Mechanism of myosin motor-dependent filopodia formation

肌球蛋白运动依赖性丝状伪足形成机制

• 批准号: 10402162
• 负责人: MARGARET A TITUS
• 金额: $ 19.41万
• 依托单位: UNIVERSITY OF MINNESOTA
• 依托单位国家: 美国
• 财政年份: 2017
• 资助国家: 美国
• 起止时间: 2017-09-15 至 2021-08-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10402162
• 关键词: 3-Dimensional; Actins; Administrative Supplement; Biological Models; Cells; Computer Models; Dictyostelium; Environment; Equipment; Filopodia; Goals; In Vitro; Invaded; Knowledge; Length; Membrane; Microfilaments; Modeling; Molecular; Motor; Myosin ATPase; Neurons; Nonmuscle Myosin Type IIA; Process; Property; Proteins; Role; Structure; Tail; Tissues; Work; base; cancer cell; cancer invasiveness; cell type; crosslink; ezrin; in silico; in vivo; migration; moesin; parent project; polymerization; radixin protein; therapeutic development; tumor; vasodilator-stimulated phosphoprotein

Administrative Supplement for Equipment - GM122917 Margaret A. Titus, PI Abstract of Parent Project Cells migrating in tissues, including cancer cells, use filopodia to guide them through the 3D environment and increased formation of filopodia correlates strongly with the metastatic potential and invasiveness of cancer cells. Filopodia are slender actin-filled projections composed of a core of cross-linked, parallel actin bundles. They are highly dynamic, vary in length and are found in a wide variety of cell types such as neurons that use them for gradient sensing and efficient directional migration and cancer cells that employ them for moving out from tumors into neighboring tissue. The first steps of filopodia formation are not well understood. Three conserved proteins are required for their formation - a MyTH4-FERM myosin (MF; MyTH4 = myosin tail homology 4; FERM = band 4.1, ezrin, radixin, moesin) and two regulators of actin polymerization, VASP and Formin. How the action of these three proteins is coordinated to initiate filopodia formation is unknown. The objective of the parent project is to define the molecular mechanism of filopodia initiation with an emphasis on the role of a MF myosin in this process. The versatile model system, Dictyostelium will be used to define how a MF myosin and VASP work together to organize the fast growing ends of actin filaments at the membrane to initiate polymerization. A combination of in vivo, in vitro and in silico approaches will be employed to a) determine the functional relationship between a MF myosin, VASP and formin, b) identify the specific properties of the myosin motor used for filopodia initiation, c) identify proteins that interact with the MF myosin to promote cortical targeting during filopod initiation and filopod tip formation and d) develop a stochastic computational model with predictive power that will inform the experimental goals, the results of which will be used to refine the model. The knowledge generated by the parent project will reveal how cells use a myosin-based motor to build specific actin-based structures such as filopodia. Understanding how initiation occurs will also reveal how cells control filopodia formation to enable directed migration or invasion of surrounding tissues.

设备管理补充- GM122917