Protein Dynamics in Homeodomain/DNA Complexes

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，尚未完全理解。特别是，我们对分子动力学在蛋白质/DNA相互作用中所起作用的知识和理解存在着关键和实质性的差距。分子识别领域的一个普遍问题是，结构研究对络合物形成的自由能的熵分量的揭示相对较少。因此，通过开展旨在阐明蛋白质/DNA界面中构象动力学的性质和贡献的细节的研究来补充现有的结构信息是非常重要的。我们建议使用溶液态核磁共振光谱来表征蛋白质/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，它被定义为那些在DNA识别螺旋的第50位有赖氨酸残基的同源结构域。同源结构域基序一直是表征蛋白质/DNA相互作用的一个非常重要的模型系统，同源结构域与DNA相互作用的功能和结构研究提供了丰富的信息。这些结构研究已经证明了一个保守的全局折叠和对接排列，但关于关键氨基酸残基在蛋白质- dna界面上的作用以及侧链运动的程度和意义的基本问题仍然存在。所提出的研究的一般假设是，蛋白质侧链动力学的调节（而不是固定）在以下方面起着重要作用：(1)在DNA和同源DNA结合蛋白之间建立互补界面；(2)允许给定的DNA结合蛋白识别一致和非一致的DNA序列。该项目的具体目标是：(1)确定与含有共识结合位点TAATCC的DNA双工结合的果蝇Bicoid蛋白同源结构域的侧链动力学；(2)确定与非一致DNA位点结合的Bicoid同源结构域的侧链动力学；(3)确定Pitx2同源结构域/DNA复合物的结构和动力学。每一个特定的目标都需要同源结构域/DNA复合物的结构测定；到目前为止，还没有k50级同域结构的报道。显然，同域模型不能完全代表所有的蛋白质/DNA相互作用。然而，本文提出的蛋白质动力学的综合研究将有助于建立一个知识基础，在此基础上，未来的工作可以建立在蛋白质运动的性质及其在蛋白质/DNA识别中的意义上。

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.