A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy
Observing cells and cell components in three dimensions at high magnification in transmission electron microscopy requires preparing serial ultrathin sections of the specimen. Although preparing serial ultrathin sections is considered to be very difficult, it is rather easy if the proper method is u...
Gespeichert in:
Veröffentlicht in: | Journal of Visualized Experiments 2018-01 (131) |
---|---|
Hauptverfasser: | , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext bestellen |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | |
---|---|
container_issue | 131 |
container_start_page | |
container_title | Journal of Visualized Experiments |
container_volume | |
creator | Yamaguchi, Masashi Chibana, Hiroji |
description | Observing cells and cell components in three dimensions at high magnification in transmission electron microscopy requires preparing serial ultrathin sections of the specimen. Although preparing serial ultrathin sections is considered to be very difficult, it is rather easy if the proper method is used. In this paper, we show a step-by-step procedure for safely obtaining serial ultrathin sections of microorganisms. The key points of this method are: 1) to use the large part of the specimen and adjust the specimen surface and knife edge so that they are parallel to each other; 2) to cut serial sections in groups and avoid difficulty in separating sections using a pair of hair strands when retrieving a group of serial sections onto the slit grids; 3) to use a 'Section-holding loop' and avoid mixing up the order of the section groups; 4) to use a 'Water-surface-raising loop' and make sure the sections are positioned on the apex of the water and that they touch the grid first, in order to place them in the desired position on the grids; 5) to use the support film on an aluminum rack and make it easier to recover the sections on the grids and to avoid wrinkling of the support film; and 6) to use a staining tube and avoid accidentally breaking the support films with tweezers. This new method enables obtaining serial ultrathin sections without difficulty. The method makes it possible to analyze cell structures of microorganisms at high resolution in 3D, which cannot be achieved by using the automatic tape-collecting ultramicrotome method and serial block-face or focused ion beam scanning electron microscopy. |
doi_str_mv | 10.3791/56235 |
format | Article |
fullrecord | <record><control><sourceid>proquest_223</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5908661</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1990855236</sourcerecordid><originalsourceid>FETCH-LOGICAL-c448t-d3e7fa81a02eeebb97a219d07401c9960335184c71ca6b588eb82c2a146da1b03</originalsourceid><addsrcrecordid>eNpVkctqAjEUhkNpqdb6Al2UbArd2CaZmUyyKYjYCyguqtBdyGQyGhkTm4wF377xUrGrHHK-85_LD0AXo6ck5_g5oyTJLkAb8xT1EMu_Ls_iFrgJYYkQJShj16BFeEJTQtI2qPpwrJuFK2HlPJwUjTTW2Dn81N7IGs7qxstmYWz8UI1xNkBXwbFR3jk_l9aEVYAxO_XShpUJISJwWEfWx2DPBeXW21twVck66O7x7YDZ63A6eO-NJm8fg_6op9KUNb0y0XklGZaIaK2LgueSYF6iPEVYcU5RkmSYpSrHStIiY0wXjCgicUpLiQuUdMDLQXe9KVa6VNrG-Wux9mYl_VY4acT_jDULMXc_IuOIUYqjwONRwLvvjQ6NiFspXdfSarcJAvMIZhlJaEQfDuhuyeB1dWqDkdh5IvaeRO7-fKYT9WdCBO4OwNL9aLF0G2_jjY7VvwV0kUk</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1990855236</pqid></control><display><type>article</type><title>A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy</title><source>Journal of Visualized Experiments : JoVE</source><creator>Yamaguchi, Masashi ; Chibana, Hiroji</creator><creatorcontrib>Yamaguchi, Masashi ; Chibana, Hiroji</creatorcontrib><description>Observing cells and cell components in three dimensions at high magnification in transmission electron microscopy requires preparing serial ultrathin sections of the specimen. Although preparing serial ultrathin sections is considered to be very difficult, it is rather easy if the proper method is used. In this paper, we show a step-by-step procedure for safely obtaining serial ultrathin sections of microorganisms. The key points of this method are: 1) to use the large part of the specimen and adjust the specimen surface and knife edge so that they are parallel to each other; 2) to cut serial sections in groups and avoid difficulty in separating sections using a pair of hair strands when retrieving a group of serial sections onto the slit grids; 3) to use a 'Section-holding loop' and avoid mixing up the order of the section groups; 4) to use a 'Water-surface-raising loop' and make sure the sections are positioned on the apex of the water and that they touch the grid first, in order to place them in the desired position on the grids; 5) to use the support film on an aluminum rack and make it easier to recover the sections on the grids and to avoid wrinkling of the support film; and 6) to use a staining tube and avoid accidentally breaking the support films with tweezers. This new method enables obtaining serial ultrathin sections without difficulty. The method makes it possible to analyze cell structures of microorganisms at high resolution in 3D, which cannot be achieved by using the automatic tape-collecting ultramicrotome method and serial block-face or focused ion beam scanning electron microscopy.