Lipid nanotube arrays for membrane protein biochips
Lipid nanotube arrays for membrane protein biochips
批准号:
7350191
负责人:
ALEX I. SMIRNOV
金额:
$24.3万
依托单位国家:
美国
项目类别:
财政年份:
2005
资助国家:
美国
项目状态:
已结题
起止时间:
2005-02-01 至 2012-01-31
关键词:
Aluminum OxideAreaBacterial Reaction Center ProteinBenchmarkingBindingBiochemicalBiologicalBiological AssayBiological ModelsBuffersCaliberCartoonsCellsChargeChemistryCholesterolClassComplexConditionDepositionDetectionDevelopmentDiffusionDrug Delivery SystemsElementsEnergy TransferEventFigs - dietaryFilmFluorescenceFluorescence MicroscopyGoalsHeadHumidityHybridsImageIndividualIntakeKnowledgeLateralLengthLifeLife Cycle StagesLipidsLiposomesMapsMeasurementMembraneMembrane ProteinsMethodsModelingMolecularMolecular ConformationMonitorNanotubesOptical MethodsOpticsPatternPeptidesPeripheralPharmaceutical PreparationsPhasePhospholipidsPlayProcessPropertyProtein BindingProtein MicrochipsProteinsProteomePurposeRangeReactionReadingReportingResearchRoleScreening procedureSignal TransductionSilanesSolidStructureStudy modelsSurfaceSurface Plasmon ResonanceSurface PropertiesTechniquesTechnologyTemperatureTimeTubeVesiclebasebiochipcombinatorialcostdesigndrug developmentelectrical propertyfunctional groupinterestnanodevicenanoporenanoscaleprogramsprotein protein interactionresearch studyself assemblysilanesizetwo-photon
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 broad objective of this project is to develop a new class of nanoscale objects - substrate-supported lipid nanotubes - with the goal of building robust hybrid nanodevices that are based on functional membrane proteins. Recently, our lab demonstrated that under certain conditions many phospholipids would self assemble into a nanotube when placed inside a nanopore. For macroscopically homogeneous and uniformly stacked nanopores, these lipid nanotubes form arrays that could be used in combinatorial assays. It was also found, that despite being of a nanoscale size, many properties of these membranes are remarkably similar to those of unsupported bilayers. Thus, it is hypothesized that the lipid nanotubes may serve as suitable mimics of biomembranes in supporting, protecting, and organizing functional membrane proteins. Because biological membranes and associated proteins represent the most attractive drug targets, it is proposed to utilize lipid nanotube design in membrane protein biochips. Preliminary results indicate that the lipid nanotube arrays appear to have several advantages over substrate-supported bilayers of the planar design: much larger bilayer surface area per that of a substrate, protection from surface contaminants, and long shelf time. The following aims are proposed. Aim 1 - Self-assembly of lipid nanotubes: It is proposed to study the mechanism of the lipid nanotube self-assembly in order to gain control of the nanotube properties by manipulating the size of the nanoporous substrate and its surface properties; Aim 2 - Membrane protein biochips: To develop conceptual design of protein biochips based on lipid nanotube arrays that would efficiently detect and analyze molecular interactions of analytes with specific phospholipid membrane and membrane protein targets. Aim 3 - Membrane proteins in lipid nanotubes: To study molecular mechanisms of interaction of transmembrane peptides, membrane and peripheral proteins with the lipid nanotubes for the explicit purpose of using that information in further development of lipid nanotube biochips.
期刊论文(8)
专著(0)
科研奖励(0)
会议论文
登录
查看更多内容
DOI:
10.1016/j.cplett.2010.02.053
发表时间:
2010-04-01
期刊:
CHEMICAL PHYSICS LETTERS
影响因子:
2.8
作者:
[Banerjee, Amrita, Perez-Castillejos, R., Hahn, D., Smirnov, Alex I., Grebel, H.]
通讯作者:
Grebel, H.
Spin-labeled pH-sensitive phospholipids for interfacial pKa determination: synthesis and characterization in aqueous and micellar solutions.
用于界面 pKa 测定的自旋标记 pH 敏感磷脂:水溶液和胶束溶液中的合成和表征。
DOI:
10.1021/jp810993s
发表时间:
2009
期刊:
The journal of physical chemistry. B
影响因子:
--
作者:
[Voinov,MaximA, Kirilyuk,IgorA, Smirnov,AlexI]
通讯作者:
Smirnov,AlexI
Geometry of hydrogen bonds formed by lipid bilayer nitroxide probes: a high-frequency pulsed ENDOR/EPR study.
脂质双层硝基氧探针形成的氢键的几何形状:高频脉冲 ENDOR/EPR 研究。
DOI:
10.1021/ja068395v
发表时间:
2007
期刊:
Journal of the American Chemical Society
影响因子:
15
作者:
[Smirnova,TatyanaI, Smirnov,AlexI, Paschenko,SergueiV, Poluektov,OlegG]
通讯作者:
Poluektov,OlegG
Mapping local protein electrostatics by EPR of pH-sensitive thiol-specific nitroxide.
