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An Algorithm for Enhancing the Image Contrast of Electron Tomography

Three-dimensional (3D) reconstruction of a single protein molecule is essential for understanding the relationship between the structural dynamics and functions of the protein. Electron tomography (ET) provides a tool for imaging an individual particle of protein from a series of tilted angles. Indi...

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Detalles Bibliográficos
Autores principales: Wu, Hao, Zhai, Xiaobo, Lei, Dongsheng, Liu, Jianfang, Yu, Yadong, Bie, Rongfang, Ren, Gang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232092/
https://www.ncbi.nlm.nih.gov/pubmed/30420636
http://dx.doi.org/10.1038/s41598-018-34652-9
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author Wu, Hao
Zhai, Xiaobo
Lei, Dongsheng
Liu, Jianfang
Yu, Yadong
Bie, Rongfang
Ren, Gang
author_facet Wu, Hao
Zhai, Xiaobo
Lei, Dongsheng
Liu, Jianfang
Yu, Yadong
Bie, Rongfang
Ren, Gang
author_sort Wu, Hao
collection PubMed
description Three-dimensional (3D) reconstruction of a single protein molecule is essential for understanding the relationship between the structural dynamics and functions of the protein. Electron tomography (ET) provides a tool for imaging an individual particle of protein from a series of tilted angles. Individual-particle electron tomography (IPET) provides an approach for reconstructing a 3D density map from a single targeted protein particle (without averaging from different particles of this type of protein), in which the target particle was imaged from a series of tilting angles. However, owing to radiation damage limitations, low-dose images (high noise, and low image contrast) are often challenging to be aligned for 3D reconstruction at intermediate resolution (1–3 nm). Here, we propose a computational method to enhance the image contrast, without increasing any experimental dose, for IPET 3D reconstruction. Using an edge-preserving smoothing-based multi-scale image decomposition algorithm, this method can detect the object against a high-noise background and enhance the object image contrast without increasing the noise level or significantly decreasing the image resolution. The method was validated by using both negative staining (NS) ET and cryo-ET images. The successful 3D reconstruction of a small molecule (<100 kDa) indicated that this method can be used as a supporting tool to current ET 3D reconstruction methods for studying protein dynamics via structure determination from each individual particle of the same type of protein.
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spelling pubmed-62320922018-11-28 An Algorithm for Enhancing the Image Contrast of Electron Tomography Wu, Hao Zhai, Xiaobo Lei, Dongsheng Liu, Jianfang Yu, Yadong Bie, Rongfang Ren, Gang Sci Rep Article Three-dimensional (3D) reconstruction of a single protein molecule is essential for understanding the relationship between the structural dynamics and functions of the protein. Electron tomography (ET) provides a tool for imaging an individual particle of protein from a series of tilted angles. Individual-particle electron tomography (IPET) provides an approach for reconstructing a 3D density map from a single targeted protein particle (without averaging from different particles of this type of protein), in which the target particle was imaged from a series of tilting angles. However, owing to radiation damage limitations, low-dose images (high noise, and low image contrast) are often challenging to be aligned for 3D reconstruction at intermediate resolution (1–3 nm). Here, we propose a computational method to enhance the image contrast, without increasing any experimental dose, for IPET 3D reconstruction. Using an edge-preserving smoothing-based multi-scale image decomposition algorithm, this method can detect the object against a high-noise background and enhance the object image contrast without increasing the noise level or significantly decreasing the image resolution. The method was validated by using both negative staining (NS) ET and cryo-ET images. The successful 3D reconstruction of a small molecule (<100 kDa) indicated that this method can be used as a supporting tool to current ET 3D reconstruction methods for studying protein dynamics via structure determination from each individual particle of the same type of protein. Nature Publishing Group UK 2018-11-12 /pmc/articles/PMC6232092/ /pubmed/30420636 http://dx.doi.org/10.1038/s41598-018-34652-9 Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Wu, Hao
Zhai, Xiaobo
Lei, Dongsheng
Liu, Jianfang
Yu, Yadong
Bie, Rongfang
Ren, Gang
An Algorithm for Enhancing the Image Contrast of Electron Tomography
title An Algorithm for Enhancing the Image Contrast of Electron Tomography
title_full An Algorithm for Enhancing the Image Contrast of Electron Tomography
title_fullStr An Algorithm for Enhancing the Image Contrast of Electron Tomography
title_full_unstemmed An Algorithm for Enhancing the Image Contrast of Electron Tomography
title_short An Algorithm for Enhancing the Image Contrast of Electron Tomography
title_sort algorithm for enhancing the image contrast of electron tomography
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6232092/
https://www.ncbi.nlm.nih.gov/pubmed/30420636
http://dx.doi.org/10.1038/s41598-018-34652-9
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