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Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira
High-resolution 3D images of organelles are of paramount importance in cellular biology. Although light microscopy and transmission electron microscopy (TEM) have provided the standard for imaging cellular structures, they cannot provide 3D images. However, recent technological advances such as seri...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750564/ https://www.ncbi.nlm.nih.gov/pubmed/35011629 http://dx.doi.org/10.3390/cells11010065 |
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author | Garza-Lopez, Edgar Vue, Zer Katti, Prasanna Neikirk, Kit Biete, Michelle Lam, Jacob Beasley, Heather K. Marshall, Andrea G. Rodman, Taylor A. Christensen, Trace A. Salisbury, Jeffrey L. Vang, Larry Mungai, Margaret AshShareef, Salma Murray, Sandra A. Shao, Jianqiang Streeter, Jennifer Glancy, Brian Pereira, Renata O. Abel, E. Dale Hinton, Antentor |
author_facet | Garza-Lopez, Edgar Vue, Zer Katti, Prasanna Neikirk, Kit Biete, Michelle Lam, Jacob Beasley, Heather K. Marshall, Andrea G. Rodman, Taylor A. Christensen, Trace A. Salisbury, Jeffrey L. Vang, Larry Mungai, Margaret AshShareef, Salma Murray, Sandra A. Shao, Jianqiang Streeter, Jennifer Glancy, Brian Pereira, Renata O. Abel, E. Dale Hinton, Antentor |
author_sort | Garza-Lopez, Edgar |
collection | PubMed |
description | High-resolution 3D images of organelles are of paramount importance in cellular biology. Although light microscopy and transmission electron microscopy (TEM) have provided the standard for imaging cellular structures, they cannot provide 3D images. However, recent technological advances such as serial block-face scanning electron microscopy (SBF-SEM) and focused ion beam scanning electron microscopy (FIB-SEM) provide the tools to create 3D images for the ultrastructural analysis of organelles. Here, we describe a standardized protocol using the visualization software, Amira, to quantify organelle morphologies in 3D, thereby providing accurate and reproducible measurements of these cellular substructures. We demonstrate applications of SBF-SEM and Amira to quantify mitochondria and endoplasmic reticulum (ER) structures. |
format | Online Article Text |
id | pubmed-8750564 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87505642022-01-12 Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira Garza-Lopez, Edgar Vue, Zer Katti, Prasanna Neikirk, Kit Biete, Michelle Lam, Jacob Beasley, Heather K. Marshall, Andrea G. Rodman, Taylor A. Christensen, Trace A. Salisbury, Jeffrey L. Vang, Larry Mungai, Margaret AshShareef, Salma Murray, Sandra A. Shao, Jianqiang Streeter, Jennifer Glancy, Brian Pereira, Renata O. Abel, E. Dale Hinton, Antentor Cells Article High-resolution 3D images of organelles are of paramount importance in cellular biology. Although light microscopy and transmission electron microscopy (TEM) have provided the standard for imaging cellular structures, they cannot provide 3D images. However, recent technological advances such as serial block-face scanning electron microscopy (SBF-SEM) and focused ion beam scanning electron microscopy (FIB-SEM) provide the tools to create 3D images for the ultrastructural analysis of organelles. Here, we describe a standardized protocol using the visualization software, Amira, to quantify organelle morphologies in 3D, thereby providing accurate and reproducible measurements of these cellular substructures. We demonstrate applications of SBF-SEM and Amira to quantify mitochondria and endoplasmic reticulum (ER) structures. MDPI 2021-12-27 /pmc/articles/PMC8750564/ /pubmed/35011629 http://dx.doi.org/10.3390/cells11010065 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Garza-Lopez, Edgar Vue, Zer Katti, Prasanna Neikirk, Kit Biete, Michelle Lam, Jacob Beasley, Heather K. Marshall, Andrea G. Rodman, Taylor A. Christensen, Trace A. Salisbury, Jeffrey L. Vang, Larry Mungai, Margaret AshShareef, Salma Murray, Sandra A. Shao, Jianqiang Streeter, Jennifer Glancy, Brian Pereira, Renata O. Abel, E. Dale Hinton, Antentor Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title | Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title_full | Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title_fullStr | Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title_full_unstemmed | Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title_short | Protocols for Generating Surfaces and Measuring 3D Organelle Morphology Using Amira |
title_sort | protocols for generating surfaces and measuring 3d organelle morphology using amira |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8750564/ https://www.ncbi.nlm.nih.gov/pubmed/35011629 http://dx.doi.org/10.3390/cells11010065 |
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