Assembly, dynamics and evolution of cell-cell and cell-matrix adhesions

描述(申请人提供)：细胞黏附复合体是一类具有重要生物医学意义的多蛋白质组装体。它们参与感知细胞与其外部环境之间的相互作用，然后启动和调节细胞内信号，控制细胞迁移、细胞形状和功能组织、增殖和生存以及基因表达。它们在进化上是老的，对正常发育和动态平衡至关重要，而且在遗传病和癌症方面存在缺陷。 目前，缺乏一个协调的努力来整合现有的基因组(进化)和结构信息来严格解决这些多蛋白质复合体在原子、介观和宏观尺度上的分层结构组织。进展的另一个障碍是大量纯化的蛋白质可用于多蛋白质复合体的重组，因为由于复杂蛋白质组装的不稳定性质，经典方法是不可行的。 该联盟将利用大量目标蛋白质家族和信号网络的高通量表达和结构来了解细胞-细胞和细胞-细胞外基质黏附复合体的结构和功能组织。该联盟将整合结构生物学(X射线结晶学、原位复合体的电子显微镜)、生物化学和细胞生物学(体外)方面的专业知识 重组)、化学和活细胞成像(原位生物传感器和笼养蛋白质)： 具体目标1：定义多蛋白质相互作用、化学计量和溶液中的亲和力(Liddington，Weis)。具体目标2：在生物膜上重建多蛋白质复合体(Ginsberg，Nelson)。具体目标3：在生理环境中原位确定多蛋白质复合体的结构(Hanein，Volkmann)。具体目标4：分析活细胞中动态的蛋白质相互作用和组装(HAHN)。

DESCRIPTION (provided by applicant): Cell adhesion complexes are a bio-medically important class of multi-protein assemblies. They are involved in sensing Interactions between cells and their external environment, and then initiating and regulating intracellular signals that control cell migration, cell shape and functional organization, proliferation and survival, and gene expression. They are evolutionarily old, critical for normal development and homeostasis, and are defective in genetic diseases and cancer. Currently, there is a lack of a concerted effort to integrate available genomic (evolutionary) and structural information to rigorously solve the hierarchical structural organization of these multi-protein complexes at the atomic, meso and macro scale. A further barrier to progress is the availability of large amounts of purified proteins for multi-protein complex reconstitution since classical approaches are not feasible due to the unstable nature of complex protein assemblies. The Consortium will leverage high-throughput expression and structures of large sets of target families of proteins and signaling networks to understand the structural and functional organization of both cell-cell and cell-ECM adhesion complexes. The Consortium will integrate expertise in structural biology (X-ray crystallography, electron microscopy of in situ complexes), biochemistry and cell biology (in vitro reconstitution), chemistry and live cell imaging (in situ bio-sensors and caged proteins) by: Specific Aim 1: Define multi-protein interactions, stoichiometries and affinities in solution (Liddington, Weis). Specific Aim 2: Reconstitute multi-protein complexes on biological membranes (Ginsberg, Nelson). Specific Aim 3: Define structures of multi-protein complexes in situ, at a physiological environment (Hanein, Volkmann). Specific Aim 4: Analyze dynamic protein-protein interactions and assembly in live cells (Hahn).