Molecular Probes for Biomembrane Recognition

用于生物膜识别的分子探针

• 批准号: 9353419
• 负责人: BRADLEY D. SMITH
• 金额: $ 37.67万
• 依托单位: UNIVERSITY OF NOTRE DAME
• 依托单位国家: 美国
• 财政年份: 1999
• 资助国家: 美国
• 起止时间: 1999-05-01 至 2020-07-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/9353419
• 关键词: Alpha Cell; Binding; Biodistribution; Biological Markers; Biological Preservation; Cell membrane; Cell surface; Cells; Cellular biology; Clinic; Clinical; Drug Kinetics; Endocytosis; Epithelial; Epithelial ovarian cancer; Event; Exhibits; Fluorescence; Fluorescent Probes; Goals; Histology; Image; Integrins; Libraries; Ligands; Light; Malignant Neoplasms; Malignant neoplasm of ovary; Mediating; Membrane; Methods; Microscopy; Molecular Probes; Molecular Target; Mus; Neoplasm Metastasis; Nerve; Nodule; Normal tissue morphology; Operative Surgical Procedures; Ovarian Carcinoma; Patient-Focused Outcomes; Patients; Peptides; Performance; Periodicity; Process; Property; Protocols documentation; Resected; Signal Transduction; Structure; Surface; Surgeon; System; Thinness; Time; Tissues; Translations; Tumor Debulking; base; bioimaging; cancer cell; cancer surgery; cell motility; cellular imaging; clinically relevant; combinatorial; design; experience; experimental study; fluorescence-guided surgery; improved; in vivo; innovation; member; migration; molecular imaging; mouse model; novel; pre-clinical; programs; receptor; scaffold; screening; single molecule; squaraine; survivorship; tumor; virtual

Project Summary/Abstract The objective is to produce new classes of near-infrared fluorescent, multivalent molecular probes for advanced cell microscopy studies of membrane receptor clustering and also for paradigm shifting applications in fluorescence guided surgery. There is evidence that multivalent probes bearing multiple copies of a receptor antagonist can trigger receptor clustering and cell endocytosis of the probe, which is highly desired for many imaging applications. But presently it is not possible to produce, by rational design, an effective multivalent molecular probe for reliable in vivo targeting. The first specific aim will utilize a new programmable pre- assembly method to rapidly produce libraries of intrinsically bright, photostable, near-infrared fluorescent molecular probes with systematically altered multivalent binding properties such as ligand loading, linker distance, and degree of PEGylation to control biodistribution. A 35-member library of multivalent probes will be prepared with each member bearing a different copy number of the cyclic pentapeptide, cRGDfK, a targeting ligand for integrin receptors. The fluorescent probes will target a broad range of cancers, but this proposal will focus on epithelial ovarian carcinoma, the most common clinical form of ovarian cancer. The probe library will be screened with ovarian cancer cells for ability to promote extensive integrin-mediated endocytosis. Cell microscopy experiments will use the best probes from the library to visualize and quantify multivalent clustering of integrin receptors, a centrally important but poorly defined process in cell biology events such as signaling, proliferation, migration, and cancer metastasis. The second specific aim will produce two different near-infrared fluorescent multivalent probes for use in fluorescence guided surgery. One sub-aim will produce an in vivo fluorescent probe that can image epithelial ovarian cancer in a clinically relevant mouse model. A novel imaging protocol will be developed to determine if an observed probe signal originates from a tumor nodule on the surface or buried deep in the tissue. The fluorescent probe will enable surgeons to identify tumor nodules that are <1 mm, which is more than ten times smaller than the nodule size currently removed during optimal cytoreductive surgery. Lowering the size of resected ovarian cancer nodules by an order of magnitude is predicted to increase patient survivorship after surgery. A second sub-aim will produce a high performance, fluorescent multivalent peptide probe that can help a surgeon to visualize thin and buried nerves and avoid damaging them. The high overall impact of the proposal derives from the innovation of the versatile pre- assembly synthesis method to rapidly prepare libraries of near-infrared fluorescent multivalent molecular probes for virtually any cell surface biomarker, and the significance of the two proposed fluorescent molecular probes for separate and clinically important applications in fluorescence guided surgery.

项目摘要/摘要 我们的目标是生产新型的近红外荧光多价分子探针，用于 膜受体聚集的高级细胞显微镜研究及其范式转换应用 在荧光引导手术中。有证据表明，携带多个受体副本的多价探针 拮抗剂可以触发探针的受体聚集和细胞内吞作用，这是许多人非常想要的 成像应用程序。但目前，通过合理的设计，不可能生产出有效的多价 用于可靠的体内靶向的分子探针。第一个具体目标将利用一种新的可编程预置 快速生产本征亮、光稳定、近红外荧光库的组装方法 具有系统改变的多价结合性质的分子探针，如配体负载、连接物 距离和聚乙二醇化程度，以控制生物分布。由35名成员组成的多价探针文库将是 用每个带有不同拷贝数的环状五肽cRGDfK的成员制备，靶向 整合素受体的配体。荧光探针将针对广泛的癌症，但这项提议将 重点关注卵巢上皮癌，卵巢癌最常见的临床形式。探针库将 用卵巢癌细胞筛选促进广泛的整合素介导的内吞作用的能力。细胞 显微镜实验将使用文库中最好的探针来可视化和量化多价聚集 整合素受体，在信号等细胞生物学事件中是一个核心重要但定义不清的过程， 增殖、迁移和癌症转移。第二个特定目标将产生两种不同的近红外 用于荧光引导手术的荧光多价探针。一个子目标将在体内产生 可以在临床相关的小鼠模型中对上皮性卵巢癌进行成像的荧光探针。一本小说 将开发成像方案，以确定观察到的探测信号是否来自于 组织表面或深埋在组织中。这种荧光探针将使外科医生能够识别肿瘤结节 1毫米，这比目前在最佳时间内切除的结节大小小十倍以上 细胞减少术。将切除的卵巢癌结节的大小降低一个数量级 预计将提高手术后患者的存活率。第二个子目标将产生高性能， 荧光多价多肽探针，可以帮助外科医生可视化细小和埋藏的神经，并避免 对他们造成伤害。该提案的高整体影响来自于多功能Pre-One的创新 一种快速制备近红外荧光多价分子文库的组装合成法 几乎任何细胞表面生物标记物的探针，以及提出的两个荧光分子的意义 在荧光引导手术中用于分离和临床重要应用的探头。