PROTEIN IMPORT INTO NUCLEUS

蛋白质输入细胞核

• 批准号: 7954051
• 负责人: MICHAEL P ROUT
• 金额: $ 0.47万
• 依托单位: ROCKEFELLER UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-03-01 至 2010-02-28
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7954051
• 关键词: Affinity; Cell Nucleus; Cells; Computer Retrieval of Information on Scientific Projects Database; Cytoplasm; Cytoplasmic Protein; Dissociation; Funding; Grant; Institution; Karyopherins; Kinetics; Manuscripts; Measurement; Measures; Methods; Modeling; Nuclear Import; Nuclear Localization Signal; Nuclear Pore Complex; Nuclear Pore Complex Proteins; Process; Publishing; Pump; Research; Research Personnel; Resources; Route; Sampling; Source; Staging; United States National Institutes of Health; Work; Yeasts; in vivo; insight; macromolecule

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. Many cargoes destined for nuclear import carry nuclear localization signals that are recognized by karyopherins (Kaps). We present methods to quantitate import rates and measure Kap and cargo concentrations in single yeast cells in vivo, providing new insights into import kinetics. By systematically manipulating the amounts, types, and affinities of Kaps and cargos, we show that import rates in vivo are simply governed by the concentrations of Kaps and their cargo and the affinity between them. These rates fit to a straightforward pump-leak model for the import process. Unexpectedly, we deduced that the main limiting factor for import is the poor ability of Kaps and cargos to find each other in the cytoplasm in a background of overwhelming nonspecific competition, rather than other more obvious candidates such as the nuclear pore complex and Ran. It is likely that most of every import round is taken up by Kaps and nuclear localization signals sampling other cytoplasmic proteins as they locate each other in the cytoplasm. a manuscript describing the early stages of this work has been published: Simple kinetic relationships and nonspecific competition govern nuclear import rates in vivo. Timney BL, Tetenbaum-Novatt J, Agate DS, Williams R, Zhang W, Chait BT, Rout MP.J Cell Biol. 2006 175(4):579-93. Currently this work is being expanded to include measurements of the dissociation constants between a variety of transport factors and FG-nucleoporins.

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