</description><identifier>ISSN: 1940-087X</identifier><identifier>EISSN: 1940-087X</identifier><identifier>DOI: 10.3791/56235</identifier><identifier>PMID: 29364224</identifier><language>eng</language><publisher>United States: MyJove Corporation</publisher><subject>Engineering ; Eukaryota - ultrastructure ; Histological Techniques - instrumentation ; Histological Techniques - methods ; Microscopy, Electron, Transmission - instrumentation ; Microscopy, Electron, Transmission - methods ; Microtomy - instrumentation ; Microtomy - methods ; Prokaryotic Cells - ultrastructure</subject><ispartof>Journal of Visualized Experiments, 2018-01 (131)</ispartof><rights>Copyright © 2018, Journal of Visualized Experiments</rights><rights>Copyright © 2018, Journal of Visualized Experiments 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-d3e7fa81a02eeebb97a219d07401c9960335184c71ca6b588eb82c2a146da1b03</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttps://www.jove.com/files/email_thumbs/56235.png</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908661/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5908661/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,3842,27923,27924,53790,53792</link.rule.ids><linktorsrc>$$Uhttp://dx.doi.org/10.3791/56235$$EView_record_in_Journal_of_Visualized_Experiments$$FView_record_in_$$GJournal_of_Visualized_Experiments</linktorsrc><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29364224$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yamaguchi, Masashi</creatorcontrib><creatorcontrib>Chibana, Hiroji</creatorcontrib><title>A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy</title><title>Journal of Visualized Experiments</title><addtitle>J Vis Exp</addtitle><description>Observing cells and cell components in three dimensions at high magnification in transmission electron microscopy requires preparing serial ultrathin sections of the specimen. Although preparing serial ultrathin sections is considered to be very difficult, it is rather easy if the proper method is used. In this paper, we show a step-by-step procedure for safely obtaining serial ultrathin sections of microorganisms. The key points of this method are: 1) to use the large part of the specimen and adjust the specimen surface and knife edge so that they are parallel to each other; 2) to cut serial sections in groups and avoid difficulty in separating sections using a pair of hair strands when retrieving a group of serial sections onto the slit grids; 3) to use a 'Section-holding loop' and avoid mixing up the order of the section groups; 4) to use a 'Water-surface-raising loop' and make sure the sections are positioned on the apex of the water and that they touch the grid first, in order to place them in the desired position on the grids; 5) to use the support film on an aluminum rack and make it easier to recover the sections on the grids and to avoid wrinkling of the support film; and 6) to use a staining tube and avoid accidentally breaking the support films with tweezers. This new method enables obtaining serial ultrathin sections without difficulty. The method makes it possible to analyze cell structures of microorganisms at high resolution in 3D, which cannot be achieved by using the automatic tape-collecting ultramicrotome method and serial block-face or focused ion beam scanning electron microscopy.</description><subject>Engineering</subject><subject>Eukaryota - ultrastructure</subject><subject>Histological Techniques - instrumentation</subject><subject>Histological Techniques - methods</subject><subject>Microscopy, Electron, Transmission - instrumentation</subject><subject>Microscopy, Electron, Transmission - methods</subject><subject>Microtomy - instrumentation</subject><subject>Microtomy - methods</subject><subject>Prokaryotic Cells - ultrastructure</subject><issn>1940-087X</issn><issn>1940-087X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkctqAjEUhkNpqdb6Al2UbArd2CaZmUyyKYjYCyguqtBdyGQyGhkTm4wF377xUrGrHHK-85_LD0AXo6ck5_g5oyTJLkAb8xT1EMu_Ls_iFrgJYYkQJShj16BFeEJTQtI2qPpwrJuFK2HlPJwUjTTW2Dn81N7IGs7qxstmYWz8UI1xNkBXwbFR3jk_l9aEVYAxO_XShpUJISJwWEfWx2DPBeXW21twVck66O7x7YDZ63A6eO-NJm8fg_6op9KUNb0y0XklGZaIaK2LgueSYF6iPEVYcU5RkmSYpSrHStIiY0wXjCgicUpLiQuUdMDLQXe9KVa6VNrG-Wux9mYl_VY4acT_jDULMXc_IuOIUYqjwONRwLvvjQ6NiFspXdfSarcJAvMIZhlJaEQfDuhuyeB1dWqDkdh5IvaeRO7-fKYT9WdCBO4OwNL9aLF0G2_jjY7VvwV0kUk</recordid><startdate>20180117</startdate><enddate>20180117</enddate><creator>Yamaguchi, Masashi</creator><creator>Chibana, Hiroji</creator><general>MyJove