided a giant leap in the use of cryogenic electron microscopy (cryo-EM) to study the structures of macromolecules and complexes thereof. However, the currently available commercial DEDs, all based on the monolithic active pixel sensor, still require relative long exposure times and their best results have only been obtained at 300 keV. There is a need for pixelated electron counting detectors that can be operated at a broader range of energies, at higher throughput and higher dynamic range. Hybrid Pixel Detectors (HPDs) of the Medipix family were reported to be unsuitable for cryo-EM at energies above 80 keV as those electrons would affect too many pixels. Here we show that the Timepix3, part of the Medipix family, can be used for cryo-EM applications at higher energies. We tested Timepix3 detectors on a 200 keV FEI Tecnai Arctica microscope and a 300 keV FEI Tecnai G2 Polara microscope. A correction method was developed to correct for per-pixel differences in output. Timepix3 data were simulated for individual electron events using the package Geant4Medipix. Global statistical characteristics of the simulated detector response were in good agreement with experimental results. A convolutional neural network (CNN) was trained using the simulated data to predict the incident position of the electron within a pixel cluster. After training, the CNN predicted, on average, 0.50 pixel and 0.68 pixel from the incident electron position for 200 keV and 300 keV electrons respectively. The CNN improved the MTF of experimental data at half Nyquist from 0.39 to 0.70 at 200 keV, and from 0.06 to 0.65 at 300 keV respectively. We illustrate that the useful dose-lifetime of a protein can be measured within a 1 second exposure using Timepix3.

Identifiants

pubmed: 32835904
pii: S0304-3991(20)30242-4
doi: 10.1016/j.ultramic.2020.113091
pii:
doi:

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

113091

Informations de copyright

Copyright © 2020 The Authors. Published by Elsevier B.V. All rights reserved.

Auteurs

J Paul van Schayck (JP)

Maastricht MultiModal Molecular Imaging Institute (M4I), FHML, Maastricht University, Maastricht, The Netherlands.

Eric van Genderen (E)

BIO, Laboratory for Nanoscale Biology. Paul Scherrer Institut, Villigen CH-5232, Switzerland.

Erik Maddox (E)

Leiden University, Leiden, The Netherlands; Amsterdam Scientific Instruments (ASI), Amsterdam, The Netherlands.

Lucas Roussel (L)

Maastricht MultiModal Molecular Imaging Institute (M4I), FHML, Maastricht University, Maastricht, The Netherlands.

Hugo Boulanger (H)

Maastricht MultiModal Molecular Imaging Institute (M4I), FHML, Maastricht University, Maastricht, The Netherlands.

Erik Fröjdh (E)

PSD Detector Group, Paul Scherrer Institute, Villigen CH-5232, Switzerland.

Jan-Pieter Abrahams (JP)

Leiden University, Leiden, The Netherlands; BIO, Laboratory for Nanoscale Biology. Paul Scherrer Institut, Villigen CH-5232, Switzerland; Center for Cellular Imaging and NanoAnalytics, Biozentrum, University of Basel, Basel CH-4058, Switzerland.

Peter J Peters (PJ)

Maastricht MultiModal Molecular Imaging Institute (M4I), FHML, Maastricht University, Maastricht, The Netherlands.

Raimond B G Ravelli (RBG)

Maastricht MultiModal Molecular Imaging Institute (M4I), FHML, Maastricht University, Maastricht, The Netherlands. Electronic address: rbg.ravelli@maastrichtuniversity.nl.

Classifications MeSH