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Self-assembly of regenerated silk fibroin from random coil nanostructures to antiparallel β-sheet nanostructures
ABSTRACT In this work, we studied the effects of incubation concentration and time on the self‐assembly behaviors of regenerated silk fibroin (RSF). Our results showed the assembly ways of RSF were concentration‐dependent and there were four self‐assembly ways of RSF: (i) At relatively low concentra...
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Published in: | Biopolymers 2014-12, Vol.101 (12), p.1181-1192 |
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creator | Zhong, Jian Ma, Mengjia Li, Wenying Zhou, Juan Yan, Zhiqiang He, Dannong |
description | ABSTRACT
In this work, we studied the effects of incubation concentration and time on the self‐assembly behaviors of regenerated silk fibroin (RSF). Our results showed the assembly ways of RSF were concentration‐dependent and there were four self‐assembly ways of RSF: (i) At relatively low concentration (≤0.015%), RSF molecules assembled into protofilaments (random coil), and then the thickness decreased and the secondary conformation changed to antiparallel β‐sheet; (ii) at the concentration of 0.015%, RSF molecules assembled into protofilaments (random coil), and then assembled into protofibrils (antiparallel β‐sheet). The protofibrils experienced the appearance and disappearance of phase periodic intervals in turn; (iii) at the concentration of 0.03%, RSF molecules assembled into bead‐like oligomers (random coil), and then assembled into protofibrils (antiparallel β‐sheet), and finally the height and phase periodic intervals of RSF protofibrils disappeared in turn; and (iv) at the relatively high concentration (≥0.15%), RSF molecules assembled into protofilaments (random coil), then aggregated into blurry cuboid‐like micelles (random coil), and finally self‐arranged to form smooth and clear cuboid‐like micelles (antiparallel β‐sheet). These results provide useful insights into the process by which the RSF molecules self‐assemble into protofilaments, protofibrils and micelles. Furthermore, our work will be beneficial to basic understanding of the nanoscale structure formations in different silk‐based biomaterials. © 2014 Wiley Periodicals, Inc. Biopolymers 101: 1181–1192, 2014. |
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In this work, we studied the effects of incubation concentration and time on the self‐assembly behaviors of regenerated silk fibroin (RSF). Our results showed the assembly ways of RSF were concentration‐dependent and there were four self‐assembly ways of RSF: (i) At relatively low concentration (≤0.015%), RSF molecules assembled into protofilaments (random coil), and then the thickness decreased and the secondary conformation changed to antiparallel β‐sheet; (ii) at the concentration of 0.015%, RSF molecules assembled into protofilaments (random coil), and then assembled into protofibrils (antiparallel β‐sheet). The protofibrils experienced the appearance and disappearance of phase periodic intervals in turn; (iii) at the concentration of 0.03%, RSF molecules assembled into bead‐like oligomers (random coil), and then assembled into protofibrils (antiparallel β‐sheet), and finally the height and phase periodic intervals of RSF protofibrils disappeared in turn; and (iv) at the relatively high concentration (≥0.15%), RSF molecules assembled into protofilaments (random coil), then aggregated into blurry cuboid‐like micelles (random coil), and finally self‐arranged to form smooth and clear cuboid‐like micelles (antiparallel β‐sheet). These results provide useful insights into the process by which the RSF molecules self‐assemble into protofilaments, protofibrils and micelles. Furthermore, our work will be beneficial to basic understanding of the nanoscale structure formations in different silk‐based biomaterials. © 2014 Wiley Periodicals, Inc. Biopolymers 101: 1181–1192, 2014.</description><identifier>ISSN: 0006-3525</identifier><identifier>EISSN: 1097-0282</identifier><identifier>DOI: 10.1002/bip.22532</identifier><identifier>PMID: 25088327</identifier><language>eng</language><publisher>United States: Blackwell Publishing Ltd</publisher><subject>Animals ; atomic force microscopy ; Biomedical materials ; Biopolymers ; Bombyx ; Circular Dichroism ; Coiling ; Fibroins - chemistry ; Fibroins - ultrastructure ; Intervals ; micelle ; Micelles ; Microscopy, Atomic Force ; Models, Molecular ; molecular self-assembly ; Nanostructure ; Nanostructures - chemistry ; Nanostructures - ultrastructure ; Protein Structure, Secondary ; protofibril ; protofilament ; Self assembly ; Silk fibroin ; Spectroscopy, Fourier Transform Infrared ; Temperature</subject><ispartof>Biopolymers, 2014-12, Vol.101 (12), p.1181-1192</ispartof><rights>2014 Wiley Periodicals, Inc.