Protein Dynamics in Homeodomain/DNA Complexes

同源结构域/DNA 复合物中的蛋白质动力学

• 批准号: 7061269
• 负责人: MARK A RANCE
• 金额: $ 28.73万
• 依托单位: UNIVERSITY OF CINCINNATI
• 依托单位国家: 美国
• 财政年份: 2003
• 资助国家: 美国
• 起止时间: 2003-05-01 至 2009-01-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7061269
• 关键词: Affinity; Amino Acids; Binding; Binding Sites; Biochemical; Biological; Biological Models; Cells; Characteristics; Chemicals; Class; Complement; Complex; Condition; Consensus; Consensus Sequence; Covalent Interaction; DNA; DNA Binding; DNA Binding Domain; DNA Sequence; DNA Structure; DNA-Binding Proteins; DNA-Protein Interaction; Data; Development; Docking; Drosophila genus; Foundations; Free Energy; Future; Genes; Genetic Transcription; Goals; Hand; Helix (Snails); Homeodomain Proteins; Human; Immobilization; Knowledge; Life; Light; Lysine; Measures; Mediating; Methodology; Modeling; Motion; NMR Spectroscopy; Nature; Nuclear; Numbers; Participant; Play; Positioning Attribute; Process; Protein Binding; Protein Dynamics; Proteins; Range; Rate; Relaxation; Reporting; Research; Research Design; Rieger syndrome; Roentgen Rays; Role; Role playing therapy; Side; Site; Solutions; Specificity; Stress; Structure; System; Techniques; Testing; Thermodynamics; Vertebral column; Work; X-Ray Crystallography; concept; cost; ear helix; homeodomain; insight; interest; molecular dynamics; molecular recognition; mutant; protein function; protein protein interaction; protein structure; recombinational repair; transcription factor

DESCRIPTION (provided by applicant): Fundamental cellular activities such as the transcription, replication, recombination and repair of genes require the non-covalent interaction of DNA and DNA-binding proteins. The underlying molecular recognition processes governing protein-DNA interactions are complex and not yet fully understood. In particular, critical and substantial gaps exist in our knowledge and understanding of the role played by molecular dynamics in protein/DNA interactions. A general problem in the field of molecular recognition is that structural studies reveal relatively little about the entropic component of the free energy of complex formation. Thus, it is very important to complement available structural information by undertaking studies designed to elucidate details concerning the nature and contributions of conformational dynamics in the protein/DNA interface. We propose to use solution-state NMR spectroscopy to characterize the dynamics of amino acid side chains in model systems of protein/DNA complexes. The model system chosen for study is the so-called K50 class of homeodomain proteins, which is defined as those homeodomains that have a lysine residue at position 50 in the DNA recognition helix. The homeodomain motif has been a very important model system for characterizing protein/DNA interactions, and a wealth of information concerning homeodomain/DNA interactions has been provided by both functional and structural studies. These structural studies have demonstrated a conserved global fold and docking arrangement, but fundamental questions remain concerning the roles of key amino acid residues at the protein-DNA interface and about the extent and significance of side chain motions. The general hypotheses of the proposed research are that modulation (as opposed to immobilization) of protein side chain dynamics plays important roles in (1) establishing a complementary interface between DNA and a cognate DNA-binding protein, and (2) allowing a given DNA-binding protein to recognize consensus and non-consensus DNA sequences. The specific aims of the project are: (1) to determine the side chain dynamics of the homeodomain from the Drosophila Bicoid protein, bound to a DNA duplex containing the consensus binding site TAATCC; (2) to determine the side chain dynamics of the Bicoid homeodomain bound to a non-consensus DNA site; and (3) to determine the structure and dynamics of the Pitx2 homeodomain/DNA complex. Each of these specific aims will require a structure determination of the homeodomain/DNA complex; to date no K50-class homeodomain structure has been reported. Clearly, the homeodomain model cannot be fully representative of all protein/DNA interactions. However, the comprehensive studies of protein dynamics that are proposed herein will help to create a foundation of knowledge upon which future work can build, regarding the nature of protein motions and their significance in protein/DNA recognition.

描述（由申请人提供）：基本的细胞活动，如基因的转录、复制、重组和修复，需要DNA和DNA结合蛋白的非共价相互作用。控制蛋白质-DNA相互作用的潜在分子识别过程是复杂的，并且尚未完全理解。特别是，关键和实质性的差距存在于我们的知识和理解的作用，分子动力学在蛋白质/DNA相互作用。在分子识别领域的一个普遍问题是，结构研究揭示相对较少的熵的复杂形成的自由能的分量。因此，这是非常重要的，以补充现有的结构信息进行研究，旨在阐明有关的性质和贡献的构象动力学在蛋白质/DNA界面的细节。我们建议使用溶液状态NMR光谱来表征蛋白质/DNA复合物模型系统中氨基酸侧链的动力学。选择用于研究的模型系统是所谓的K50类同源结构域蛋白，其被定义为在DNA识别螺旋中的位置50处具有赖氨酸残基的那些同源结构域。同源结构域模体已经成为表征蛋白质/DNA相互作用的一个非常重要的模型系统，功能和结构研究提供了大量关于同源结构域/DNA相互作用的信息。这些结构的研究已经证明了一个保守的全球折叠和对接安排，但基本的问题仍然是关于蛋白质-DNA界面的关键氨基酸残基的作用和侧链运动的程度和意义。所提出的研究的一般假设是，蛋白质侧链动力学的调制（而不是固定）在（1）建立DNA和同源DNA结合蛋白之间的互补界面，以及（2）允许给定的DNA结合蛋白识别共有和非共有DNA序列中起着重要作用。该项目的具体目标是：（1）确定果蝇Bicoid蛋白同源结构域的侧链动力学，该同源结构域与含有共有结合位点TAATCC的DNA双链体结合;（2）确定Bicoid同源结构域与非共有DNA位点结合的侧链动力学;（3）确定Pitx 2同源结构域/DNA复合物的结构和动力学。这些特定目标中的每一个都需要同源结构域/DNA复合物的结构测定;迄今为止，还没有K50类同源结构域结构的报道。显然，同源结构域模型不能完全代表所有蛋白质/DNA相互作用。然而，本文提出的蛋白质动力学的全面研究将有助于建立一个知识的基础上，未来的工作可以建立，关于蛋白质运动的性质及其在蛋白质/DNA识别的意义。