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Conference Paper: Profiling biomolecules at cell-biomaterial interface by quantitative proteomics
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TitleProfiling biomolecules at cell-biomaterial interface by quantitative proteomics
 
AuthorsTong, WY
Liang, YM
Tam, V
Yip, HK
Kao, YT
Cheung, KMC
Yeung, KWK
Lam, YW
 
Issue Date2010
 
PublisherTERMIS-NA.
 
CitationThe 2010 North America Conference of the Tissue Engineering and Regenerative Medicine International Society (TERMIS-NA 2010), Orlando, FL., 5-8 December 2010. [How to Cite?]
 
AbstractINTRODUCTION: Implant surface structure and chemistry determines the contacting cell’s fate. Therefore, the fate of those cells directly affect bone-implant incorporation in clinical practice1-5. However, how these chemical and mechanical signals translating to cellular responses are not yet known. The major drawback is a lack of systematic study of cellbiomaterial interaction in terms of protein expression, specifically, at the attachment interface between the cell and biomaterial (adherence surface, AS). Therefore, we have proposed to unbiasedly identify the biomolecules at the interface by proteomics. This method combines the use of a subcellular fractionation with quantitative mass …
 
DescriptionSession: Controlling Microenvironment and Cell Fate: abstract no. 789
 
DC FieldValue
dc.contributor.authorTong, WY
 
dc.contributor.authorLiang, YM
 
dc.contributor.authorTam, V
 
dc.contributor.authorYip, HK
 
dc.contributor.authorKao, YT
 
dc.contributor.authorCheung, KMC
 
dc.contributor.authorYeung, KWK
 
dc.contributor.authorLam, YW
 
dc.date.accessioned2012-08-16T06:08:35Z
 
dc.date.available2012-08-16T06:08:35Z
 
dc.date.issued2010
 
dc.description.abstractINTRODUCTION: Implant surface structure and chemistry determines the contacting cell’s fate. Therefore, the fate of those cells directly affect bone-implant incorporation in clinical practice1-5. However, how these chemical and mechanical signals translating to cellular responses are not yet known. The major drawback is a lack of systematic study of cellbiomaterial interaction in terms of protein expression, specifically, at the attachment interface between the cell and biomaterial (adherence surface, AS). Therefore, we have proposed to unbiasedly identify the biomolecules at the interface by proteomics. This method combines the use of a subcellular fractionation with quantitative mass …
 
dc.description.naturepostprint
 
dc.descriptionSession: Controlling Microenvironment and Cell Fate: abstract no. 789
 
dc.description.otherThe 2010 North America Conference of the Tissue Engineering and Regenerative Medicine International Society (TERMIS-NA 2010), Orlando, FL., 5-8 December 2010.
 
dc.identifier.citationThe 2010 North America Conference of the Tissue Engineering and Regenerative Medicine International Society (TERMIS-NA 2010), Orlando, FL., 5-8 December 2010. [How to Cite?]
 
dc.identifier.hkuros204564
 
dc.identifier.urihttp://hdl.handle.net/10722/160358
 
dc.languageeng
 
dc.publisherTERMIS-NA.
 
dc.publisher.placeUnited States
 
dc.relation.ispartofTERMIS-Americas 2010 Orlando Conference
 
dc.rightsCreative Commons: Attribution 3.0 Hong Kong License
 
dc.titleProfiling biomolecules at cell-biomaterial interface by quantitative proteomics
 
dc.typeConference_Paper
 
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<contributor.author>Liang, YM</contributor.author>
<contributor.author>Tam, V</contributor.author>
<contributor.author>Yip, HK</contributor.author>
<contributor.author>Kao, YT</contributor.author>
<contributor.author>Cheung, KMC</contributor.author>
<contributor.author>Yeung, KWK</contributor.author>
<contributor.author>Lam, YW</contributor.author>
<date.accessioned>2012-08-16T06:08:35Z</date.accessioned>
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<description>Session: Controlling Microenvironment and Cell Fate: abstract no. 789</description>
<description.abstract>INTRODUCTION: Implant surface structure and chemistry determines the contacting cell&#8217;s fate. Therefore, the fate of those cells directly affect bone-implant incorporation in clinical practice1-5. However, how these chemical and mechanical signals translating to cellular responses are not yet known. The major drawback is a lack of systematic study of cellbiomaterial interaction in terms of protein expression, specifically, at the attachment interface between the cell and biomaterial (adherence surface, AS). Therefore, we have proposed to unbiasedly identify the biomolecules at the interface by proteomics. This method combines the use of a subcellular fractionation with quantitative mass &#8230;</description.abstract>
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