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4642-49b539bcc55f70b47855d26d0303bda93189706af65848d077b053ce1dcbaee83</citedby><cites>FETCH-LOGICAL-c4642-49b539bcc55f70b47855d26d0303bda93189706af65848d077b053ce1dcbaee83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25088327$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhong, Jian</creatorcontrib><creatorcontrib>Ma, Mengjia</creatorcontrib><creatorcontrib>Li, Wenying</creatorcontrib><creatorcontrib>Zhou, Juan</creatorcontrib><creatorcontrib>Yan, Zhiqiang</creatorcontrib><creatorcontrib>He, Dannong</creatorcontrib><title>Self-assembly of regenerated silk fibroin from random coil nanostructures to antiparallel β-sheet nanostructures</title><title>Biopolymers</title><addtitle>Biopolymers</addtitle><description>ABSTRACT
In this work, we studied the effects of incubation concentration and time on the self‐assembly behaviors of regenerated silk fibroin (RSF). Our results showed the assembly ways of RSF were concentration‐dependent and there were four self‐assembly ways of RSF: (i) At relatively low concentration (≤0.015%), RSF molecules assembled into protofilaments (random coil), and then the thickness decreased and the secondary conformation changed to antiparallel β‐sheet; (ii) at the concentration of 0.015%, RSF molecules assembled into protofilaments (random coil), and then assembled into protofibrils (antiparallel β‐sheet). The protofibrils experienced the appearance and disappearance of phase periodic intervals in turn; (iii) at the concentration of 0.03%, RSF molecules assembled into bead‐like oligomers (random coil), and then assembled into protofibrils (antiparallel β‐sheet), and finally the height and phase periodic intervals of RSF protofibrils disappeared in turn; and (iv) at the relatively high concentration (≥0.15%), RSF molecules assembled into protofilaments (random coil), then aggregated into blurry cuboid‐like micelles (random coil), and finally self‐arranged to form smooth and clear cuboid‐like micelles (antiparallel β‐sheet). These results provide useful insights into the process by which the RSF molecules self‐assemble into protofilaments, protofibrils and micelles. Furthermore, our work will be beneficial to basic understanding of the nanoscale structure formations in different silk‐based biomaterials. © 2014 Wiley Periodicals, Inc. Biopolymers 101: 1181–1192, 2014.</description><subject>Animals</subject><subject>atomic force microscopy</subject><subject>Biomedical materials</subject><subject>Biopolymers</subject><subject>Bombyx</subject><subject>Circular Dichroism</subject><subject>Coiling</subject><subject>Fibroins - chemistry</subject><subject>Fibroins - ultrastructure</subject><subject>Intervals</subject><subject>micelle</subject><subject>Micelles</subject><subject>Microscopy, Atomic Force</subject><subject>Models, Molecular</subject><subject>molecular self-assembly</subject><subject>Nanostructure</subject><subject>Nanostructures - chemistry</subject><subject>Nanostructures - ultrastructure</subject><subject>Protein Structure, Secondary</subject><subject>protofibril</subject><subject>protofilament</subject><subject>Self assembly</subject><subject>Silk fibroin</subject><subject>Spectroscopy, Fourier Transform Infrared</subject><subject>Temperature</subject><issn>0006-3525</issn><issn>1097-0282</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><recordid>eNqFkcFu1TAQRS0Eoq-FBT-AvIRF2rEd28kSCi2tKkCiCImNZTsTMHXiVzsRvN_qh_BNpH1tF0iI1d2ce0aaS8gzBvsMgB-4sN7nXAr-gKwYtLoC3vCHZAUAqhKSyx2yW8oPgLoWDB6THS6haQTXK3L5CWNf2VJwcHFDU08zfsMRs52woyXEC9oHl1MYaZ_TQLMduyV8CpGOdkxlyrOf5oyFTonacQprm22MGOnvq6p8R5z-4p6QR72NBZ_e5h75fPT2_PBddfbh-OTw1Vnla1Xzqm6dFK3zXspeg6t1I2XHVQcChOtsK1jTalC2V7Kpmw60diCFR9Z5ZxEbsUdebL3rnC5nLJMZQvEYox0xzcUwpZlctEL8H5VKLefbli_oyy3qcyolY2_WOQw2bwwDcz2GWcYwN2Ms7PNb7ewG7O7Ju-8vwMEW-Bkibv5tMq9PPt4pq20jlAl_3TdsvjBKCy3Nl_fHhr05P4XmqzSt-APL-qSD</recordid><startdate>201412</startdate><enddate>201412</enddate><creator>Zhong, Jian</creator><creator>Ma, Mengjia</creator><creator>Li, Wenying</creator><creator>Zhou, Juan</creator><creator>Yan, Zhiqiang</creator><creator>He, Dannong</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7QO</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7U5</scope><scope>L7M</scope></search><sort><creationdate>201412</creationdate><title>Self-assembly