Genetic code expansion for the construction of beyond rule-of-5 compliant macrocyclic peptide libraries

用于构建超五规则合规大环肽库的遗传密码扩展

• 批准号: 10450162
• 负责人: Matthew C Hartman
• 金额: $ 24.87万
• 依托单位: VIRGINIA COMMONWEALTH UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-08-01 至 2025-05-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10450162
• 关键词: Affinity; Amino Acids; Amino Acyl Transfer RNA; Amino Acyl-tRNA Synthetases; Base Pairing; Binding; Biological Assay; Catalogs; Charge; Code; Codon Nucleotides; Collection; Couples; Development; Disease; Diversity Library; Escherichia coli; Future; Genetic Code; Goals; Guidelines; Hydrogen Bonding; In Vitro; Individual; Libraries; Messenger RNA; Methods; Oligonucleotides; Oral; Peptide Library; Peptides; Pharmaceutical Preparations; Positioning Attribute; Proteins; Randomized; Reading; Refractory; Research; Sense Codon; Source; Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization; Structure; Surface; System; Techniques; Technology; Terminator Codon; Testing; Time; Transfer RNA; Translations; Variant; base; drug discovery; experience; experimental study; falls; inhibitor; member; monomer; new technology; peptidomimetics; preference; protein protein interaction; public health relevance; small molecule; success; translation assay

Modified Project Summary/Abstract Section Many intracellular targets involve intracellular protein-protein interactions that are “undruggable” because the binding surfaces are too large and featureless to be blocked by a standard rule-of-5 compliant small molecule. Recently, there have been attempts to catalog molecules that are orally bioavailable but lie beyond the rule of five (bRo5) to access these targets. Macrocyclic peptides can inhabit this bRo5 space, and a key advantage to using peptides as bRo5 molecules is that there are many mature techniques for finding peptide binders from vast libraries. Arguably, the most powerful of these techniques is mRNA display, which allows creation of peptide libraries containing over 10 trillion variants, 6-7 orders of magnitude larger than a standard peptide library prepared on beads. The extreme diversity of these libraries has enabled many successes in inhibitor development. Yet these successes are disconnected from real drug discovery, because the peptides uncovered are much too large to be bRo5 compliant. Libraries that are short in sequence and bRo5 compliant can be created by mRNA display, but these libraries lack the diversity needed to uncover potent inhibitors because standard mRNA display is limited by the genetic code to ~20 variants at each position. In this proposal, strategies to enhance this positional diversity will be pursued. This will first involve breaking the degeneracy of the standard genetic code through isolation of fully modified tRNA isoacceptors. Based on codon reading rules it is predicted that this will allow the addition of 10 non-canonical amino acids (ncAAs) to the code. The second aim focuses on combining these newly defined codon reading rules and previously described tRNAs with unnatural base pairs to allow expansion of the genetic code to the use of 40 monomers at each position. This aim will also focus on developing and testing a curated group of aminoacyl-tRNAs for the future creation of bRo5 compliant libraries containing billions of variants for use in drug discovery.

修改项目摘要/摘要部分 许多细胞内靶点涉及细胞内蛋白质-蛋白质相互作用，这些相互作用是“不可药物化的”，因为结合表面太大且无特征而不能被符合标准的5规则的小分子阻断。最近，已经尝试对口服生物可利用但超出五规则（bRo 5）的分子进行编目，以获得这些目标。 大环肽可以占据这种bRo 5空间，使用肽作为bRo 5分子的一个关键优势是，有许多成熟的技术可以从大量的文库中找到肽结合剂。 可以说，这些技术中最强大的是mRNA展示，它允许创建包含超过10万亿个变体的肽库，比在珠上制备的标准肽库大6-7个数量级。这些文库的极端多样性使得抑制剂开发取得了许多成功。 然而，这些成功与真实的药物发现是脱节的，因为发现的肽太大而不符合bRo 5。 序列短且符合bRo 5的文库可以通过mRNA展示来创建，但这些文库缺乏发现有效抑制剂所需的多样性，因为标准mRNA展示受到遗传密码的限制，每个位置只有约20个变体。 在本提案中，将寻求加强这种职位多样性的战略。 这将首先涉及通过分离完全修饰的tRNA异源受体来打破标准遗传密码的简并性。 基于密码子阅读规则，预测这将允许向密码中添加10个非规范氨基酸（ncAA）。第二个目标集中于结合这些新定义的密码子阅读规则和先前描述的具有非天然碱基对的tRNA，以允许将遗传密码扩展到在每个位置使用40个单体。 该目标还将专注于开发和测试一组精心策划的氨酰-tRNA，以用于未来创建包含数十亿种变体的bRo 5兼容文库，用于药物发现。