Capture the Inhibitor: Affinity Approaches to the Discovery of Secretase Leads

捕获抑制剂：发现分泌酶先导物的亲和方法

• 批准号: 8434860
• 负责人: Philip Williams
• 金额: $ 26.48万
• 依托单位: UNIVERSITY OF HAWAII AT MANOA
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-04-01 至 2015-03-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8434860
• 关键词: Address; Affinity; Alzheimer' s Disease; Amyloid; Amyloid beta-Protein; Amyloid beta-Protein Precursor; Biochemical; Biological; Biological Assay; Biological Factors; Blood - brain barrier anatomy; Cade; Chemical Structure; Chemicals; Complement; Complex; Complex Mixtures; Data; Development; Disease; Disease Progression; Drug Targeting; Eligibility Determination; Enzymes; Etiology; Evaluation; Goals; Impaired cognition; Industry; Lead; Libraries; Link; Marines; Medical; Oceans; Outcomes Research; P-Glycoprotein; Patients; Peptide Hydrolases; Permeability; Pharmaceutical Preparations; Production; Protocols documentation; Research; Series; Solutions; Source; Therapeutic; Work; base; beta-site APP cleaving enzyme 1; chemical resource; cytotoxicity; design; drug development; drug discovery; inhibitor/antagonist; innovation; marine natural product; meetings; neurotoxic; novel; polypeptide; public health relevance; screening; secretase; small molecule

DESCRIPTION (provided by applicant): The formation of oligomers of amyloid-beta is one of the critical factors in the development of Alzheimer's disease, according to the Amyloid Cascade Hypothesis. Drugs that can effectively inhibit A2 production and thus reduce the amount of aggregation would benefit millions of patients world-wide. Ultimately, accessing novel chemical diversity, which complements existing screening libraries, may be the key to unlocking these treatments. Our long-term goal therefore is to discover new drug-like small molecules from marine sources that can be used for the treatment of Alzheimer's disease or as biochemical probes to further our under- standing of the development of this disorder. The objective of this proposal, which is our next step in pursuit of that goal, is to identify these lead compounds using a new screening protocol that will rapidly link a spe- cific compound in a mixture to the observed biological effect without requiring laborious bioassay guided isolation (Aim 1). Rigorous biological evaluation of the inhibitors will identify the best lead (Aim 2). This pro- posal is innovative because it addresses the fundamental barrier in natural products of how to link chemical structure to activity in a new way and applies this solution to the problem of Alzheimer's drug discovery. The specific aims of the proposal are: 1. To identify inhibitors of 2-secretase (BACE1) using an innovative protocol that rapidly links a specific compound within a mixture to the observed biological activity using a new LC-MS homogenous affinity assay. 2. To evaluate the potential of the new inhibitors as BACE1 leads using a gauntlet of assays designed to identify the best candidate. We expect to identify structurally unprecedented classes of BACE1 inhibitors. These new classes of poten- tial anti-Alzheimer drug leads will be evaluated in a series of biochemical assays to assess parameters criti- cal to CNS drug development. A limited number of compounds that meet these requirements will be ad- vanced to further studies in partnership with industry. If successful, the newly discovered leads are ex- pected to have a positive impact by finally validating BACE1 as a drug target, validating the Amyloid Cas- cade Hypothesis and providing desperately needed therapeutics for Alzheimer's patients.

描述(申请人提供)：根据淀粉样级联假说，淀粉样β蛋白低聚体的形成是阿尔茨海默病发展的关键因素之一。能够有效抑制A2产生从而减少聚集量的药物将使全球数百万患者受益。最终，获得新的化学多样性，这是对现有筛选文库的补充，可能是解锁这些治疗的关键。因此，我们的长期目标是从海洋来源中发现新的类似药物的小分子，这些小分子可用于治疗阿尔茨海默病或用作生化探针，以进一步了解这种疾病的发展。这项提议的目标，也是我们追求这一目标的下一步，是使用一种新的筛选方案来鉴定这些先导化合物，该方案将迅速将混合物中的特定化合物与观察到的生物效应联系起来，而不需要费力的生物测定引导分离(目标1)。对抑制剂进行严格的生物学评估将确定最佳铅(目标2)。这种正态是创新的，因为它解决了天然产品中如何以一种新的方式将化学结构与活性联系起来的根本障碍，并将这种解决方案应用于阿尔茨海默氏症的药物发现问题。该提案的具体目标是：1.使用一种创新的方法识别2-分泌酶抑制剂(BACE1)，该方法利用一种新的LC-MS均相亲和分析将混合物中的特定化合物与观察到的生物活性快速联系起来。2.使用一系列旨在确定最佳候选者的测试来评估新抑制剂作为BACE1先导的潜力。我们希望鉴定出结构上前所未有的BACE1抑制剂类别。这些新型潜在的抗阿尔茨海默病药物先导将在一系列生化分析中进行评估，以评估对中枢神经系统药物开发至关重要的参数。符合这些要求的有限数量的化合物将被推进到与工业合作的进一步研究中。如果成功，预计新发现的线索将产生积极影响，最终证实BACE1作为药物靶点，证实淀粉样蛋白Cas-Cade假说，并为阿尔茨海默氏症患者提供急需的治疗药物。