Diffraction Contrast Imaging of Extracellular Matrix Components Using Zero-Loss Filtering
The β-chitin microfibrils from the deep-sea hydrothermal vent wormRiftia pachyptilawere studied in both mature and fresh tubes experimentally obtained. The methods used were electron diffraction and electron diffraction contrast images, in conjunction with an electron-energy filter, operated in the...
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Veröffentlicht in: | Journal of structural biology 1997-10, Vol.120 (1), p.85-92 |
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description | The β-chitin microfibrils from the deep-sea hydrothermal vent wormRiftia pachyptilawere studied in both mature and fresh tubes experimentally obtained. The methods used were electron diffraction and electron diffraction contrast images, in conjunction with an electron-energy filter, operated in the zero-loss mode. In both studied samples, microfibrils are organized in successive layers, inside which they are parallel. However, the fresh tube is less densely packed and diffraction data show that these microfibrils may be in a partially hydrated state. These results indicate that a later step occurs in the compaction of the tube material once it has been extruded. Comparison of filtered and unfiltered diffraction patterns shows that zero-loss filtering significantly improves both working conditions and quality of diffraction recordings. |
doi_str_mv | 10.1006/jsbi.1997.3909 |
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The methods used were electron diffraction and electron diffraction contrast images, in conjunction with an electron-energy filter, operated in the zero-loss mode. In both studied samples, microfibrils are organized in successive layers, inside which they are parallel. However, the fresh tube is less densely packed and diffraction data show that these microfibrils may be in a partially hydrated state. These results indicate that a later step occurs in the compaction of the tube material once it has been extruded. Comparison of filtered and unfiltered diffraction patterns shows that zero-loss filtering significantly improves both working conditions and quality of diffraction recordings.</description><identifier>ISSN: 1047-8477</identifier><identifier>EISSN: 1095-8657</identifier><identifier>DOI: 10.1006/jsbi.1997.3909</identifier><identifier>PMID: 9356296</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Actin Cytoskeleton - ultrastructure ; Animals ; Chitin - ultrastructure ; Equipment Design ; Extracellular Matrix - chemistry ; Extracellular Matrix - ultrastructure ; Image Processing, Computer-Assisted ; Microscopy, Electron - instrumentation ; Microscopy, Electron - methods ; Models, Structural ; Polychaeta - physiology ; Polychaeta - ultrastructure ; Seawater</subject><ispartof>Journal of structural biology, 1997-10, Vol.120 (1), p.85-92</ispartof><rights>1997 Academic Press</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-254afac930bbf63c99aac370174723047a30516ef84b310cecdbd1c89383ac163</citedby><cites>FETCH-LOGICAL-c405t-254afac930bbf63c99aac370174723047a30516ef84b310cecdbd1c89383ac163</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1006/jsbi.1997.3909$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9356296$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Shillito, Bruce</creatorcontrib><creatorcontrib>Lechaire, Jean Pierre</creatorcontrib><creatorcontrib>Childress, Jim</creatorcontrib><creatorcontrib>Gaill, Françoise</creatorcontrib><title>Diffraction Contrast Imaging of Extracellular Matrix Components Using Zero-Loss Filtering</title><title>Journal of structural biology</title><addtitle>J Struct Biol</addtitle><description>The β-chitin microfibrils from the deep-sea hydrothermal vent wormRiftia pachyptilawere studied in both mature and fresh tubes experimentally obtained. The methods used were electron diffraction and electron diffraction contrast images, in conjunction with an electron-energy filter, operated in the zero-loss mode. In both studied samples, microfibrils are organized in successive layers, inside which they are parallel. However, the fresh tube is less densely packed and diffraction data show that these microfibrils may be in a partially hydrated state. These results indicate that a later step occurs in the compaction of the tube material once it has been extruded. Comparison of filtered and unfiltered diffraction patterns shows that zero-loss filtering significantly improves both working conditions and quality of diffraction recordings.