Learning to automate cryo-electron microscopy data collection with
Ptolemy
- URL: http://arxiv.org/abs/2112.01534v1
- Date: Wed, 1 Dec 2021 22:39:28 GMT
- Title: Learning to automate cryo-electron microscopy data collection with
Ptolemy
- Authors: Paul T. Kim, Alex J. Noble, Anchi Cheng, Tristan Bepler
- Abstract summary: cryogenic electron microscopy (cryo-EM) has emerged as a primary method for determining near-native, near-atomic resolution 3D structures of biological macromolecules.
Currently, the process of collecting high-magnification cryo-EM micrographs requires human input and manual tuning of parameters.
Here, we develop the first pipeline to automate low- and medium-magnification targeting with purpose-built algorithms.
- Score: 4.6453787256723365
- License: http://creativecommons.org/licenses/by/4.0/
- Abstract: Over the past decade, cryogenic electron microscopy (cryo-EM) has emerged as
a primary method for determining near-native, near-atomic resolution 3D
structures of biological macromolecules. In order to meet increasing demand for
cryo-EM, automated methods to improve throughput and efficiency while lowering
costs are needed. Currently, the process of collecting high-magnification
cryo-EM micrographs, data collection, requires human input and manual tuning of
parameters, as expert operators must navigate low- and medium-magnification
images to find good high-magnification collection locations. Automating this is
non-trivial: the images suffer from low signal-to-noise ratio and are affected
by a range of experimental parameters that can differ for each collection
session. Here, we use various computer vision algorithms, including mixture
models, convolutional neural networks (CNNs), and U-Nets to develop the first
pipeline to automate low- and medium-magnification targeting with purpose-built
algorithms. Learned models in this pipeline are trained on a large internal
dataset of images from real world cryo-EM data collection sessions, labeled
with locations that were selected by operators. Using these models, we show
that we can effectively detect and classify regions of interest (ROIs) in low-
and medium-magnification images, and can generalize to unseen sessions, as well
as to images captured using different microscopes from external facilities. We
expect our pipeline, Ptolemy, will be both immediately useful as a tool for
automation of cryo-EM data collection, and serve as a foundation for future
advanced methods for efficient and automated cryo-EM microscopy.
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