CHARACTERIZATION OF KINESIN-3 AND KINESIN-3 CARGO IN TRANSIT WITH THE AXON

使用 Axon 表征 KINESIN-3 和运输中的 KINESIN-3 货物

• 批准号: 7960159
• 负责人: Joseph Alan Degiorgis
• 金额: $ 7.74万
• 依托单位: UNIVERSITY OF RHODE ISLAND
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-05-04 至 2010-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7960159
• 关键词: Anatomy; Antibodies; Axon; Axonal Transport; Behavioral Research; Binding; Computer Retrieval of Information on Scientific Projects Database; Dynein ATPase; Funding; Grant; Institution; Kinesin; Mediating; Membrane; Microtubules; Molecular; Motor; Movement; Organelles; Plus End of the Microtubule; Process; Property; Proteins; Research; Research Personnel; Resources; Role; Source; United States National Institutes of Health; axoplasm; particle

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Axonal transport is a process in which membrane bound particles are in transit along microtubules powered by motor proteins belonging to the kinesin and cytoplasmic dynein superfamilies. Recently we identified a Kinesin-3 (KIF1A) that co-purifies with axoplasmic organelles and localizes to organelle/microtubule interfaces. Antibodies raised against Kinesin-3 decorate 100 nm organelles in extruded axoplasm and inhibit organelle transport towards the plus ends of microtubules. These finding suggest that Kinesin-3 may be responsible for moving 100 nm organelles towards the plus ends of microtubules. Here, we propose to characterize the motor properties of purified Kinesin-3 and to identify the molecular anatomy of the Kinesin-3 cargo. Understanding the rate and direction of Kinesin-3 movement and the molecular composition of its cargo will help establish Kinesin-3's role in the axon and determine its contribution to motor mediated transport.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 轴突运输是一个过程，其中膜结合的颗粒是在运输沿着微管动力属于驱动蛋白和细胞质动力蛋白超家族的马达蛋白。最近，我们发现了一个驱动蛋白-3（KIF 1A），它与轴浆细胞器共纯化，并定位于细胞器/微管界面。针对驱动蛋白-3产生的抗体在挤出的轴浆中装饰100 nm的细胞器并抑制细胞器向微管的正端运输。这些发现表明，驱动蛋白-3可能是负责移动100纳米的细胞器向正端的微管。在这里，我们提出了纯化的驱动蛋白-3的电机特性的特点，并确定驱动蛋白-3货物的分子解剖。了解驱动蛋白-3运动的速率和方向及其货物的分子组成将有助于确定驱动蛋白-3在轴突中的作用，并确定其对运动介导的运输的贡献。