Mechanism of Pore Formation BC12 Family Proteins

BC12 家族蛋白的孔隙形成机制

• 批准号: 6844859
• 负责人: PAUL H SCHLESINGER
• 金额: $ 26.78万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-02-01 至 2007-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/6844859
• 关键词: BCL2 gene /protein; apoptosis; chemical kinetics; cytochrome c; lipid bilayer membrane; liposomes; membrane channels; membrane permeability; membrane reconstitution /synthesis; membrane transport proteins; mitochondria; mitochondrial membrane; mutant; pore forming protein; protein localization; protein structure function; stoichiometry; transposon /insertion element; voltage /patch clamp

DESCRIPTION (provided by applicant): Programmed cell death is critical in growth, differentiation and homeostasis of multicellular organisms. The morphologic expression of programmed cell death, apoptosis, has a genetic basis that is clearly dependent on the BCL-2-family proteins. This family of proteins determines an early common decision point in programmed cell death. Structural studies on pro- and anti-apoptotic members of this family indicate they are related to diphtheria and colicin toxins. These proteins insert into membranes, form ion channels and participate in protein translocation. We and others have characterized the channel forming activities of the BCL-2-family members. Studies concerning these proteins have focused on the possibility that they play an important role in increased mitochondrial permeability and in release of cytochrome c. In studies preliminary to this proposal we have demonstrated that BAX forms large water filled pores in artificial liposomes. These pores undergo a concentration dependent dimer to tetramer transition, increasing their size sufficiently to activate cytochrome c transfer across the lipid bilayer. This transition occurs at nanomolar BAX concentrations, in physiologic salt and at physiologic pH without the addition of other proteins, tn this proposal we plan to study and characterize the molecular basis for formation and activation of the large BAX and BID pores, including kinetics, stoichiometry, and the effect of interaction with anti-and pro-apoptotic family members. We will also determine the effect on pore activation of the mitochondrial membrane environment.

描述（申请人提供）：程序性细胞死亡是多细胞生物生长、分化和体内平衡的关键。程序性细胞死亡（凋亡）的形态学表达具有明显依赖于bcl -2家族蛋白的遗传基础。这个蛋白家族决定了程序性细胞死亡的早期共同决策点。对该家族的促凋亡和抗凋亡成员的结构研究表明，它们与白喉和粘菌素毒素有关。这些蛋白质插入细胞膜，形成离子通道并参与蛋白质易位。我们和其他人对bcl -2家族成员的通道形成活动进行了表征。关于这些蛋白质的研究主要集中在它们在增加线粒体通透性和细胞色素c释放中发挥重要作用的可能性上。在本提议的初步研究中，我们已经证明BAX在人工脂质体中形成了充满水的大孔。这些孔经历浓度依赖二聚体到四聚体的转变，增加它们的大小足以激活细胞色素c在脂质双分子层上的转移。这种转变发生在纳摩尔BAX浓度下，在生理盐和生理pH下，没有添加其他蛋白质，在本提案中，我们计划研究和表征大BAX和BID孔形成和激活的分子基础，包括动力学，化学计量学，以及与抗和促凋亡家族成员相互作用的影响。我们还将确定线粒体膜环境对孔隙活化的影响。