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Visualizing Actomyosin Transients by Data Merging

通过数据合并可视化肌动球蛋白瞬变

基本信息

批准号：
7725764
负责人：
Thomas P Burghardt
金额：
$ 32.39万
依托单位：
MAYO CLINIC ROCHESTER
依托单位国家：
美国
项目类别：
财政年份：
2004
资助国家：
美国
起止时间：
2004-04-01 至 2014-06-30
项目状态：
已结题

来源：
https://reporter.nih.gov/project-details/7725764
关键词：
ATP Hydrolysis ATP phosphohydrolase ATP-G-actin Abbreviations Actins Active Sites Actomyosin Address Affect Amino Acid Substitution Amino Acids Aorta Area Binding Binding Sites Biological Assay Cardiac Chemicals Chickens Circular Dichroism Coupled Coupling Data Dictyostelium discoideum Disease Etiology Exercise Physiology F-Actin Fluorescence Fluorescence Microscopy Fluorescent Probes Free Energy Freedom Goals Green Fluorescent Proteins H-Meromyosin Head Human Label Lead Learning Life Light Link Lysine Mediating Methods Metric Microfilaments Microscopy Mining Modeling Modification Molecular Conformation Molecular Motors Motor Movement Muscle Mutagenesis Mutation Myopathy Myosin ATPase Myosin Heavy Chains Myosin Light Chain Kinase Myosin Light Chains Myosin Regulatory Light Chains Myosin S-1 Nucleotides Occupations Pathology Pathway interactions Peptides Phenotype Play Population Positioning Attribute Power stroke Probability Productivity Protein Isoforms Proteins Recombinant Proteins Relative (related person)Research Resolution Rhodamine Rhodamines Role Rotation Shapes Site Smooth Muscle Myosins Sorting - Cell Movement Source Structure Surface System Techniques Testing Thermodynamics Time Translating Translations Tryptophan Upper arm Variant Work acronyms analytical tool base cell motility density design human disease in vitro Assay insight molecular dynamics mutant nanometer next generation public health relevance repaired sensor simulation skeletal transmission process

项目摘要

DESCRIPTION (provided by applicant): Myosin is a molecular motor binding ATP and actin to produce work by causing relative translation of the two proteins. Myosin contains a lever arm probably executing a power stroke by rotating through an angle of ~70o to translate actin against resistive force. ATP hydrolysis at myosin's active site energizes contraction by influencing lever arm movement and is influenced by allostery with actin in actin-activation of myosin ATPase. The influences are conducted through the protein matrix by coupling pathways investigated by mutation (naturally occurring and computation inspired), molecular dynamics simulation (MD), and structure/function assays. Two coupling pathways identified for study mediate actin-activation of myosin ATPase and conformation change triggering tryptophan nucleotide sensitivity that might link small active site displacements to the larger lever arm movement. The goal of the project is to elucidate the native relationships among actin binding, active site conformation, lever arm rotation and protein displacement and then to observe how these relationships are affected by modifications introduced to coupling pathways. Human skeletal myosin variants play a fundamental role in exercise physiology, human disease, and population diversity. The variants involve widely dispersed amino acid substitutions covering several regions essential to function and are naturally embedded clues to discovering functional domain interconnectedness through the coupling pathways. They implicate sites for mutagenesis in model proteins and are essential for correlation of myosin functional alteration to phenotype. Myosin MD simulation provides complementary insights into how coupling pathways perform. MD introduces the causality test identifying source, path, and termination of coupling networks in sequential time that is an integral part of the competent motor. Causality testing applied to tryptophan nucleotide sensitivity has converged with experimental findings from a tonic smooth muscle myosin to suggest tryptophan nucleotide sensitivity could disconnect from lever arm movement in native myosin. A new experimental causal rotation/displacement metric, quantifying completion of a productive myosin cycle, will correlate myosin lever arm rotation with displacement of a bound actin filament (F-actin) in an in vitro assay. The two-molecule technique utilizes a green fluorescent protein (GFP) on myosin and nanometer resolution localization of a fluorescent probe bound to F-actin. Myosin variants that are, adapted to specialize function, implicated in human disease, or sourced in population diversity, are mined for insight into functional divergence. MD simulation introduces causality to characterize myosin coupling networks and produces experimentally testable hypotheses. A causal two-molecule assay tests completion of a productive myosin cycle and characterizes myosin's ability to displace actin. These analytical tools are next-generation methods addressing transduction and motility in muscle myosin. PUBLIC HEALTH RELEVANCE: Skeletal myosin is the motor in muscle powering contraction. Its ability to convert chemical energy to useful movement is fundamental to our ability to lead happy and productive lives. The proposed research promotes understanding of its design for energy conversion shaping approaches for how to repair an ailing motor and how to adapt it to applications where muscle productivity is limiting human potential.

