Single-molecule analysis of kinesin motors in live cells

活细胞中驱动蛋白马达的单分子分析

• 批准号: 7916802
• 负责人: Kristen J. Verhey
• 金额: $ 28.06万
• 依托单位: UNIVERSITY OF MICHIGAN AT ANN ARBOR
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-28 至 2011-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7916802
• 关键词: Affect; Binding; Biological; Biophysics; Cell division; Cell physiology; Cells; Cellular biology; Characteristics; Chemicals; Color; Complex; Crowding; Cytoplasm; Cytoskeletal Filaments; Defect; Device or Instrument Development; Diagnostic; Diffuse; Dimerization; Disease; Environment; Event; Family member; Fibroblasts; Fluorescence; Fluorescence Microscopy; Fluorescent Dyes; Genetic; Genetic Transcription; Goals; Image; Imaging Techniques; In Vitro; Individual; Intracellular Transport; Investigation; Journals; Kinesin; Label; Length; Life; Link; Malignant Neoplasms; Measures; Mechanics; Membrane Protein Traffic; Methodology; Methods; Microtubule-Associated Proteins; Microtubules; Molecular Motors; Motor; Movement; Mutagenesis; Neurodegenerative Disorders; Neurons; Noise; Organelles; Peptides; Physical Chemical Technique; Polycystic Kidney Diseases; Post-Translational Protein Processing; Property; Proteins; Protocols documentation; Running; Science; Screening procedure; Solvents; Speed; Structure; Synaptic Transmission; System; Techniques; Temperature; Testing; Translations; Vesicle; Virus Diseases; Viscosity; Work; base; biological systems; cell motility; cell type; engineering design; fluorescence imaging; in vivo; insight; motor control; nanoscale; single molecule; tau Proteins; trafficking

DESCRIPTION (provided by applicant): Our long-term goal is to understand the mechanisms by which molecular motors drive directional traffic along cytoskeletal filaments in the crowded cellular milieu. Specifically, we aim to understand how kinesin motors, whose biophysical characteristics have been well-studied in vitro, drive the transport of organelles and vesicles along microtubule tracks in vivo. To do this requires new techniques for nanoscale tracking of the distribution, activity and interactions of individual molecules in the cytoplasm. By combining techniques from the physical, chemical, biological and mathematical sciences, we have developed new methodologies, based on genetic labeling with fluorescent proteins and total internal reflection fluorescence (TIRF) microscopy, that provide the first analysis of single Kinesin-1 motors in the cytoplasm of live cells. Using this system, single molecule imaging in live-cells (SMILe), we have shown that the motility of single truncated Kinesin-1 motors is not hindered by the crowded cellular environment nor upregulated by unknown cellular factors (Biophysical Journal, in press). Understanding how single motors work in vivo is an essential first step to answer cellular questions such as how multiple motors assemble together and integrate their activities to drive membrane trafficking events along crowded microtubules. In Aim 1, we will continue to develop SMILe methodologies for imaging at the nanoscale and use these methods to test other systems (e.g. other kinesins, neuronal cells) and various conditions (e.g. different temperatures and co-expressed accessory proteins). In Aim 2, we will develop two-color SMILe methodologies to characterize the influence of cellular crowding on kinesin motors. In Aim 3, we will use the two-color methodologies to examine the interactions and activities of multiple motors and how they cooperate to drive motility of individual cargoes in live cells. The results of this application will give new insights into the biophysical parameters that control motor protein-based transport. The methods and approaches advanced in this application will be applicable to a wide variety of biological systems (transcription, translation, synaptic transmission, membrane trafficking, etc.) that are driven by the action of a surprisingly low number of molecules. In addition, these results will aid in the design of engineering and diagnostic devices and the development of treatments for neurodegenerative diseases, cancer and viral infection. Project Narrative: The movement of proteins, organelles, and other cellular components is driven by molecular motors. Defects in motor-driven transport have been shown to be associated with neurodegenerative diseases, cancer, and polycystic kidney disease. Understanding how molecular motors function in cells will provide important new targets for therapies aimed at these diseases.

描述（由申请人提供）：我们的长期目标是了解分子马达在拥挤的细胞环境中沿沿着细胞骨架细丝驱动定向交通的机制。具体来说，我们的目标是了解如何驱动蛋白电机，其生物物理特性已在体外研究，驱动器和囊泡的运输沿着微管轨道在体内。要做到这一点，需要新的纳米级技术来跟踪细胞质中单个分子的分布、活动和相互作用。通过结合物理，化学，生物和数学科学的技术，我们开发了新的方法，基于荧光蛋白和全内反射荧光（TIRF）显微镜的遗传标记，提供了活细胞胞质中单个驱动蛋白-1马达的第一次分析。使用该系统，活细胞中的单分子成像（SMILe），我们已经表明，单个截短的驱动蛋白-1马达的运动性不受拥挤的细胞环境的阻碍，也不受未知细胞因子的上调（Biophysical Journal，出版中）。了解单个马达如何在体内工作是回答细胞问题的重要第一步，例如多个马达如何组装在一起并整合它们的活动以驱动膜运输事件沿着拥挤的微管。在目标1中，我们将继续开发用于纳米级成像的SMILe方法，并使用这些方法来测试其他系统（例如其他驱动蛋白，神经元细胞）和各种条件（例如不同温度和共表达的辅助蛋白）。在目标2中，我们将开发双色SMILe方法来表征细胞拥挤对驱动蛋白马达的影响。在目标3中，我们将使用双色方法来研究多个马达的相互作用和活动，以及它们如何合作来驱动活细胞中单个货物的运动。这一应用的结果将提供新的见解的生物物理参数控制马达蛋白为基础的运输。本申请中提出的方法和途径将适用于各种各样的生物系统（转录、翻译、突触传递、膜运输等）。由数量少得令人惊讶的分子的作用驱动。此外，这些结果将有助于工程和诊断设备的设计以及神经退行性疾病，癌症和病毒感染治疗的发展。 项目叙述：蛋白质，细胞器和其他细胞成分的运动是由分子马达驱动的。马达驱动的运输缺陷已被证明与神经退行性疾病、癌症和多囊肾病有关。了解分子马达在细胞中的功能将为针对这些疾病的治疗提供重要的新靶点。