Chemical Mimicry: Hierarchical 1D TiO2@ZrO2 Core−Shell Structures Reminiscent of Sponge Spicules by the Synergistic Effect of Silicatein-α and Silintaphin-1
In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated b...
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Veröffentlicht in: | Langmuir 2011-05, Vol.27 (9), p.5464-5471 |
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creator | André, Rute Tahir, Muhammad Nawaz Link, Thorben Jochum, Florian D Kolb, Ute Theato, Patrick Berger, Rüdiger Wiens, Matthias Schröder, Heinz-Christoph Müller, Werner E. G Tremel, Wolfgang |
description | In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated by an axial proteinaceous filament with silicatein-α, one of the main components. But so far, the effect of other organic constituents from the proteinaceous filament on the catalytic effect of silicatein-α has not been studied in detail. Here we describe the synthesis of core−shell TiO2@SiO2 and TiO2@ZrO2 nanofibers via grafting of silicatein-α onto a TiO2 nanowire backbone followed by a coassembly of silintaphin-1 through its specifically interacting domains. We show for the first time a linker-free, one-step funtionalization of metal oxides with silicatein-α using glutamate tag. In the presence of silintaphin-1 silicatein-α facilitates the formation of a dense layer of SiO2 or ZrO2 on the TiO2@protein backbone template. The immobilization of silicatein-α onto TiO2 probes was characterized by atomic force microscopy (AFM), optical light microscopy, and high-resolution transmission electron microscopy (HRTEM). The coassembly of silicatein-α and silintaphin-1 may contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based biomaterials. |
doi_str_mv | 10.1021/la200066q |
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G ; Tremel, Wolfgang</creator><creatorcontrib>André, Rute ; Tahir, Muhammad Nawaz ; Link, Thorben ; Jochum, Florian D ; Kolb, Ute ; Theato, Patrick ; Berger, Rüdiger ; Wiens, Matthias ; Schröder, Heinz-Christoph ; Müller, Werner E. G ; Tremel, Wolfgang</creatorcontrib><description>In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated by an axial proteinaceous filament with silicatein-α, one of the main components. But so far, the effect of other organic constituents from the proteinaceous filament on the catalytic effect of silicatein-α has not been studied in detail. Here we describe the synthesis of core−shell TiO2@SiO2 and TiO2@ZrO2 nanofibers via grafting of silicatein-α onto a TiO2 nanowire backbone followed by a coassembly of silintaphin-1 through its specifically interacting domains. We show for the first time a linker-free, one-step funtionalization of metal oxides with silicatein-α using glutamate tag. In the presence of silintaphin-1 silicatein-α facilitates the formation of a dense layer of SiO2 or ZrO2 on the TiO2@protein backbone template. The immobilization of silicatein-α onto TiO2 probes was characterized by atomic force microscopy (AFM), optical light microscopy, and high-resolution transmission electron microscopy (HRTEM). The coassembly of silicatein-α and silintaphin-1 may contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based biomaterials.</description><identifier>ISSN: 0743-7463</identifier><identifier>EISSN: 1520-5827</identifier><identifier>DOI: 10.1021/la200066q</identifier><identifier>PMID: 21456536</identifier><identifier>CODEN: LANGD5</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Animals ; Biological Interfaces: Biocolloids, Biomolecular and Biomimetic Materials ; Biomimetic Materials - chemistry ; Catalysis ; Cathepsins - chemistry ; Chemistry ; Enzymes, Immobilized - chemistry ; Exact sciences and technology ; General and physical chemistry ; Glutamic Acid - chemistry ; Nanowires - chemistry ; Suberites - chemistry ; Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry ; Titanium - chemistry ; Zirconium - chemistry</subject><ispartof>Langmuir, 2011-05, Vol.27 (9), p.5464-5471</ispartof><rights>Copyright © 2011 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/la200066q$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/la200066q$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24117270$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21456536$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>André, Rute</creatorcontrib><creatorcontrib>Tahir, Muhammad Nawaz</creatorcontrib><creatorcontrib>Link, Thorben</creatorcontrib><creatorcontrib>Jochum, Florian D</creatorcontrib><creatorcontrib>Kolb, Ute</creatorcontrib><creatorcontrib>Theato, Patrick</creatorcontrib><creatorcontrib>Berger, Rüdiger</creatorcontrib><creatorcontrib>Wiens, Matthias</creatorcontrib><creatorcontrib>Schröder, Heinz-Christoph</creatorcontrib><creatorcontrib>Müller, Werner E. G</creatorcontrib><creatorcontrib>Tremel, Wolfgang</creatorcontrib><title>Chemical Mimicry: Hierarchical 1D TiO2@ZrO2 Core−Shell Structures Reminiscent of Sponge Spicules by the Synergistic Effect of Silicatein-α and Silintaphin-1</title><title>Langmuir</title><addtitle>Langmuir</addtitle><description>In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated by an axial