Multiscale modeling of mechanisms for viral capsid assembly and polymorphism

病毒衣壳组装和多态性机制的多尺度建模

• 批准号: 7989140
• 负责人: MICHAEL F HAGAN
• 金额: $ 22.66万
• 依托单位: BRANDEIS UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2008
• 资助国家: 美国
• 起止时间: 2008-12-01 至 2013-11-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7989140
• 关键词: Antiviral Agents; Base Pairing; Capsid; Capsid Proteins; Cells; Cereals; Charge; Collaborations; Computer Simulation; Data; Drug Delivery Systems; Drug resistance; Essential Amino Acids; Event; Genetic Polymorphism; Goals; Harvest; Health; Image; Infection; Kinetics; Lead; Learning; Length; Light; Modeling; Molecular Conformation; Morphology; Mutate; Nature; Nucleic Acids; Organism; Pharmaceutical Preparations; Polymers; Process; Property; Protein Conformation; Protein Subunits; Proteins; RNA; Reaction; Research; Resistance; Resolution; Sampling; Site; Structure; Study models; System; Viral; Viral Proteins; Virus; Virus Diseases; Water; Work; base; conformational conversion; cowpea chlorotic mottle virus; density; driving force; experience; fighting; forging; multi-scale modeling; multiple drug use; nanoparticle; novel; polyanion; research study; simulation

DESCRIPTION (provided by applicant): During the replication of many viruses, hundreds to thousands of protein subunits assemble around the viral nucleic acid to form a protein shell called a capsid. Within their host organism, most viruses form one particular structure with astonishing fidelity; yet, recent experiments demonstrate that capsids can assemble with different sizes and morphologies to accommodate nucleic acids, inorganic nanoparticles, and polyanions with different sizes. This project will use computational models to determine the features of viral proteins and their cargoes that enable assembly to be so precise and yet so adaptable. We develop simplified representations of viral proteins and cargoes that range from rigid spheres to fluctuating polymers to model nucleic acids. With these models we will develop experimentally testable predictions for the mechanisms by which viral proteins dynamically encapsidate these objects, and which factors direct the assembly process towards a particular size and morphology. These coarse-grained models of the overall assembly process will be validated and guided by atomic-resolution simulations that examine the dynamic conformations of viral proteins. PUBLIC HEALTH RELEVANCE: Viral diseases and acquired drug resistance by viruses are major biomedical challenges. The most effective antiviral treatments fight acquired resistance by using use multiple drugs to target several steps in the infection process, but relatively few treatments target viral assembly. By identifying the features that make viral assembly successful, we can learn to block it and thereby create novel antivirus therapies.

描述（由申请人提供）：在许多病毒的复制过程中，数百至数千个蛋白质亚基围绕病毒核酸组装，形成称为衣壳的蛋白质外壳。大多数病毒在其宿主生物体内以惊人的保真度形成一种特定的结构;然而，最近的实验表明，衣壳可以组装成不同的大小和形态，以容纳不同大小的核酸，无机纳米颗粒和聚阴离子。该项目将使用计算模型来确定病毒蛋白质及其货物的特征，这些特征使组装变得如此精确且适应性如此强。我们开发了病毒蛋白质和货物的简化表示，从刚性球体到波动聚合物到模型核酸。有了这些模型，我们将开发实验可测试的预测机制，病毒蛋白质的动态adminsidate这些对象，哪些因素直接组装过程中对一个特定的大小和形态。这些粗粒度的模型的整个组装过程将验证和指导原子分辨率的模拟，检查病毒蛋白质的动态构象。公共卫生相关性：病毒性疾病和病毒获得性耐药性是主要的生物医学挑战。最有效的抗病毒治疗通过使用多种药物靶向感染过程中的几个步骤来对抗获得性耐药性，但相对较少的治疗针对病毒组装。通过识别使病毒组装成功的特征，我们可以学会阻止它，从而创造新的抗病毒疗法。