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Designed Auto-assembly of Nanostreptabodies for Rapid Tissue-specific Targeting in Vivo

机译:设计的纳米链自动体内快速组织特异性靶向纳米链抗体的自动组装。

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摘要

Molecular medicine can benefit greatly from antibodies that deliver therapeutic and imaging agents to select organs and diseased tissues. Yet the development of complex and defined composite nanostructures remains a challenge that requires both designed stoichiometric assembly and superior in vivo testing ability. Here, we generate nanostructures called nanostreptabodies by controlled sequential assembly of biotin-engineered antibody fragments on a streptavidin scaffold with a defined capacity for additional biotinylated payloads such as other antibodies to create bispecific antibodies as well as organic and non-organic moieties. When injected intravenously, these novel and stable nanostructures exhibit exquisite targeting with tissue-specific imaging and delivery, including rapid transendothelial transport that enhances tissue penetration. This “tinkertoy construction” strategy provides a very flexible and efficient way to link targeting vectors with reporter and/or effector agents, thereby providing virtually endless combinations potentially useful for multipurpose molecular and functional imaging in vivo as well as therapies.
机译:分子医学可以从抗体中受益匪浅,这些抗体可以将治疗剂和显像剂递送到特定器官和患病组织。然而,复杂且确定的复合纳米结构的开发仍然是一个挑战,既需要设计的化学计量装配,也需要出色的体内测试能力。在这里,我们通过控制链霉亲和素支架上生物素工程化抗体片段的顺序控制组装,产生了被称为纳米链抗体的纳米结构,链霉亲和素支架具有确定的能力,可用于其他生物素化的有效负载,例如其他抗体,以产生双特异性抗体以及有机和非有机部分。静脉注射时,这些新颖而稳定的纳米结构具有组织特异性成像和递送的精确靶向性,包括可增强组织穿透力的快速跨内皮运输。这种“基因组构建”策略提供了一种非常灵活而有效的方式,将靶向载体与报道分子和/或效应剂相连,从而提供了无穷无尽的组合,这些组合对于体内多用途分子和功能成像以及治疗很有用。

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