Computational Studies of Model Systems for Protein Unfolded States

蛋白质未折叠状态模型系统的计算研究

• 批准号: 7216738
• 负责人: CARLOS SIMMERLING
• 金额: $ 22.1万
• 依托单位: STATE UNIVERSITY NEW YORK STONY BROOK
• 依托单位国家: 美国
• 财政年份: 2000
• 资助国家: 美国
• 起止时间: 2000-06-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7216738
• 关键词: Address; Adopted; Affect; Alanine; Algorithms; Amber; Area; Biological Models; Boxing; Chemicals; Collaborations; Communities; Complex; Condition; Coupled; Couples; Data; Development; Disease; Elements; Entropy; Equation; Event; Experimental Models; Feedback; Free Energy; Generations; Glycine; Helix (Snails); Human; Hybrids; Hydrogen Bonding; Hydrophobic Interactions; Investigation; Ions; Joints; Kinetics; Measurement; Measures; Methods; Modeling; Molecular Conformation; Mutation; Nature; Numbers; Peptides; Performance; Phase; Physiological; Plant Roots; Population; Principal Investigator; Proline; Property; Proteins; Publishing; Range; Rate; Research; Research Personnel; Residual state; Resolution; Role; Sampling; Simulate; Solvents; Specific qualifier value; Speed; Standards of Weights and Measures; Structure; Study models; System; Techniques; Temperature; Testing; Thermodynamics; Thinking; Time; Validation; Vertebral column; Weight; Work; alanylproline; base; chemical stability; computer studies; cost; ear helix; improved; insight; mutant; novel; novel strategies; particle; polypeptide; programs; prolylglycine; protein folding; research study; simulation; single molecule; size; success; theories; tool

DESCRIPTION (provided by applicant): While unfolded states of proteins were previously thought to be largely random, evidence of specific structure is accumulating. Even at low populations this type of ordering could have direct bearing on protein stability, folding mechanism, and rate, as well as the misfolding and aggregation that are implicated in many human disorders. In most cases, the weak nature of the residual structure and low populations of misfolded states under physiological conditions preclude direct and detailed characterization of these ensembles using experimental techniques. Simulations have begun to provide data complementary to experiments, since they can provide structural detail with single molecule resolution on a time scale inaccessible to most experiments. However, simulations fail in many important cases for multiple reasons. This proposal outlines continued development of simulation algorithms and force fields to enable successful application to the study of unfolded states, with direct validation against experimental data obtained through established collaborations. A strong emphasis is placed on conformational sampling; a major component of the project involves development of a novel sampling approach that provides improved convergence of ensemble data with explicit inclusion of solvent at a significantly reduced computational cost. Simulations will be performed on several model systems of varying complexity. In each case, specific mutations will probe interactions that are hypothesized to be involved in determining the structure or stability of the native fold. Other mutants probe the effect on stability of interactions that we have observed in the unfolded state. These studies will provide useful insight into these important model systems, and will also provide valuable and critical feedback on the performance of our force fields and sampling methods. The next phase of the research involves characterization of unfolded ensembles for each model system, and generation of experimentally testable hypotheses about the nature of any residual structure. For each of the model systems, recent experiments suggest that residual structure may exist in the unfolded state, and our simulations will provide important models for interpretation of this data. Additional studies of the unfolded state and the role of entropy in folding will be performed through replacement of flexible glycine and rigid proline with alanine, investigating the effect on unfolded state entropy and free energy of folding.

描述(申请人提供)：虽然以前认为蛋白质的展开状态在很大程度上是随机的，但特定结构的证据正在积累。即使在低种群中，这种类型的排序也可能直接影响蛋白质的稳定性、折叠机制和速率，以及与许多人类疾病有关的错误折叠和聚集。在大多数情况下，残基结构的弱性质和生理条件下错误折叠状态的低种群排除了使用实验技术直接和详细地描述这些系综的可能性。模拟已经开始为实验提供补充数据，因为它们可以在大多数实验无法获得的时间尺度上提供单分子分辨率的结构细节。然而，由于多种原因，模拟在许多重要情况下都会失败。该提案概述了模拟算法和力场的持续发展，以使其能够成功地应用于展开状态的研究，并根据通过已建立的合作获得的实验数据进行直接验证。该项目的一个主要组成部分是开发一种新的采样方法，该方法通过显式包含溶剂来改进集合数据的收敛，同时大大降低计算成本。将在不同复杂性的几个模型系统上进行仿真。在每种情况下，特定的突变都会探测到被假设参与决定天然折叠的结构或稳定性的相互作用。其他突变体探测我们在未折叠状态下观察到的相互作用稳定性的影响。这些研究将为这些重要的模型系统提供有用的见解，并将就我们的力场和采样方法的表现提供有价值的和关键的反馈。下一阶段的研究包括描述每个模型系统的展开系综，以及生成关于任何剩余结构的性质的可实验验证的假设。对于每个模型系统，最近的实验表明，在展开状态下可能存在剩余结构，我们的模拟将为解释这一数据提供重要的模型。通过用丙氨酸取代柔性甘氨酸和刚性脯氨酸，进一步研究折叠中的未折叠状态和熵在折叠中的作用，考察它们对折叠的未折叠状态和自由能的影响。