Expressed Bacterial Triple-Helical Products as Tissue Engineering Scaffolds
Expressed Bacterial Triple-Helical Products as Tissue Engineering Scaffolds
批准号:
7296100
负责人:
BARBARA M BRODSKY
金额:
$26.42万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-29 至 2009-08-31
关键词:
AddressAnimalsAttentionBasement membraneBasic ScienceBindingBinding SitesBiocompatible MaterialsBiologicalCell AdhesionCellsCharacteristicsChimera organismCollagenCollagen Type ICollagen Type IVDisruptionEscherichia coliHeparin BindingHigher Order Chromatin StructureHumanHydration statusHydroxyprolineIntegrin BindingIntegrinsInterruptionLeadLengthLigandsLocationMatrix MetalloproteinasesModelingMolecularMorphologyN-terminalNaturePliabilityPolymersPost-Translational Protein ProcessingProductionPropertyProteinsRangeRecombinant ProteinsRecombinantsResearchResearch PersonnelScientistShockSiteSolubilityStem cellsStreptococcus pyogenesStructureSystemTissue Engineeringbasedesigndesireimprovednovelnovel strategiespolypeptideprogramsscaffoldtriple helixvector
中文摘要
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (provided by applicant): The unique properties of the collagen triple-helix motif include its molecular hydrodynamic properties, extensive hydration, ability to bind diverse ligands, and the capacity self-associate to form fibrils and other higher order structures. These distinctive features have been exploited by nature to fill a wide range of structural and functional niches, and by scientists to design numerous products important for biomaterial and biomedical uses. Because of problems and concerns with the use of extracted collagens, attention has shifted to production of recombinant animal collagens, but efficient production has been slowed down addressing issues of post-translational modification. Rather than focus on specific types of animal collagens, we propose to focus on the intrinsic properties of the motif, using a bacterial triple-helix module which has high stability with no post-translational modifications. Stable triple-helix modules based on bacterial "collagen-like" sequences will be utilized to form triple-helical polymers in a high yield E. coli cold shock expression system. Repeating modules will be used to attain lengths comparable to that of animal fibril forming collagens, and we hypothesize that these triple-helical proteins will self-assemble to form fibrillar structures. Defined human collagen sequences involved in known interactions will be inserted between adjacent bacterial collagen modules to produce chimeras with functional binding sites. Introduction of basement membrane type breaks in the repeating (Gly-X-Y)n sequence between bacterial triple-helix modules will used to create a flexible or kinked type structure that more closely models basement membrane collagen networks and may provide a substrate for stem cell cultures. This novel approach plans to capture the flexibility and advantages of the collagen triple-helix motif while retaining the simplicity of a bacterial expression system. The products of this system will be ideal for manipulations and applications as scaffolds in tissue engineering. Lay Summary: A novel approach to gain efficient production of repeating bacterial collagen-like sequences plans to capture the flexibility and advantages of the collagen triple-helix motrf while retaining the simplicity of a bacterial expression system. The products of this system will be ideal for manipulations and applications as scaffolds in tissue engineering.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Noncollagenous region of the streptococcal collagen-like protein is a trimerization domain that supports refolding of adjacent homologous and heterologous collagenous domains.
链球菌胶原蛋白样蛋白的非胶原区域是一个三聚化结构域,支持相邻同源和异源胶原结构域的重折叠。
DOI:
10.1002/pro.356
发表时间:
2010
期刊:
Protein science : a publication of the Protein Society
影响因子:
--
作者:
[Yu,Zhuoxin, Mirochnitchenko,Oleg, Xu,Chunying, Yoshizumi,Ayumi, Brodsky,Barbara, Inouye,Masayori]
通讯作者:
Inouye,Masayori
Dissecting a bacterial collagen domain from Streptococcus pyogenes: sequence and length-dependent variations in triple helix stability and folding.
