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Scanning electron microscope studies of human metaphase chromosomes

Scanning electron microscopy (SEM) is used to evaluate potential chromosome preparations and staining methods for application in high-resolution three-dimensional X-ray imaging. Our starting point is optical fluorescence microscopy, the standard method for chromosomes, which only gives structural de...

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Detalles Bibliográficos
Autores principales: Shemilt, L. A., Estandarte, A. K. C., Yusuf, M., Robinson, I. K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society Publishing 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900039/
https://www.ncbi.nlm.nih.gov/pubmed/24470422
http://dx.doi.org/10.1098/rsta.2013.0144
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author Shemilt, L. A.
Estandarte, A. K. C.
Yusuf, M.
Robinson, I. K.
author_facet Shemilt, L. A.
Estandarte, A. K. C.
Yusuf, M.
Robinson, I. K.
author_sort Shemilt, L. A.
collection PubMed
description Scanning electron microscopy (SEM) is used to evaluate potential chromosome preparations and staining methods for application in high-resolution three-dimensional X-ray imaging. Our starting point is optical fluorescence microscopy, the standard method for chromosomes, which only gives structural detail at the 200 nm scale. In principle, with suitable sample preparation protocols, including contrast enhancing staining, the surface structure of the chromosomes can be viewed at the 1 nm level by SEM. Here, we evaluate a heavy metal nucleic-acid-specific stain, which gives strong contrast in the backscattered electron signal. This study uses SEM to examine chromosomes prepared in different ways to establish a sample preparation protocol for X-rays. Secondary electron and backscattered electron signals are compared to evaluate the effectiveness of platinum-based stains used to enhance the contrast.
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spelling pubmed-39000392014-03-06 Scanning electron microscope studies of human metaphase chromosomes Shemilt, L. A. Estandarte, A. K. C. Yusuf, M. Robinson, I. K. Philos Trans A Math Phys Eng Sci Articles Scanning electron microscopy (SEM) is used to evaluate potential chromosome preparations and staining methods for application in high-resolution three-dimensional X-ray imaging. Our starting point is optical fluorescence microscopy, the standard method for chromosomes, which only gives structural detail at the 200 nm scale. In principle, with suitable sample preparation protocols, including contrast enhancing staining, the surface structure of the chromosomes can be viewed at the 1 nm level by SEM. Here, we evaluate a heavy metal nucleic-acid-specific stain, which gives strong contrast in the backscattered electron signal. This study uses SEM to examine chromosomes prepared in different ways to establish a sample preparation protocol for X-rays. Secondary electron and backscattered electron signals are compared to evaluate the effectiveness of platinum-based stains used to enhance the contrast. The Royal Society Publishing 2014-03-06 /pmc/articles/PMC3900039/ /pubmed/24470422 http://dx.doi.org/10.1098/rsta.2013.0144 Text en http://creativecommons.org/licenses/by/3.0/ © 2014 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/3.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Shemilt, L. A.
Estandarte, A. K. C.
Yusuf, M.
Robinson, I. K.
Scanning electron microscope studies of human metaphase chromosomes
title Scanning electron microscope studies of human metaphase chromosomes
title_full Scanning electron microscope studies of human metaphase chromosomes
title_fullStr Scanning electron microscope studies of human metaphase chromosomes
title_full_unstemmed Scanning electron microscope studies of human metaphase chromosomes
title_short Scanning electron microscope studies of human metaphase chromosomes
title_sort scanning electron microscope studies of human metaphase chromosomes
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900039/
https://www.ncbi.nlm.nih.gov/pubmed/24470422
http://dx.doi.org/10.1098/rsta.2013.0144
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