描述（由申请人提供）：肌凝蛋白是一种结合ATP和肌动蛋白的分子马达，通过引起两种蛋白质的相对翻译来产生工作。肌凝蛋白包含一个杠杆臂，可能通过旋转约70度的角度来执行动力冲程，以使肌动蛋白对抗阻力。肌凝蛋白活性部位的ATP水解通过影响杠杆臂运动而激活收缩，并受肌动蛋白激活肌凝蛋白ATP酶的变构影响。影响是通过突变（自然发生和计算启发）、分子动力学模拟（MD）和结构/功能分析研究的偶联途径通过蛋白质基质进行的。研究中确定的两种偶联途径介导肌动蛋白-肌球蛋白atp酶的激活和引发色氨酸核苷酸敏感性的构象改变，这可能将小的活性位点位移与较大的杠杆臂运动联系起来。该项目的目标是阐明肌动蛋白结合、活性位点构象、杠杆臂旋转和蛋白质位移之间的天然关系，然后观察这些关系如何受到引入偶联途径的修饰的影响。人类骨骼肌球蛋白变异在运动生理学、人类疾病和种群多样性中发挥着重要作用。这些变异涉及广泛分散的氨基酸取代，覆盖了几个功能必需的区域，并且是通过偶联途径发现功能域互连性的自然嵌入线索。它们涉及模型蛋白的突变位点，并且对肌球蛋白功能改变与表型的相关性至关重要。肌球蛋白MD模拟提供了对耦合途径如何执行的补充见解。MD介绍了因果关系测试识别源，路径，并在连续时间耦合网络的终止，这是一个组成部分的主管电机。应用于色氨酸核苷酸敏感性的因果关系测试与强直性平滑肌肌球蛋白的实验结果一致，表明色氨酸核苷酸敏感性可能与天然肌球蛋白的杠杆臂运动脱节。一种新的实验性因果旋转/位移度量，量化生产肌凝蛋白周期的完成，将肌凝蛋白杠杆臂旋转与结合的肌动蛋白丝（F-actin）的位移在体外分析中联系起来。两分子技术利用绿色荧光蛋白（GFP）在肌球蛋白和纳米分辨率定位荧光探针结合到f -肌动蛋白。肌凝蛋白的变异，适应专门的功能，涉及人类疾病，或来源的群体多样性，挖掘洞察功能差异。MD模拟引入因果关系来表征肌球蛋白耦合网络，并产生可实验验证的假设。因果双分子分析测试完成生产肌凝蛋白周期和表征肌凝蛋白的能力取代肌动蛋白。这些分析工具是解决肌球蛋白转导和运动的下一代方法。公共卫生相关性：骨骼肌球蛋白是肌肉动力收缩的动力。它将化学能转化为有用运动的能力是我们过上幸福和富有成效生活的基础。拟议的研究促进了对其能量转换设计的理解，形成了如何修复病态马达的方法，以及如何使其适应肌肉生产力限制人类潜力的应用。