INTEGRAL MEMBRANE ENZYMES IN ESTROGEN BIOSYNTHESIS

雌激素生物合成中的整体膜酶

• 批准号: 7598554
• 负责人: DEBASHIS GHOSH
• 金额: $ 0.64万
• 依托单位: CORNELL UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-07-01 至 2008-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7598554
• 关键词: Affinity; Anabolism; Androstenedione; Aromatase; Breast Carcinoma; Complex; Computer Retrieval of Information on Scientific Projects Database; Cytochrome P450; Data; Endoplasmic Reticulum; Enzymes; Estrogens; Estrone; Funding; Grant; Hormones; Human; Institution; Integral Membrane Protein; Length; Membrane; Placenta; Prevention; Research; Research Personnel; Resources; Source; Steroids; Steryl-sulfatase; Structure; Sulfatases; Time; United States National Institutes of Health; X ray diffraction analysis; X-Ray Diffraction; inhibitor/antagonist; research study; small molecule

This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. Human steroid (Estrone/DHEA) sulfatase (STS) and cytochrome P450 aromatase (P450arom), two integral membrane proteins of the endoplasmic reticulum, catalyze biosynthesis of the active estrogens. Selective inhibition of one or more of these enzymes by high affinity, highly specific small molecule inhibitors could provide an effective means of prevention and treatment of hormone-dependent breast carcinoma. The plan is to gather X-ray diffraction data on newly grown crystals of inhibited complexes of STS. Recently, we have for the first time grown large single crystals of androstenedione-complex of the full-length P450arom, also purified from human placenta. With CHESS beam time, we plan to conduct cryo-protection optimization experiments and collect diffraction data for solving the crystal structure.

这个子项目是许多研究子项目中的一个 由NIH/NCRR资助的中心赠款提供的资源。子项目和 研究者（PI）可能从另一个NIH来源获得了主要资金， 因此可以在其他CRISP条目中表示。所列机构为 研究中心，而研究中心不一定是研究者所在的机构。 人甾体（雌酮/脱氢表雄酮）硫酸酯酶（STS）和细胞色素P450芳香化酶（P450 arom）是内质网中两种重要的膜蛋白，催化活性雌激素的生物合成。 通过高亲和力、高特异性的小分子抑制剂选择性抑制这些酶中的一种或多种，可以提供预防和治疗乳腺癌依赖性乳腺癌的有效手段。 计划是收集新生长的STS抑制复合物晶体的X射线衍射数据。 最近，我们首次生长了全长P450 arom的雄烯二酮复合物的大单晶，也是从人胎盘中纯化的。 利用CHESS光束时间，我们计划进行低温保护优化实验，并收集衍射数据以解决晶体结构。