</description><subject>Actin Cytoskeleton - ultrastructure</subject><subject>Animals</subject><subject>Chitin - ultrastructure</subject><subject>Equipment Design</subject><subject>Extracellular Matrix - chemistry</subject><subject>Extracellular Matrix - ultrastructure</subject><subject>Image Processing, Computer-Assisted</subject><subject>Microscopy, Electron - instrumentation</subject><subject>Microscopy, Electron - methods</subject><subject>Models, Structural</subject><subject>Polychaeta - physiology</subject><subject>Polychaeta - ultrastructure</subject><subject>Seawater</subject><issn>1047-8477</issn><issn>1095-8657</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kEFPwyAYhonRzDm9ejPpyVsrlBbK0cxNl8x4cQe9EEphYWnLBGrmv5dmizdPkO97ePPyAHCLYIYgJA87X5sMMUYzzCA7A1MEWZlWpKTn472gaVVQegmuvN9BCAuUowmYMFySnJEp-HgyWjshg7F9Mrd9cMKHZNWJrem3idXJ4hBHUrXt0AqXvIrgzCGC3d72qg8-2fgR_FTOpmvrfbI0bVAuzq7BhRatVzencwY2y8X7_CVdvz2v5o_rVBawDGleFkILyTCsa02wZEwIiSlEtKA5jv0FhiUiSldFjRGUSjZ1g2TFcIWFRATPwP0xd-_s16B84J3xY2HRKzt4ThlmhOZlBLMjKF0s6pTme2c64X44gnx0yUeXfHTJR5fxwd0peag71fzhJ3lxXx33Kn7v2yjHvTSql6oxTsnAG2v-i_4Fs2aD_g</recordid><startdate>199710</startdate><enddate>199710</enddate><creator>Shillito, Bruce</creator><creator>Lechaire, Jean Pierre</creator><creator>Childress, Jim</creator><creator>Gaill, Françoise</creator><general>Elsevier Inc</general><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></search><sort><creationdate>199710</creationdate><title>Diffraction Contrast Imaging of Extracellular Matrix Components Using Zero-Loss Filtering</title><author>Shillito, Bruce ; Lechaire, Jean Pierre ; Childress, Jim ; Gaill, Françoise</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c405t-254afac930bbf63c99aac370174723047a30516ef84b310cecdbd1c89383ac163</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Actin Cytoskeleton - ultrastructure</topic><topic>Animals</topic><topic>Chitin - ultrastructure</topic><topic>Equipment Design</topic><topic>Extracellular Matrix - chemistry</topic><topic>Extracellular Matrix - ultrastructure</topic><topic>Image Processing, Computer-Assisted</topic><topic>Microscopy, Electron - instrumentation</topic><topic>Microscopy, Electron - methods</topic><topic>Models, Structural</topic><topic>Polychaeta - physiology</topic><topic>Polychaeta - ultrastructure</topic><topic>Seawater</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Shillito, Bruce</creatorcontrib><creatorcontrib>Lechaire, Jean Pierre</creatorcontrib><creatorcontrib>Childress, Jim</creatorcontrib><creatorcontrib>Gaill, Françoise</creatorcontrib><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><jtitle>Journal of structural biology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Shillito, Bruce</au><au>Lechaire, Jean Pierre</au><au>Childress, Jim</au><au>Gaill, Françoise</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diffraction Contrast Imaging of Extracellular Matrix Components Using Zero-Loss Filtering</atitle><jtitle>Journal of structural biology</jtitle><addtitle>J Struct Biol</addtitle><date>1997-10</date><risdate>1997</risdate><volume>120</volume><issue>1</issue><spage>85</spage><epage>92</epage><pages>85-92</pages><issn>1047-8477</issn><eissn>1095-8657</eissn><abstract>The β-chitin microfibrils from the deep-sea hydrothermal vent wormRiftia pachyptilawere studied in both mature and fresh tubes experimentally obtained. The methods used were electron diffraction and electron diffraction contrast images, in conjunction with an electron-energy filter, operated in the zero-loss mode. In both studied samples, microfibrils are organized in successive layers, inside which they are parallel. However, the fresh tube is less densely packed and diffraction data show that these microfibrils may be in a partially hydrated state. These results indicate that a later step occurs in the compaction of the tube material once it has been extruded. Comparison of filtered and unfiltered diffraction patterns shows that zero-loss filtering significantly improves both working conditions and quality of diffraction recordings.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>9356296</pmid><doi>10.1006/jsbi.1997.3909</doi><tpages>8</tpages></addata></record> |
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subjects | Actin Cytoskeleton - ultrastructure Animals Chitin - ultrastructure Equipment Design Extracellular Matrix - chemistry Extracellular Matrix - ultrastructure Image Processing, Computer-Assisted Microscopy, Electron - instrumentation Microscopy, Electron - methods Models, Structural Polychaeta - physiology Polychaeta - ultrastructure Seawater |
title | Diffraction Contrast Imaging of Extracellular Matrix Components Using Zero-Loss Filtering |
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