Beijing National Laboratory for Molecular Sciences, Key Laboratory of Bioorganic Chemistry and Molecular Engineering of Ministry of Education, College of Chemistry and Molecular Engineering, Synthetic and Functional Biomolecules Center, Peking-Tsinghua Center for Life Sciences, Peking University, Beijing 100871 (P.R. China).
Angew Chem Int Ed Engl. 2014 Dec 15;53(51):14082-6. doi: 10.1002/anie.201408442. Epub 2014 Oct 21.
Although it has been well known that dynamic changes in glycosylation are associated with tumor progression, it remains challenging to selectively visualize the cancer glycome in vivo. Herein, a strategy for the targeted imaging of tumor-associated glycans by using ligand-targeted liposomes encapsulating azidosugars is described. The intravenously injected liposomal nanoparticles selectively bound to the cancer-cell-specific receptors and installed azides into the melanoma glycans in a xenograft mouse model in a tissue-specific manner. Subsequently, a copper-free click reaction was performed in vivo to chemoselectively conjugate the azides with a near-infrared fluorescent dye. The glycosylation dynamics during tumor growth were monitored by in vivo fluorescence imaging. Furthermore, the newly synthesized sialylated glycoproteins were enriched during tumor growth and identified by glycoproteomics. Compared with the labeling methods using free azidosugars, this method offers improved labeling efficiency and high specificity and should facilitate the elucidation of the functional role of glycans in cancer biology.
尽管糖基化的动态变化与肿瘤进展有关已广为人知,但在体内选择性地可视化肿瘤糖组仍然具有挑战性。在此,描述了一种通过靶向含有叠氮化物的配体靶向脂质体来靶向成像肿瘤相关聚糖的策略。静脉内注射的脂质体纳米颗粒选择性地与癌细胞特异性受体结合,并以组织特异性的方式将叠氮化物安装到异种移植小鼠模型中的黑色素瘤糖上。随后,在体内进行无铜点击反应,以化学选择性地将叠氮化物与近红外荧光染料偶联。通过体内荧光成像监测肿瘤生长过程中的糖基化动态。此外,在肿瘤生长过程中还可以通过糖蛋白质组学富集新合成的唾液酸化糖蛋白并对其进行鉴定。与使用游离叠氮化物的标记方法相比,该方法提高了标记效率和特异性,应该有助于阐明糖在癌症生物学中的功能作用。