在基于结构的药物设计中探索多种蛋白质构造的实验来源
Kelly L Damm1, Heather A Carlson
1Department of Medicinal Chemistry, University of Michigan, Ann Arbor, MI 48109-1065, USA.
Journal of the American Chemical Society
|June 9, 2007
概括
结合蛋白质灵活性,使用多种构造来改进药物设计. 在基于结构的药物设计中,NMR组合比晶体结构提供了更普遍和更准确的活性位点表示.
科学领域:
- 结构生物学是结构生物学.
- 计算化学是一种计算化学.
- 药物发现 药物发现
背景情况:
- 蛋白质的灵活性对于准确的基于结构的药物设计至关重要.
- 之前的工作使用了计算机生成的形状,用于人类免疫缺陷病毒-1蛋白酶 (HIV-1p) 药模型.
研究的目的:
- 为了比较NMR合并与晶体结构的实用性,用于生成多重蛋白结构 (MPS) 药模型.
- 评估蛋白质灵活性对基于结构的HIV-1p药物设计的影响.
主要方法:
- 使用NMR组合和HIV-1p的晶体结构集合生成了MPS药模型.
- 将这些模型的性能与从单个蛋白质构造得出的模型进行了比较.
- 评估模型区分已知的抑制剂与诱分子的能力.
主要成果:
- 基于NMR组合和基于晶体结构的MPS模型都成功区分了HIV-1p抑制剂.
- MPS模型的性能优于单一配置模型.
- 一组NMR组合表现出比一组大型晶体结构更大的结构变化.
- 源自NMR的MPS模型提供了最普遍和最准确的活性位点表示.
结论:
- 多重蛋白质结构药模拟增强了基于结构的药物设计.
- 核磁共振组合对于捕获蛋白质灵活性和生成强大的药物设计模型是有价值的.
- 这项研究倡导在基于结构的药物设计中使用NMR模型.
相关概念视频
Protein Organization
Proteins are polymers of amino acid residues. They are versatile and responsible for different cellular functions, including DNA replication, molecular transport, catalysis, and structural support. Proteins have a hierarchical structure comprising at least three levels of organization: primary, secondary, and tertiary structure. Some large proteins have a quaternary structure where individual protein subunits are linked together.
The primary structure of a protein is its amino acid sequence.
The primary structure of a protein is its amino acid sequence.
Conserved Binding Sites
Many proteins’ biological role depends on their interactions with their ligands, small molecules that bind to specific locations on the protein known as ligand-binding sites. Ligand-binding sites are often conserved among homologous proteins as these sites are critical for protein function.
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Binding sites are often located in large pockets, and if their location on a protein’s surface is unknown, it can be predicted using various approaches. The energetic method computationally analyses the...
Ligand Binding and Linkage
Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked. In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence the...
Protein Folding
Proteins are chains of amino acids linked together by peptide bonds. Upon synthesis, a protein folds into a three-dimensional conformation, critical to its biological function. Interactions between its constituent amino acids guide protein folding, and hence the protein structure is primarily dependent on its amino acid sequence.
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
Protein Structure Is Critical to Its Biological Function
Proteins perform a wide range of biological functions such as catalyzing chemical reactions, providing...
Protein Folding
Overview
Ligand Binding Sites
Proteins are dynamic macromolecules that carry out a wide variety of essential processes; however, the activities of most proteins depend on their interactions with other molecules or ions, known as ligands.
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...
Protein-ligand interactions are quite specific; even though numerous potential ligands surround a cellular protein at any given time, only a particular ligand can bind to that protein. Moreover, a ligand binds only to a dedicated area on the surface of the protein, known as the...


