COLLABORATIVE RESEARCH: HIGH-SPEED AFM IMAGING OF DYNAMICS ON BIOPOLYMERS THROUGH NON-RASTER SCANNING
COLLABORATIVE RESEARCH: HIGH-SPEED AFM IMAGING OF DYNAMICS ON BIOPOLYMERS THROUGH NON-RASTER SCANNING
批准号:
1461593
负责人:
Kam Leang
金额:
$23.67万
依托单位:
依托单位国家:
美国
项目类别:
Standard Grant
财政年份:
2014
资助国家:
美国
项目状态:
已结题
起止时间:
2014-08-15 至 2018-07-31
中文摘要
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英文摘要
This award by the Instrument Development for Biological Research (IDBR) program in the Division of Biological Infrastructure (BIO Directorate) is co-funded by the Particulate and Multiphase Processes (PMP) program in the Division of Chemical, Bioengineering, Environmental, and Transport Systems (CBET, Engineering Directorate).Non Technical AbstractThe primary aim of this project is to create a novel high-speed atomic force microscope (AFM) imaging system with frame rates of on the order of 100 frames/second. While the creation of this instrument may have a significant impact on a broad range of application areas, the primary target is the study of biomolecular processes. The extremely fast frame rate and long range will allow for the direct visualization of dynamic process that previously could be studied at best only through indirect means. The interdisciplinary nature of the project provides excellent opportunities for both graduate and undergraduate student training as well as outreach to middle- and high-school age students through summer programs on nano- and biotechnology.Technical AbstractThe speed gains of the instrument will be achieved in two ways. The first way is to replace the standard raster-scan of AFM with a feedback algorithm that steers the tip to stay in the region of interest. This will reduce imaging time by reducing the amount of scanning to be done, with the tradeoff that the sample to be imaged must have an underlying string-like structure such as is found in biopolymers. The second way is to create dual-stage scanning systems that will allow the non-raster scanning to be performed at ultra-fast speeds. A prototype system will be built and demonstrated on a variety of standard samples before being deployed to study the dynamics of the molecular motor myosin V. The instrument and underlying techniques will be disseminated through journal publication and conference publication and through collaboration with an existing AFM company to integrate the techniques in their next generation devices.
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