Impact of naturally occurring osmolytes on protein structure and energetics

天然存在的渗透剂对蛋白质结构和能量学的影响

• 批准号: 7392399
• 负责人: Jorg Rosgen
• 金额: $ 31.02万
• 依托单位: UNIVERSITY OF TEXAS MED BR GALVESTON
• 依托单位国家: 美国
• 财政年份: 1993
• 资助国家: 美国
• 起止时间: 1993-08-01 至 2010-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7392399
• 关键词: Affect; Behavior; Biochemistry; Biological; Biophysics; Brain; Brain Edema; Cell Volumes; Cell physiology; Cells; Chemicals; Clinical; Companions; Complex; Condition; Couples; Crystallization; Cystic kidney; Cytoplasm; Depth; Diabetes Mellitus; Disease; Drug Formulations; Drug Industry; Foundations; Free Energy; Goals; Hand' s disease; Health; Hydration status; Investigation; Kidney; Knowledge; Lead; Measurement; Measures; Mediating; Methods; Microscopic; Molecular; Molecular Chaperones; Nature; Organ; Organism; Outcome; Pathology; Peptides; Pharmaceutical Preparations; Pharmacologic Substance; Play; Polycystic Kidney Diseases; Positioning Attribute; Process; Property; Proteins; Range; Regulation; Relative (related person); Research; Research Personnel; Role; Side; Sodium Chloride; Solutions; Solvents; Stress; Structure; System; Thermodynamics; Thinking; Tissues; Urea; Vaccines; Vertebral column; Water; Work; antidiuresis; base; biological adaptation to stress; brain cell; coping; glucosyltransferase E; kidney cell; kidney medulla; macromolecule; practical application; preference; present value; pressure; prevent; protein folding; protein function; protein protein interaction; protein structure; response

DESCRIPTION (provided by applicant): Protecting osmolytes are responsible for the kidney medulla's extraordinary ability to cope with intracellular urea concentration as high as 1.5M. These small organic molecules are common in cells of many tissues, and an important part of their action in kidney is to stabilize intracellular proteins against the deleterious effects of urea. Besides being essential for our survival, imbalances in osmolyte levels play key roles in such conditions as polycystic kidney disease, diabetes mellitus, and brain edema. Though many biological roles of osmolytes arise from their solvation of proteins, it is unknown how protein solvation facilitates these roles. This gap in knowledge prevents a complete understanding of osmolyte effects and their roles in normal and disease states. Our long-term goal is to understand how interactions among osmolytes, water, and biomolecules give rise to osmotic stress response on the one hand, and disease on the other. Using measurements of the transfer free energy of protein side-chain and peptide backbone groups (GTFEs) from water to osmolyte solution, we recently made the remarkable discovery of how to predict the energetics of protein-stability in osmolytes. Our aims are to consolidate and use this ability to determine the underlying forces responsible for protein stability, and to the predict energetic effects of osmolytes on contraction and accretion of structure in denatured ensembles. We will extend our use of GTFEs to enable predictions of protein-protein interaction free energies, to better understand how fluctuating osmolyte concentrations affect key protein-protein interactions vital to cellular responses, and determine the extent to which kidney osmolytes act synergistically, negatively, or independently in affecting the properties of proteins. We aim to merge our ability to predict the energetics of protein stability and solvation effects with Kirkwood-Buff approaches that structurally relate water*osmolyte*protein interaction with the energetics, to give a considerably more detailed mechanistic understanding of protein solvation than currently exists. Relevance: This project will lead to a better understanding of how osmolytes protect proteins from unfolding under harsh condition, and how imbalances in osmolyte levels can contribute to the pathology of such conditions as polycystic kidney disease, diabetes mellitus, and brain swelling. Our work will have practical applications in the pharmaceutical industry for stabilization of vaccines and protein/ peptide drugs.

描述（由申请人提供）：肾髓质具有非凡的能力来应对高达1.5M的细胞内尿素浓度，保护渗透细胞负责。这些小的有机分子在许多组织的细胞中都很常见，它们在肾脏中的一个重要作用是稳定细胞内蛋白，抵抗尿素的有害作用。除了对我们的生存至关重要外，渗透液水平的不平衡在多囊肾病、糖尿病和脑水肿等疾病中起着关键作用。虽然渗透细胞的许多生物学作用来自于它们对蛋白质的溶剂化，但蛋白质溶剂化如何促进这些作用尚不清楚。这种知识上的差距阻碍了对渗透作用及其在正常和疾病状态下的作用的全面理解。我们的长期目标是了解渗透物、水和生物分子之间的相互作用如何一方面引起渗透应激反应，另一方面引起疾病。通过测量蛋白质侧链和肽主链（gtfe）从水到渗透溶液的转移自由能，我们最近在如何预测渗透溶液中蛋白质稳定性的能量学方面取得了显著的发现。我们的目标是巩固和利用这种能力来确定负责蛋白质稳定性的潜在力量，并预测渗透物对变性整体结构收缩和增加的能量效应。我们将扩展gtfe的使用，以预测蛋白质-蛋白质相互作用的自由能，更好地理解渗透液浓度的波动如何影响对细胞反应至关重要的关键蛋白质-蛋白质相互作用，并确定肾脏渗透液在影响蛋白质特性方面的协同作用、负作用或独立作用的程度。我们的目标是将我们预测蛋白质稳定性和溶剂化效应的能量学的能力与Kirkwood-Buff方法结合起来，这种方法在结构上将水*渗透物*蛋白质相互作用与能量学联系起来，从而对蛋白质溶剂化提供比目前存在的更详细的机制理解。相关性：该项目将有助于更好地了解渗透蛋白如何在恶劣条件下保护蛋白质免遭展开，以及渗透蛋白水平失衡如何导致多囊肾病、糖尿病和脑肿胀等疾病的病理。我们的工作将在稳定疫苗和蛋白质/肽药物的制药工业中有实际应用。