C-SRC BINDING A PHOSPHOPEPTIDE

C-SRC 结合磷酸肽

• 批准号: 7954632
• 负责人: PAUL L SORGEN
• 金额: $ 0.6万
• 依托单位: UNIVERSITY OF WISCONSIN-MADISON
• 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/7954632
• 关键词: Affect; Area; Binding; Biological Models; Brain; Cells; Charcot-Marie-Tooth Disease; Communication; Computer Retrieval of Information on Scientific Projects Database; Connexin 43; Connexins; Coupling; Cytoplasmic Tail; Defect; Disease; Event; Funding; Gap Junctions; Genes; Goals; Grant; Heart; Homeostasis; Human; Inborn Genetic Diseases; Individual; Inherited; Injury; Institution; Ischemia; Metabolic; Molecular; Mus; Organ; Pathway interactions; Phosphopeptides; Phosphorylation; Protein Isoforms; Proteins; Regulation; Research; Research Personnel; Resources; Signal Transduction; Site; Source; System; Testing; Therapeutic; Tissue Preservation; Tissues; United States National Institutes of Health; Work; deafness; design; genetic manipulation; intermolecular interaction; particle; receptor; response

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. The long term goal of our work is to gain a structural and functional understanding of the mechanisms of gap junction regulation. Gap junctions, formed of proteins called connexins (Cxs), provide an intercellular pathway for the propagation of electrical/molecular signals, which are necessary for cellular differentiation, metabolic homeostasis, and in excitable tissue, electrical coupling. This type of communication permits individual cell events to synchronize into the functional response of an entire organ. Defects in human Cx genes that affect cell coupling are associated with a variety of inherited disorders (e.g. Charcot-Marie-Tooth disease and hereditary non-syndromic deafness). Genetic manipulations in mice have demonstrated the functional importance of Cxs in a variety of organs. Moreover, not only the presence but also the proper regulation of gap junctions is critical for homeostasis. For example, intracellular acidification leads to closure of gap junctions in all native tissues and exogenous expression systems tested. The study of pH-dependent regulation of gap junctions becomes even more relevant given that intracellular acidification is a major consequence of tissue ischemia. Acidification-induced uncoupling has an impact on the preservation of tissue surrounding the ischemic area. Therefore, we have chosen Cx43, the most widely expressed junction protein in the heart, brain, and other tissues, as our model system to study the structural regulation of Cxs. Our objective is to apply biophysical approaches to investigate intra- and intermolecular interactions that define the structural regulation of Cx43 during pH gating. We hypothesize that the Cx43 carboxyl terminal domain (CT) acts as a gating "particle" that, under the appropriate conditions (e.g. intracellular acidification or phosphorylation), binds to a "receptor" (i.e. Cx43 cytoplasmic loop; CL) affiliated with the pore and closes the channel. The following Specific Aims are proposed to investigate this concept: 1) To establish how the CT interacts with molecular partners that are involved in gap junction regulation; 2) To assess the structural effect of pH on the CT and CL domains; 3) To characterize cytoplasmic domain interactions between Cx isoforms. These Aims are designed to identify the functional consequences resulting from CT interactions with molecular partners and the CL in an effort to develop site-directed, specific modulators of gap junction communication with potential implications in therapeutic treatment of disease and ischemic injury.

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。 我们工作的长期目标是获得对间隙连接调节机制的结构和功能理解。由称为连接蛋白（Cxs）的蛋白质形成的间隙连接为电/分子信号的传播提供了细胞间途径，这些信号对于细胞分化、代谢稳态和可兴奋组织中的电耦合是必需的。这种类型的通信允许单个细胞事件同步到整个器官的功能反应中。影响细胞偶联的人类Cx基因缺陷与多种遗传性疾病（例如Charcot-Marie-Tooth病和遗传性非综合征性耳聋）相关。小鼠的遗传操作已经证明了Cxs在各种器官中的功能重要性。此外，不仅间隙连接的存在，而且适当的调节是至关重要的稳态。例如，细胞内酸化导致测试的所有天然组织和外源表达系统中间隙连接的闭合。考虑到细胞内酸化是组织缺血的主要后果，缝隙连接的pH依赖性调节的研究变得更加相关。酸化诱导的解偶联对缺血区域周围组织的保存有影响。因此，我们选择了Cx43，在心脏，大脑和其他组织中最广泛表达的连接蛋白，作为我们的模型系统来研究Cxs的结构调控。我们的目标是应用生物物理学方法来研究内和分子间的相互作用，定义Cx43在pH门控的结构调节。我们假设Cx43羧基末端结构域（CT）作为门控“颗粒”，在适当的条件下（例如细胞内酸化或磷酸化），结合到“受体”（即Cx43细胞质环; CL）附属孔和关闭通道。提出了以下具体目的来研究这一概念：1）确定CT如何与参与间隙连接调节的分子伴侣相互作用; 2）评估pH对CT和CL结构域的结构影响; 3）表征Cx亚型之间的胞质结构域相互作用。这些目的旨在确定CT与分子伴侣和CL相互作用产生的功能后果，以开发在疾病和缺血性损伤治疗中具有潜在意义的间隙连接通讯的定点特异性调节剂。