Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
Department of Materials Science and Engineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Cancer Center at Illinois (CCIL), Urbana, IL 61801, USA; Department of Bioengineering, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Carle College of Medicine, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Materials Research Laboratory, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA; Institute for Genomic Biology, University of Illinois at Urbana-Champaign, Urbana, IL 61801, USA.
J Control Release. 2022 Jul;347:164-174. doi: 10.1016/j.jconrel.2022.05.007. Epub 2022 May 11.
Metabolic glycan labeling provides a facile yet powerful tool to install chemical tags to the cell membrane via metabolic glycoengineering processes of unnatural sugars. These cell-surface chemical tags can then mediate targeted conjugation of therapeutic agents via efficient chemistries, which has been extensively explored for cancer-targeted treatment. However, the commonly used in vivo chemistries such as azide-cyclooctyne and tetrazine-cyclooctene chemistries only allow for one-time use of cell-surface chemical tags, posing a challenge for long-term, continuous cell targeting. Here we show that cell-surface ketone groups can be recycled back to the cell membrane after covalent conjugation with hydrazide-bearing molecules, enabling repetitive targeting of hydrazide-bearing agents. Upon conjugation to ketone-labeled cancer cells via a pH-responsive hydrazone linkage, Alexa Fluor 488-hydrazide became internalized and entered endosomes/lysosomes where ketone-sugars can be released and recycled. The recycled ketone groups could then mediate targeted conjugation of Alexa Fluor 647-hydrazide. We also showed that doxorubicin-hydrazide can be targeted to ketone-labeled cancer cells for enhanced cancer cell killing. This study validates the recyclability of cell-surface chemical tags for repetitive targeting of cancer cells with the use of a reversible chemistry, which will greatly facilitate future development of potent cancer-targeted therapies based on metabolic glycan labeling.
代谢糖基化标记为通过非天然糖的代谢糖基工程过程将化学标签安装到细胞膜上提供了一种简便而强大的工具。然后,这些细胞表面化学标签可以通过有效的化学方法介导治疗剂的靶向缀合,这在癌症靶向治疗中得到了广泛的探索。然而,常用的体内化学方法,如叠氮环辛炔和四嗪环辛烯化学方法,仅允许细胞表面化学标签一次性使用,这对长期、连续的细胞靶向提出了挑战。在这里,我们表明,在与含有酰肼的分子发生共价缀合后,细胞表面的酮基团可以回收回细胞膜,从而实现对含有酰肼的试剂的重复靶向。通过 pH 响应腙键将 Alexa Fluor 488-酰肼缀合到酮标记的癌细胞上,Alexa Fluor 488-酰肼被内化并进入内体/溶酶体,其中酮糖可以被释放和回收。然后,回收的酮基团可以介导 Alexa Fluor 647-酰肼的靶向缀合。我们还表明,阿霉素-酰肼可以靶向酮标记的癌细胞,以增强对癌细胞的杀伤作用。这项研究验证了细胞表面化学标签的可回收性,用于通过可逆化学方法对癌细胞进行重复靶向,这将极大地促进基于代谢糖基化标记的有效癌症靶向治疗的未来发展。