剖析化脓性链球菌的细菌胶原结构域:三螺旋稳定性和折叠的序列和长度依赖性变化。
DOI:
10.1074/jbc.m110.217422
发表时间:
2011
期刊:
The Journal of biological chemistry
影响因子:
--
作者:
[Yu,Zhuoxin, Brodsky,Barbara, Inouye,Masayori]
通讯作者:
Inouye,Masayori
Biomaterial Applications of Recombinant Bacterial Collagens
-
批准号:8323975
-
项目类别:
-
资助金额:$32.42万
-
财政年份:2010
-
负责人:BARBARA M BRODSKY
-
依托单位:
Biomaterial Applications of Recombinant Bacterial Collagens
-
批准号:8040223
-
项目类别:
-
资助金额:$34.34万
-
财政年份:2010
-
负责人:BARBARA M BRODSKY
-
依托单位:
Biomaterial Applications of Recombinant Bacterial Collagens
-
批准号:8523854
-
项目类别:
-
资助金额:$30.03万
-
财政年份:2010
-
负责人:BARBARA M BRODSKY
-
依托单位:
Biomaterial Applications of Recombinant Bacterial Collagens
-
批准号:8152151
-
项目类别:
-
资助金额:$33.0万
-
财政年份:2010
-
负责人:BARBARA M BRODSKY
-
依托单位:
Stuctural studies of triple-helical proteins
-
批准号:7923559
-
项目类别:
-
资助金额:$15.34万
-
财政年份:2009
-
负责人:BARBARA M BRODSKY
-
依托单位:
Stuctural studies of triple-helical proteins
-
批准号:8127215
-
项目类别:
-
资助金额:$19.82万
-
财政年份:2009
-
负责人:BARBARA M BRODSKY
-
依托单位:
Expressed Bacterial Triple-Helical Products as Tissue Engineering Scaffolds
-
批准号:7177983
-
项目类别:
-
资助金额:$15.55万
-
财政年份:2006
-
负责人:BARBARA M BRODSKY
-
依托单位:
Analysis of collagen and coiled coil mutations
-
批准号:6843060
-
项目类别:
-
资助金额:$0.55万
-
财政年份:2004
-
负责人:BARBARA M BRODSKY
-
依托单位:
Analysis of collagen and coiled coil mutations
-
批准号:6739861
-
项目类别:
-
资助金额:$5.15万
-
财政年份:2004
-
负责人:BARBARA M BRODSKY
-
依托单位:
Acquisition of a Circular Dichroism Spectrometer
-
批准号:6439978
-
项目类别:
-
资助金额:$16.17万
-
财政年份:2002
-
负责人:BARBARA M BRODSKY
-
依托单位:
MICROCALORIMETRY FACILITY
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批准号:6292237
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项目类别:
-
资助金额:$14.76万
-
财政年份:2001
-
负责人:BARBARA M BRODSKY
-
依托单位:
ANALYTICAL ULTRACENTRIFUGE FACILITY
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批准号:2802619
-
项目类别:
-
资助金额:$25.26万
-
财政年份:1999
-
负责人:BARBARA M BRODSKY
-
依托单位:
BIOMEDICAL RESEARCH SUPPORT GRANT
-
批准号:3520867
-
项目类别:
-
资助金额:$12.3万
-
财政年份:1990
-
负责人:BARBARA M BRODSKY
-
依托单位:
STRUCTURAL STUDIES OF CONNECTIVE TISSUE
-
批准号:2078438
-
项目类别:
-
资助金额:$17.84万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
Structural Studies of Triple-Helical Proteins
-
批准号:6788065
-
项目类别:
-
资助金额:$30.77万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
Structural Studies of Triple-Helical Proteins
-
批准号:6610524
-
项目类别:
-
资助金额:$32.99万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
Stuctural studies of triple-helical proteins
-
批准号:7680054
-
项目类别:
-
资助金额:$32.6万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
Stuctural studies of triple-helical proteins
-
批准号:7934672
-
项目类别:
-
资助金额:$31.76万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
STRUCTURAL STUDIES OF CONNECTIVE TISSUE
-
批准号:2517423
-
项目类别:
-
资助金额:$18.55万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
STRUCTURAL STUDIES OF TRIPLE HELICAL PROTEINS
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批准号:6012440
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项目类别:
-
资助金额:$28.45万
-
财政年份:1977
-
负责人:BARBARA M BRODSKY
-
依托单位:
海外基金