of regenerated silk fibroin from random coil nanostructures to antiparallel β-sheet nanostructures</title><author>Zhong, Jian ; Ma, Mengjia ; Li, Wenying ; Zhou, Juan ; Yan, Zhiqiang ; He, Dannong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4642-49b539bcc55f70b47855d26d0303bda93189706af65848d077b053ce1dcbaee83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Animals</topic><topic>atomic force microscopy</topic><topic>Biomedical materials</topic><topic>Biopolymers</topic><topic>Bombyx</topic><topic>Circular Dichroism</topic><topic>Coiling</topic><topic>Fibroins - chemistry</topic><topic>Fibroins - ultrastructure</topic><topic>Intervals</topic><topic>micelle</topic><topic>Micelles</topic><topic>Microscopy, Atomic Force</topic><topic>Models, Molecular</topic><topic>molecular self-assembly</topic><topic>Nanostructure</topic><topic>Nanostructures - chemistry</topic><topic>Nanostructures - ultrastructure</topic><topic>Protein Structure, Secondary</topic><topic>protofibril</topic><topic>protofilament</topic><topic>Self assembly</topic><topic>Silk fibroin</topic><topic>Spectroscopy, Fourier Transform Infrared</topic><topic>Temperature</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhong, Jian</creatorcontrib><creatorcontrib>Ma, Mengjia</creatorcontrib><creatorcontrib>Li, Wenying</creatorcontrib><creatorcontrib>Zhou, Juan</creatorcontrib><creatorcontrib>Yan, Zhiqiang</creatorcontrib><creatorcontrib>He, Dannong</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Biopolymers</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhong, Jian</au><au>Ma, Mengjia</au><au>Li, Wenying</au><au>Zhou, Juan</au><au>Yan, Zhiqiang</au><au>He, Dannong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Self-assembly of regenerated silk fibroin from random coil nanostructures to antiparallel β-sheet nanostructures</atitle><jtitle>Biopolymers</jtitle><addtitle>Biopolymers</addtitle><date>2014-12</date><risdate>2014</risdate><volume>101</volume><issue>12</issue><spage>1181</spage><epage>1192</epage><pages>1181-1192</pages><issn>0006-3525</issn><eissn>1097-0282</eissn><abstract>ABSTRACT
In this work, we studied the effects of incubation concentration and time on the self‐assembly behaviors of regenerated silk fibroin (RSF). Our results showed the assembly ways of RSF were concentration‐dependent and there were four self‐assembly ways of RSF: (i) At relatively low concentration (≤0.015%), RSF molecules assembled into protofilaments (random coil), and then the thickness decreased and the secondary conformation changed to antiparallel β‐sheet; (ii) at the concentration of 0.015%, RSF molecules assembled into protofilaments (random coil), and then assembled into protofibrils (antiparallel β‐sheet). The protofibrils experienced the appearance and disappearance of phase periodic intervals in turn; (iii) at the concentration of 0.03%, RSF molecules assembled into bead‐like oligomers (random coil), and then assembled into protofibrils (antiparallel β‐sheet), and finally the height and phase periodic intervals of RSF protofibrils disappeared in turn; and (iv) at the relatively high concentration (≥0.15%), RSF molecules assembled into protofilaments (random coil), then aggregated into blurry cuboid‐like micelles (random coil), and finally self‐arranged to form smooth and clear cuboid‐like micelles (antiparallel β‐sheet). These results provide useful insights into the process by which the RSF molecules self‐assemble into protofilaments, protofibrils and micelles. Furthermore, our work will be beneficial to basic understanding of the nanoscale structure formations in different silk‐based biomaterials. © 2014 Wiley Periodicals, Inc. Biopolymers 101: 1181–1192, 2014.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>25088327</pmid><doi>10.1002/bip.22532</doi><tpages>12</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals atomic force microscopy Biomedical materials Biopolymers Bombyx Circular Dichroism Coiling Fibroins - chemistry Fibroins - ultrastructure Intervals micelle Micelles Microscopy, Atomic Force Models, Molecular molecular self-assembly Nanostructure Nanostructures - chemistry Nanostructures - ultrastructure Protein Structure, Secondary protofibril protofilament Self assembly Silk fibroin Spectroscopy, Fourier Transform Infrared Temperature |
title | Self-assembly of regenerated silk fibroin from random coil nanostructures to antiparallel β-sheet nanostructures |
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