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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
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.
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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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