Molecular and Structural Studies of Antibody Diversity Mechanisms
抗体多样性机制的分子和结构研究
基本信息
- 批准号:8930163
- 负责人:
- 金额:$ 36.01万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2014
- 资助国家:美国
- 起止时间:2014-09-30 至 2018-07-31
- 项目状态:已结题
- 来源:
- 关键词:AffinityAmino AcidsAntibodiesAntibody DiversityAntigensArchitectureBindingCattleColorCrystallographyDataDiagnosticDisulfidesEngineeringFlow CytometryGeneticHealthImmunoglobulin DomainImmunoglobulinsKnowledgeLeadLibrariesMammalsMedicalModelingMolecularMutagenesisPatternPeptidesPharmaceutical PreparationsPhylogenyProcessPropertyProtein EngineeringProteinsResearchRoleStructureSurface ImmunoglobulinsSystemTherapeuticVariantantibody engineeringantigen bindingdeep sequencingdisulfide bonddrug developmentnovelphysical propertyresearch studyscaffold
项目摘要
DESCRIPTION (provided by applicant): Antibody molecules are enormously important as therapeutic and diagnostic molecules. More recently, unique scaffolds like the VHH of camelids, or even non-antibody frameworks like "knottins" have become important in biomedicine. Antibody diversity and antigen binding in mammals is often restricted to the CDR loops of the immunoglobulin fold. In experiments challenging this paradigm, we have recently solved the crystal structures of two bovine antibodies containing ultralong CDR H3s (56 and 61 amino acids) and also deep sequenced the ultralong repertoire. Our data reveal that these CDR H3s form a very unusual architecture composed of a long �-strand "stalk" which supports a disulfide rich "knob" that protrudes far from the immunoglobulin surface. Interestingly, the two different antibodies contain different patterns of disulfides, which result in different knob structures. Dee sequencing reveals extensive diversity in the ultralong CDR H3s where a multitude of different disulfides could potentially form within the knob. Thus, the bovine antibody system can produce an unprecedented repertoire of mega CDR H3s that may result in an impressive diversity of minifolds containing combinations of somatically generated disulfides. Thus, antibody diversity is located in a new minifold supported by the immunoglobulin domain. We will perform structural, functional, and engineering studies to investigate the properties of this new antibody class, as well as to lead the way to developing this unique structure into therapeutics.
描述(由申请人提供):抗体分子作为治疗和诊断分子非常重要。最近,独特的支架如骆驼科动物的VHH,甚至非抗体框架如“结蛋白”在生物医学中变得重要。哺乳动物中的抗体多样性和抗原结合通常限于免疫球蛋白折叠的CDR环。在挑战这种范式的实验中,我们最近解决了两种含有超长CDR H3(56和61个氨基酸)的牛抗体的晶体结构,并对超长库进行了深度测序。我们的数据显示,这些CDR H3形成了一个非常不寻常的结构,由一个长的β链“茎”组成,该茎支持一个富含二硫键的“球”,该球从免疫球蛋白表面突出很远。有趣的是,两种不同的抗体含有不同的二硫化物模式,这导致不同的结结构。Dee测序揭示了超长CDR H3的广泛多样性,其中多种不同的二硫化物可能在旋钮内形成。因此,牛抗体系统可以产生前所未有的mega CDR H3库,其可以导致含有体细胞产生的二硫化物的组合的微折叠的令人印象深刻的多样性。因此,抗体多样性位于由免疫球蛋白结构域支持的新微折叠中。我们将进行结构,功能和工程研究,以研究这种新抗体的性质,并引领将这种独特的结构开发成治疗方法。
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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PETER G SCHULTZ其他文献
PETER G SCHULTZ的其他文献
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{{ truncateString('PETER G SCHULTZ', 18)}}的其他基金
Synthesis at the Interface of Chemistry and Biology
化学与生物学交叉点的合成
- 批准号:
10596163 - 财政年份:2022
- 资助金额:
$ 36.01万 - 项目类别:
Synthesis at the Interface of Chemistry and Biology
化学与生物学交叉点的合成
- 批准号:
10406629 - 财政年份:2022
- 资助金额:
$ 36.01万 - 项目类别:
Experimentally Testing the Endosymbiotic Theory of Mitochondrial Evolution
实验检验线粒体进化的内共生理论
- 批准号:
9904721 - 财政年份:2019
- 资助金额:
$ 36.01万 - 项目类别:
An Orally Bioavailable Drug Candidate for Spinal Muscular Atrophy
一种治疗脊髓性肌萎缩症的口服生物利用候选药物
- 批准号:
9005317 - 财政年份:2016
- 资助金额:
$ 36.01万 - 项目类别:
Molecular and Structural Studies of Antibody Diversity Mechanisms
抗体多样性机制的分子和结构研究
- 批准号:
8631926 - 财政年份:2014
- 资助金额:
$ 36.01万 - 项目类别:
Ribosomal Synthesis of Peptides with Unnatural Building Blocks
具有非天然结构单元的肽的核糖体合成
- 批准号:
8082393 - 财政年份:2011
- 资助金额:
$ 36.01万 - 项目类别:
Ribosomal Synthesis of Peptides with Unnatural Building Blocks
具有非天然结构单元的肽的核糖体合成
- 批准号:
8412755 - 财政年份:2011
- 资助金额:
$ 36.01万 - 项目类别:
Ribosomal Synthesis of Peptides with Unnatural Building Blocks
具有非天然结构单元的肽的核糖体合成
- 批准号:
8268133 - 财政年份:2011
- 资助金额:
$ 36.01万 - 项目类别:
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