Corporation</general><scope>BHQUO</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20180117</creationdate><title>A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy</title><author>Yamaguchi, Masashi ; Chibana, Hiroji</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-d3e7fa81a02eeebb97a219d07401c9960335184c71ca6b588eb82c2a146da1b03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Engineering</topic><topic>Eukaryota - ultrastructure</topic><topic>Histological Techniques - instrumentation</topic><topic>Histological Techniques - methods</topic><topic>Microscopy, Electron, Transmission - instrumentation</topic><topic>Microscopy, Electron, Transmission - methods</topic><topic>Microtomy - instrumentation</topic><topic>Microtomy - methods</topic><topic>Prokaryotic Cells - ultrastructure</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yamaguchi, Masashi</creatorcontrib><creatorcontrib>Chibana, Hiroji</creatorcontrib><collection>JoVE Journal: Engineering</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of Visualized Experiments</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>Yamaguchi, Masashi</au><au>Chibana, Hiroji</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy</atitle><jtitle>Journal of Visualized Experiments</jtitle><addtitle>J Vis Exp</addtitle><date>2018-01-17</date><risdate>2018</risdate><issue>131</issue><issn>1940-087X</issn><eissn>1940-087X</eissn><abstract>Observing cells and cell components in three dimensions at high magnification in transmission electron microscopy requires preparing serial ultrathin sections of the specimen. Although preparing serial ultrathin sections is considered to be very difficult, it is rather easy if the proper method is used. In this paper, we show a step-by-step procedure for safely obtaining serial ultrathin sections of microorganisms. The key points of this method are: 1) to use the large part of the specimen and adjust the specimen surface and knife edge so that they are parallel to each other; 2) to cut serial sections in groups and avoid difficulty in separating sections using a pair of hair strands when retrieving a group of serial sections onto the slit grids; 3) to use a 'Section-holding loop' and avoid mixing up the order of the section groups; 4) to use a 'Water-surface-raising loop' and make sure the sections are positioned on the apex of the water and that they touch the grid first, in order to place them in the desired position on the grids; 5) to use the support film on an aluminum rack and make it easier to recover the sections on the grids and to avoid wrinkling of the support film; and 6) to use a staining tube and avoid accidentally breaking the support films with tweezers. This new method enables obtaining serial ultrathin sections without difficulty. The method makes it possible to analyze cell structures of microorganisms at high resolution in 3D, which cannot be achieved by using the automatic tape-collecting ultramicrotome method and serial block-face or focused ion beam scanning electron microscopy.</abstract><cop>United States</cop><pub>MyJove Corporation</pub><pmid>29364224</pmid><doi>10.3791/56235</doi><oa>free_for_read</oa></addata></record> |
fulltext | fulltext_linktorsrc |
identifier | ISSN: 1940-087X |
ispartof | Journal of Visualized Experiments, 2018-01 (131) |
issn | 1940-087X 1940-087X |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5908661 |
source | Journal of Visualized Experiments : JoVE |
subjects | Engineering Eukaryota - ultrastructure Histological Techniques - instrumentation Histological Techniques - methods Microscopy, Electron, Transmission - instrumentation Microscopy, Electron, Transmission - methods Microtomy - instrumentation Microtomy - methods Prokaryotic Cells - ultrastructure |
title | A Method for Obtaining Serial Ultrathin Sections of Microorganisms in Transmission Electron Microscopy |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-08T19%3A36%3A14IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_223&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A%20Method%20for%20Obtaining%20Serial%20Ultrathin%20Sections%20of%20Microorganisms%20in%20Transmission%20Electron%20Microscopy&rft.jtitle=Journal%20of%20Visualized%20Experiments&rft.au=Yamaguchi,%20Masashi&rft.date=2018-01-17&rft.issue=131&rft.issn=1940-087X&rft.eissn=1940-087X&rft_id=info:doi/10.3791/56235&rft_dat=%3Cproquest_223%3E1990855236%3C/proquest_223%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1990855236&rft_id=info:pmid/29364224&rfr_iscdi=true |