权益分类	功能权益	普通用户	{{item.name}}会员
{{category.name}}	{{benefitItem.name}}

Structural and Biophysical Characterization of Hedgehog Signaling

Hedgehog 信号传导的结构和生物物理表征

基本信息

批准号：
8606223
负责人：
DANIEL J LEAHY
金额：
$ 33.87万
依托单位：
JOHNS HOPKINS UNIVERSITY
依托单位国家：
美国
项目类别：
财政年份：
2007
资助国家：
美国
起止时间：
2007-05-01 至 2016-01-31
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/8606223
关键词：
Adhesions Affinity Animals Binding Biochemical Biological Assay Breast Calcium Cell Differentiation process Cell Proliferation Cell Surface Proteins Cell surface Cells Clinical Trials Co-Immunoprecipitations Colon Complex Conflict (Psychology)Congenital Abnormality Core Protein Defect Development Differentiation and Growth Drosophila genus Erinaceidae Event Fibronectins Genetic Glycosylphosphatidylinositols Glypican Goals Growth Factor Receptors Heparan Sulfate Proteoglycan Heparin Homologous Gene Homologous Protein Human Immunoglobulins In Vitro Integral Membrane Protein Invertebrates Label Laboratories Lead Lung Malignant Neoplasms Malignant neoplasm of brain Maps Measures Mediating Molecular Nature Organism Pancreas Pathway interactions Pattern Polysaccharides Positioning Attribute Process Protein Binding Proteins Reporting Roentgen Rays Role Signaling Molecule Site Site-Directed Mutagenesis Skin Structure Surface Therapeutic Tissues Vertebrates Work X-Ray Crystallography base biophysical properties cancer therapy cell type fly glypican 3 inhibitor/antagonist insight meetings milligram morphogens patched protein public health relevance receptor reconstitution research study smoothened signaling pathway therapeutic target transmission process vertebrate hedgehog protein

项目摘要

DESCRIPTION (provided by applicant): Hedgehog proteins are secreted signaling molecules that regulate the growth and differentiation of cells during animal development. Hedgehogs meet the classical definition of a morphogen by forming gradients of decreasing concentration that emanate from sites of secretion and induce differentiation of distinct cell types at different positions along the gradient. In this manner Hedgehog proteins mediate the formation of complex tissue patterns. Abnormal Hedgehog signaling can result in severe developmental defects and cancer, and clinical trials assessing the efficacy of Hedgehog signaling inhibitors are underway in cancers of the brain, breast, lung, colon, pancreas, and skin. Perhaps owing to its importance for patterning multiple tissues, the activity of the Hedgehog signaling pathway is tightly regulated. Hedgehog proteins appear to interact with multiple protein and glycan partners that modulate its activity, distribution, or both. The 12-pass integral membrane protein Patched is required for normal reception of Hedgehog signals and has been widely identified as the "Hedgehog receptor", but evidence for direct binding of Hedgehog to Patched is absent in flies and indirect in vertebrates. Several additional cell-surface proteins have been shown to bind directly to Hedgehog proteins with high affinity including Ihog in flies and Cdo, Boc, and Hedgehog-interacting protein in vertebrates. Others, including the protein cores of glypicans and a vertebrate-specific protein Gas1, associate with Hedgehog proteins with weaker affinity or as part of larger complexes and have been suggested as co- receptors for Hedgehog proteins. We have expressed and purified active fragments of Hedgehog, Ihog, Cdo, Boc, glypican, and Gas1 proteins, determined crystal structures of Hh:Ihog, Hh:Cdo, and Hh:Boc complexes, and demonstrated that these interactions depend on additional co-factors including heparin and Ca2+. We have also recently expressed and purified small amounts (~40 ug) of Patched. To investigate the molecular mechanisms governing Hedgehog signaling and understand the nature of the Hedgehog receptor at the molecular level we propose X-ray crystallographic, biophysical, and biochemical studies of these Hh pathway components and their complexes. These studies will elucidate the molecular mechanisms governing activity of the Hedgehog signaling pathway and thus the molecular strategies employed to generate complex tissue pattern. Such studies are also likely to uncover molecular interactions or processes that may be targeted for therapeutic inhibition of Hedgehog signaling. We will achieve these goals by pursuing the following specific aims: (1) determine the molecular mechanisms by which glypicans modulate vertebrate and invertebrate Hedgehog signaling, (2) determine the molecular mechanisms by which Gas1 modulates vertebrate Hedgehog signaling and the interplay between Gas1 and other modulators of Hedgehog signaling, and (3) determine the nature of vertebrate and invertebrate Hedgehog receptor complexes by reconstituting the minimal Hedgehog binding complex in vitro with purified components.

描述（由申请人提供）：刺猬蛋白是在动物发育期间调节细胞生长和分化的分泌信号分子。刺猬通过形成从分泌部位发出的浓度递减的梯度并在沿梯度的沿着不同位置诱导不同细胞类型的分化来满足形态发生素的经典定义。以这种方式，刺猬蛋白介导复杂组织模式的形成。Hedgehog信号异常可导致严重的发育缺陷和癌症，评估Hedgehog信号抑制剂在脑癌、乳腺癌、肺癌、结肠癌、胰腺癌和皮肤癌中疗效的临床试验正在进行中。也许是由于其对多种组织的重要性，刺猬信号通路的活性受到严格调控。刺猬蛋白似乎与多种蛋白质和聚糖伴侣相互作用，调节其活性，分布或两者兼而有之。12通道整合膜蛋白Patched是正常接收Hedgehog信号所必需的，并已被广泛鉴定为“Hedgehog受体”，但Hedgehog与Patched直接结合的证据在果蝇中不存在，在脊椎动物中间接结合。已经显示了几种另外的细胞表面蛋白质以高亲和力直接结合刺猬蛋白，包括蝇中的Ihog和脊椎动物中的Cdo、Boc和刺猬相互作用蛋白。其他的，包括磷脂酰肌醇蛋白聚糖的蛋白质核心和脊椎动物特异性蛋白Gas 1，以较弱的亲和力与刺猬蛋白结合或作为较大复合物的一部分，并被认为是刺猬蛋白的共受体。我们已经表达和纯化了Hedgehog、Ihog、Cdo、Boc、磷脂酰肌醇蛋白聚糖和Gas 1蛋白的活性片段，确定了Hh：Ihog、Hh：Cdo和Hh：Boc复合物的晶体结构，并证明了这些相互作用依赖于包括肝素和Ca 2+在内的其他辅因子。我们最近还表达和纯化了少量（~40 μ g）的Patched。为了研究刺猬信号传导的分子机制，并在分子水平上了解刺猬受体的性质，我们建议对这些Hh通路组分及其复合物进行X射线晶体学，生物物理学和生物化学研究。这些研究将阐明Hedgehog信号通路活性的分子机制，从而阐明产生复杂组织模式的分子策略。这些研究也可能揭示分子相互作用或过程，可能是针对治疗抑制刺猬信号。我们将通过以下具体目标实现这些目标：（1）确定磷脂酰肌醇蛋白聚糖调节脊椎动物和无脊椎动物Hedgehog信号传导的分子机制，（2）确定Gas 1调节脊椎动物Hedgehog信号传导的分子机制以及Gas 1与其他Hedgehog信号传导调节剂之间的相互作用，和（3）通过在体外用纯化的组分重构最小Hedgehog结合复合物来确定脊椎动物和无脊椎动物Hedgehog受体复合物的性质。