RUI:Test and Measurement Strategies for the Development of Biological Nanovalves
RUI:Test and Measurement Strategies for the Development of Biological Nanovalves
批准号:
2105892
负责人:
Daniel Burden
金额:
$35.21万
依托单位:
依托单位国家:
美国
项目类别:
Continuing Grant
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-06-01 至 2025-05-31
中文摘要
在化学学部化学测量和成像项目的支持下,以及化学、生物工程、环境和运输系统学部界面工程项目的共同资助下,Daniel Burden博士,Lisa Keranen-Burden博士,和他们在惠顿学院化学系的团队正在开发一套新的基于激光的工具,将超灵敏显微镜与电测量和蛋白质工程相结合,以监测带电物质通过纳米孔的运动,其中蛋白质毒素被用作纳米阀。他们的研究寻求一些问题的答案,比如什么样的分子大小、形状和电荷状态可以通过纳米级阀门内部流动,以及需要对纳米阀门进行什么样的化学修饰才能使其根据需要从完全打开状态切换到完全关闭状态。所获得的见解可能会对广泛的应用有用,包括选择性进入细胞内部以对抗感染,纳米级分离和化学传感器。研究团队还通过投资本科研究,努力提高高级STEM学位合格候选人的规模和多样性。研究的要素被整合到本科课程、夏季研究机会和周围社区的公共宣传活动中。离子通道电生理学中的测量方法传统上用于监测带电物质通过纳米孔的运动。然而,许多翻译事件是电静默的,无法检测到。此外,了解可以运输(或阻断)的物质的大小、形状、电荷状态和流速,以及它们与纳米阀门控机制的关系,对于开发该领域的未来应用至关重要。伯顿小组正在研究是否可以对α - hl毒素蛋白进行化学修饰,以可逆地阻止或允许分子流动。他们还假设,在触发阀门关闭时,输送分子的大小和速率会发生显著变化。他们正在开发基于宽视场荧光显微镜、单分子共聚焦显微镜和离子通道电生理学的测量工具,以测试一系列纳米阀结构,最终目标是实时监测基于芯片的双层仪器中脂质膜上的分子运输。pi正在与多名本科生合作,特别是向芝加哥地区第一代即将上大学的非裔美国人或拉丁裔学生伸出援手。pi还积极与外展出版商合作,以改善向公众传播研究成果。该奖项反映了美国国家科学基金会的法定使命,并通过使用基金会的知识价值和更广泛的影响审查标准进行评估,被认为值得支持。
英文摘要
With support from the Chemical Measurement and Imaging Program in the Division of Chemistry and co-funding from the Interfacial Engineering Program in the Division of Chemical, Bioengineering, Environmental, and Transport Systems, Dr. Daniel Burden, Dr. Lisa Keranen-Burden, and their group in the Chemistry Department at Wheaton College are developing a new set of laser-based tools that combine ultrasensitive microscopy with electrical measurements and protein engineering to monitor the movement of charged species through nanopores wherein protein toxins are used as nanovalves. Their studies seek answers to questions such as what molecular sizes, shapes, and charge states are allowed to flow through the nanoscale valve interior, and what chemical modifications to the nanovalve are necessary to make it switchable on demand from the fully-on state to the fully-off state. The insights gained will likely be useful for a broad range of applications, including selective access to the interior of cells to fight infections, nanoscale separations, and chemical sensors. The research team is also working to enhance the size and diversity of the pool of qualified candidates for advanced STEM degrees by investing in undergraduate research. Elements of the research are integrated into the undergraduate curriculum, summer research opportunities, and public outreach activities in the surrounding community. Measurement methods in ion-channel electrophysiology have traditionally been used to monitor the movement of charged species through nanopores. However, many translation events are electrically silent and cannot be detected. Furthermore, an understanding of the sizes, shapes, charge states, and flow rates of species that can be transported (or blocked), as well as their relationship to nanovalve gating mechanisms, is critically important for developing future applications within the field. The Burden group is investigating whether the alpha-HL toxin protein can be chemically modified to reversibly halt or permit molecular flow on demand. They also hypothesize that the size and rate of transported molecules will shift markedly upon triggered valve closure. They are developing measurement tools based on wide-field fluorescence microscopy, single-molecule confocal microscopy, and ion-channel electrophysiology to test a range of nanovalve constructs, with the ultimate aim of monitoring molecular transport across lipid membranes in a chip-based bilayer apparatus in real time. The PIs are working with multiple undergraduate students, reaching out particularly to first-generation college-bound African-American or Latino students from the Chicago area. The PIs are also actively working with outreach publishers to improve communicating research outcomes to the public.This award reflects NSF's statutory mission and has been deemed worthy of support through evaluation using the Foundation's intellectual merit and broader impacts review criteria.
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RUI: Characterizing Protein Nanopores with Modified Caps
-
批准号:1305733
-
项目类别:Standard Grant
-
资助金额:$29.94万
-
财政年份:2013
-
负责人:Daniel Burden
-
依托单位:
RUI:Enhancing Single-Molecule Microscopy for Ion Channel Characterization in Lipid Membranes
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批准号:0957197
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项目类别:Continuing Grant
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资助金额:$25.2万
-
财政年份:2010
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负责人:Daniel Burden
-
依托单位:
MRI-R2: Acquisition of Instruments for Characterizing Soft Interfaces on the Nanoscale and Single-Molecule Levels
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批准号:0958697
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项目类别:Standard Grant
-
资助金额:$40.0万
-
财政年份:2010
-
负责人:Daniel Burden
-
依托单位:
MRI: Instrument Acquisition to Enable Time-Resolved Single-Molecule Fluorescence Measurements at Wheaton College
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批准号:0722688
-
项目类别:Standard Grant
-
资助金额:$38.58万
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财政年份:2007
-
负责人:Daniel Burden
-
依托单位:
RUI:Characterizing interfacial diffusion in biomembranes and polymer thin films with single-molecule fluorescence microscopy
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批准号:0550005
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项目类别:Standard Grant
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资助金额:$27.13万
-
财政年份:2006
-
负责人:Daniel Burden
-
依托单位:
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