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Lipid nanotube arrays for membrane protein biochips

Lipid nanotube arrays for membrane protein biochips
用于膜蛋白生物芯片的脂质纳米管阵列
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

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中文摘要
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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)
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科研奖励(0)
会议论文
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
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