d'Orchymont Faustine, Holland Jason P
University of Zurich, Department of Chemistry, Winterthurerstrasse 190, 8057, Zurich, Switzerland.
Angew Chem Int Ed Engl. 2022 Jul 18;61(29):e202204072. doi: 10.1002/anie.202204072. Epub 2022 May 20.
Mechanically interlocked molecules present opportunities to construct therapeutic drugs and diagnostic imaging agents but harnessing supramolecular chemistry to make biologically active probes in water is a challenge. Here, we describe a rotaxane-based approach to synthesise radiolabelled proteins and peptides for molecular imaging of cancer biomarkers in vivo. Host-guest chemistry using β-cyclodextrin- and cucurbit[6]uril-catalysed cooperative capture synthesis produced gallium-68 or zirconium-89 radiolabelled metallo[4]rotaxanes. Photochemical conjugation to trastuzumab led to a viable positron emission tomography (PET) radiotracer. The rotaxane architecture can be tuned to accommodate different radiometal ion complexes, other protein- or peptide-based drugs, and fluorophores for optical detection. This technology provides a platform to explore how mechanical bonding can improve drug delivery, enhance tumour specificity, control radiotracer pharmacokinetics, and reduce dosimetry.
机械互锁分子为构建治疗药物和诊断成像剂提供了机会,但利用超分子化学在水中制备具有生物活性的探针是一项挑战。在此,我们描述了一种基于轮烷的方法,用于合成放射性标记的蛋白质和肽,以在体内对癌症生物标志物进行分子成像。使用β-环糊精和葫芦[6]脲催化的主客体化学协同捕获合成产生了镓-68或锆-89放射性标记的金属[4]轮烷。与曲妥珠单抗进行光化学偶联产生了一种可行的正电子发射断层扫描(PET)放射性示踪剂。轮烷结构可以进行调整,以容纳不同的放射性金属离子络合物、其他基于蛋白质或肽的药物以及用于光学检测的荧光团。这项技术提供了一个平台,以探索机械键合如何改善药物递送、增强肿瘤特异性、控制放射性示踪剂的药代动力学并减少剂量测定。