Structural Studies of Metabolic Membrane Proteins

描述（由申请人提供）：我们获得了参与细菌甘油代谢途径的两种膜蛋白的衍射晶体，即甘油促进剂和甘油-3-磷酸脱氢酶。这是晶体结构测定的重要一步，这些结构将产生有价值的新见解，将蛋白质折叠与功能和蛋白质-蛋白质相互作用以及溶质分子的催化，调节和跨膜摄取机制联系起来。细菌增殖的潜在有效机制是介导氧化和碳水化合物代谢的手段。这种结构研究的重点是阐明介导基本氧化和碳水化合物代谢的关键细菌膜蛋白的结构-功能关系。我们已经从事这些代谢蛋白质的结构研究多年，并且处于将我们所有的结果整合到这些致病细菌代谢的全面和连贯的图片中的关键点。我们已经确定了氧化和甘油代谢途径的其他三个成员的结构，包括NADH过氧化物酶，NADH氧化酶和甘油激酶。这一建议涉及结构与功能和监管之间的关键问题。Gly-3-磷酸脱氢酶具有特别的医学重要性，因为它是提供用于生物合成多糖的磷酸丙糖中间体的关键参与者，所述多糖形成生物膜并保护细菌免于脱水以及抗生素治疗。这种膜蛋白结构研究有可能产生新的和新颖的结果，这是不提供高通量结构基因组学。我们已经克服了一些最困难的和限速的障碍，在膜蛋白结构的研究，获得衍射晶体的甘油促进剂（2.4 A）从革兰氏阳性肺炎链球菌，膜蛋白参与甘油摄取和可能通过蛋白质-蛋白质相互作用与甘油激酶，其结构，我们最近确定的调节。这与革兰氏阴性大肠杆菌之间存在细微但显著的差异。大肠杆菌易化因子。我们有来自铜绿假单胞菌的甘油-3-磷酸脱氢酶（3.3 A）的衍射晶体，并有希望获得更好的衍射晶体。我们的具体目标是获得两种膜蛋白的原子分辨率结构，这两种膜蛋白都可能成为抗生素设计和治疗的新靶点。

DESCRIPTION (provided by applicant): We have obtained diffracting crystals of two membrane proteins involved in the glycerol metabolic pathway in bacteria, glycerol facilitator and glycerol-3-phosphate dehydrogenase. This is a significant step towards crystal structure determination and these structures will yield valuable new insight, linking protein folds to function and protein-protein interactions as well as mechanisms of catalysis, regulation, and transmembrane uptake of solute molecules. Underlying effective mechanisms of bacterial proliferation are means of mediating oxidative and carbohydrate metabolism. This structural study focuses on elucidating structure-function relationships of key bacterial membrane proteins that mediate fundamental oxidative and carbohydrate metabolism. We have been engaged in structural studies of these metabolic proteins for several years and are at pivotal point in integrating all of our results into a comprehensive and coherent picture of metabolism in these pathogenic bacteria. We have determined the structures of three other members of the oxidative and glycerol metabolism pathways, including NADH peroxidase, NADH oxidase, and glycerol kinase. This proposal addresses key questions correlating structure to function and regulation. Gly-3-phosphate dehydrogenase is of particular medical importance as it is a key player in providing triose phosphate intermediates for biosynthesis of polysaccharides that form biofilm and protects the bacterium from dehydration as well as antibiotic therapy. This membrane-protein structural study has the potential to yield new and novel results, which are not provided by high-throughput structural genomics. We have overcome some of the most difficult and rate-limiting hurdles in membrane protein structural studies by obtained diffracting crystals of the glycerol facilitator (2.4 A) from Gram-positive Streptococcus pneumonia, a membrane protein involved in glycerol uptake and likely to be regulated via protein-protein interactions with glycerol kinase, whose structure we've recently determined. Subtle but significant differences exist between this and the Gram-negative E. coli facilitator. We have diffracting crystals of the glycerol-3-phosphate dehydrogenase (3.3 A) from Pseudomonas aeruginosa and have promising indications for better diffracting crystals. Our specific aims are to obtain atomic resolution structures of both membrane proteins, both of which are likely to be novel targets for antibiotic design and therapy.