proteinaceous filament with silicatein-α, one of the main components. But so far, the effect of other organic constituents from the proteinaceous filament on the catalytic effect of silicatein-α has not been studied in detail. Here we describe the synthesis of core−shell TiO2@SiO2 and TiO2@ZrO2 nanofibers via grafting of silicatein-α onto a TiO2 nanowire backbone followed by a coassembly of silintaphin-1 through its specifically interacting domains. We show for the first time a linker-free, one-step funtionalization of metal oxides with silicatein-α using glutamate tag. In the presence of silintaphin-1 silicatein-α facilitates the formation of a dense layer of SiO2 or ZrO2 on the TiO2@protein backbone template. The immobilization of silicatein-α onto TiO2 probes was characterized by atomic force microscopy (AFM), optical light microscopy, and high-resolution transmission electron microscopy (HRTEM). The coassembly of silicatein-α and silintaphin-1 may contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based biomaterials.</description><subject>Animals</subject><subject>Biological Interfaces: Biocolloids, Biomolecular and Biomimetic Materials</subject><subject>Biomimetic Materials - chemistry</subject><subject>Catalysis</subject><subject>Cathepsins - chemistry</subject><subject>Chemistry</subject><subject>Enzymes, Immobilized - chemistry</subject><subject>Exact sciences and technology</subject><subject>General and physical chemistry</subject><subject>Glutamic Acid - chemistry</subject><subject>Nanowires - chemistry</subject><subject>Suberites - chemistry</subject><subject>Theory of reactions, general kinetics. Catalysis. 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Nomenclature, chemical documentation, computer chemistry</topic><topic>Titanium - chemistry</topic><topic>Zirconium - chemistry</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>André, Rute</creatorcontrib><creatorcontrib>Tahir, Muhammad Nawaz</creatorcontrib><creatorcontrib>Link, Thorben</creatorcontrib><creatorcontrib>Jochum, Florian D</creatorcontrib><creatorcontrib>Kolb, Ute</creatorcontrib><creatorcontrib>Theato, Patrick</creatorcontrib><creatorcontrib>Berger, Rüdiger</creatorcontrib><creatorcontrib>Wiens, Matthias</creatorcontrib><creatorcontrib>Schröder, Heinz-Christoph</creatorcontrib><creatorcontrib>Müller, Werner E. 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G</au><au>Tremel, Wolfgang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Chemical Mimicry: Hierarchical 1D TiO2@ZrO2 Core−Shell Structures Reminiscent of Sponge Spicules by the Synergistic Effect of Silicatein-α and Silintaphin-1</atitle><jtitle>Langmuir</jtitle><addtitle>Langmuir</addtitle><date>2011-05-03</date><risdate>2011</risdate><volume>27</volume><issue>9</issue><spage>5464</spage><epage>5471</epage><pages>5464-5471</pages><issn>0743-7463</issn><eissn>1520-5827</eissn><coden>LANGD5</coden><abstract>In nature, mineralization of hard tissues occurs due to the synergistic effect of components present in the organic matrix of these tissues, with templating and catalytic effects. In Suberites domuncula, a well-studied example of the class of demosponges, silica formation is mediated and templated by an axial proteinaceous filament with silicatein-α, one of the main components. But so far, the effect of other organic constituents from the proteinaceous filament on the catalytic effect of silicatein-α has not been studied in detail. Here we describe the synthesis of core−shell TiO2@SiO2 and TiO2@ZrO2 nanofibers via grafting of silicatein-α onto a TiO2 nanowire backbone followed by a coassembly of silintaphin-1 through its specifically interacting domains. We show for the first time a linker-free, one-step funtionalization of metal oxides with silicatein-α using glutamate tag. In the presence of silintaphin-1 silicatein-α facilitates the formation of a dense layer of SiO2 or ZrO2 on the TiO2@protein backbone template. The immobilization of silicatein-α onto TiO2 probes was characterized by atomic force microscopy (AFM), optical light microscopy, and high-resolution transmission electron microscopy (HRTEM). The coassembly of silicatein-α and silintaphin-1 may contribute to biomimetic approaches that pursue a controlled formation of patterned biosilica-based biomaterials.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><pmid>21456536</pmid><doi>10.1021/la200066q</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Biological Interfaces: Biocolloids, Biomolecular and Biomimetic Materials Biomimetic Materials - chemistry Catalysis Cathepsins - chemistry Chemistry Enzymes, Immobilized - chemistry Exact sciences and technology General and physical chemistry Glutamic Acid - chemistry Nanowires - chemistry Suberites - chemistry Theory of reactions, general kinetics. Catalysis. Nomenclature, chemical documentation, computer chemistry Titanium - chemistry Zirconium - chemistry |
title | Chemical Mimicry: Hierarchical 1D TiO2@ZrO2 Core−Shell Structures Reminiscent of Sponge Spicules by the Synergistic Effect of Silicatein-α and Silintaphin-1 |
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