通过 pH 敏感的硫醇特异性硝基氧的 EPR 绘制局部蛋白质静电图。
DOI:
10.1021/bi800272f
发表时间:
2008
期刊:
Biochemistry
影响因子:
2.9
作者:
[Voinov,MaximA, Ruuge,Andres, Reznikov,VladimirA, Grigor'ev,IgorA, Smirnov,AlexI]
通讯作者:
Smirnov,AlexI
DOI:
10.1039/b818184e
发表时间:
2009-05
期刊:
The Analyst
影响因子:
--
作者:
[Woldman YY, Semenov SV, Bobko AA, Kirilyuk IA, Polienko JF, Voinov MA, Bagryanskaya EG, Khramtsov VV]
通讯作者:
Khramtsov VV
共 6 条
Upgrade of Bruker Time-domain EPR Spectrometer
-
批准号:10431412
-
项目类别:
-
资助金额:$59.99万
-
财政年份:2022
-
负责人:ALEX I. SMIRNOV
-
依托单位:
Nanodiamond Quantum Sensors for Free Radical Detection
-
批准号:10325762
-
项目类别:
-
资助金额:$25.66万
-
财政年份:2021
-
负责人:ALEX I. SMIRNOV
-
依托单位:
Time-domain/ELDOR EPR Spectrometer
-
批准号:7596125
-
项目类别:
-
资助金额:$50.0万
-
财政年份:2009
-
负责人:ALEX I. SMIRNOV
-
依托单位:
Lipid nanotube arrays for membrane protein biochips
-
批准号:7010680
-
项目类别:
-
资助金额:$25.03万
-
财政年份:2005
-
负责人:ALEX I. SMIRNOV
-
依托单位:
PROTEIN DEPOSITION ONTO LIPID NANOTUBE ARRAYS
-
批准号:7181258
-
项目类别:
-
资助金额:$0.19万
-
财政年份:2005
-
负责人:ALEX I. SMIRNOV
-
依托单位:
Lipid nanotube arrays for membrane protein biochips
-
批准号:6861523
-
项目类别:
-
资助金额:$26.65万
-
财政年份:2005
-
负责人:ALEX I. SMIRNOV
-
依托单位:
Lipid nanotube arrays for membrane protein biochips
-
批准号:7174700
-
项目类别:
-
资助金额:$24.3万
-
财政年份:2005
-
负责人:ALEX I. SMIRNOV
-
依托单位:
PROTEIN DEPOSITION ONTO LIPID NANOTUBE ARRAYS
-
批准号:6977636
-
项目类别:
-
资助金额:$1.26万
-
财政年份:2004
-
负责人:ALEX I. SMIRNOV
-
依托单位:
HIGH FREQUENCY EPR OF VIABLE BIOLOGICAL SYSTEMS
-
批准号:6120643
-
项目类别:
-
资助金额:$2.16万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
SECOND W BAND EPR USER STATION
-
批准号:6120623
-
项目类别:
-
资助金额:$2.7万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
HIGH FIELD EPR OF SPIN LABELED HUMAN GROWTH HORMONE
-
批准号:6120625
-
项目类别:
-
资助金额:$1.62万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
EPR LINEWIDTH (T2) METHOD TO MEASURE MEMBRANE OXYGEN PERMEABILITY
-
批准号:6120615
-
项目类别:
-
资助金额:$0.16万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
COMPARATIVE SPIN LABEL SPECTRA AT X BAND (9 5 GHZ) & W BAND (95 GHZ)
-
批准号:6120618
-
项目类别:
-
资助金额:$0.32万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
RADICAL SPECIES IN BREWED COFFEE & TEA BIOLOGICAL ANTIOXIDANTS
-
批准号:6120657
-
项目类别:
-
资助金额:$0.11万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
EFFECT OF LOW ETHANOL CONCENTRATIONS ON MEMBRANES
-
批准号:6120616
-
项目类别:
-
资助金额:$0.27万
-
财政年份:1998
-
负责人:ALEX I. SMIRNOV
-
依托单位:
COMPARATIVE SPIN LABEL SPECTRA AT X BAND (9 5 GHZ) & W BAND (95 GHZ)
-
批准号:6251815
-
项目类别:
-
资助金额:$0.42万
-
财政年份:1997
-
负责人:ALEX I. SMIRNOV
-
依托单位:
RADICAL SPECIES IN BREWED COFFEE & TEA: BIOLOGICAL ANTIOXIDANTS
-
批准号:6251778
-
项目类别:
-
资助金额:$0.42万
-
财政年份:1997
-
负责人:ALEX I. SMIRNOV
-
依托单位:
SECOND W BAND EPR USER STATION
-
批准号:6251828
-
项目类别:
-
资助金额:$0.42万
-
财政年份:1997
-
负责人:ALEX I. SMIRNOV
-
依托单位:
RAPID QUANTITATION OF INHOMOGENEOUS EPR SPECTRA BY FAST CONVOLUTION
-
批准号:6251771
-
项目类别:
-
资助金额:$0.42万
-
财政年份:1997
-
负责人:ALEX I. SMIRNOV
-
依托单位:
EPR IMAGING OF NATURAL FREE RADICALS IN ROASTED COFFEE BEANS
-
批准号:6251767
-
项目类别:
-
资助金额:$0.42万
-
财政年份:1997
-
负责人:ALEX I. SMIRNOV
-
依托单位:
国内基金
海外基金
层出镰刀菌氮代谢调控因子AreA 介导伏马菌素 FB1 生物合成的作用机理
-
批准号:2021JJ40433
-
项目类别:省市级项目
-
资助金额:--
-
批准年份:2021
-
负责人:孙磊
-
依托单位:
寄主诱导梢腐病菌AreA和CYP51基因沉默增强甘蔗抗病性机制解析
-
批准号:32001603
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:段真珍
-
依托单位:
AREA国际经济模型的移植.改进和应用
-
批准号:18870435
-
项目类别:面上项目
-
资助金额:2.0万元
-
批准年份:1988
-
负责人:史树中
-
依托单位: