Univ. Grenoble Alpes, CNRS, DCM UMR 5250, F-38000 Grenoble, France.
Chem Soc Rev. 2022 Oct 17;51(20):8756-8783. doi: 10.1039/d2cs00640e.
Click chemistry was extensively used to decorate synthetic multivalent scaffolds with glycans to mimic the cell surface glycocalyx and to develop applications in glycosciences. Conjugation methods such as oxime ligation, copper(I)-catalyzed alkyne-azide cycloaddition, thiol-ene coupling, squaramide coupling or Lansbury aspartylation proved particularly suitable to achieve this purpose. This review summarizes the synthetic strategies that can be used either in a stepwise manner or in an orthogonal one-pot approach, to conjugate multiple copies of identical or different glycans to cyclopeptide scaffolds (namely multivalent glycocyclopeptides) having different size, valency, geometry and molecular composition. The second part of this review will describe the potential of these structures to interact with various carbohydrate binding proteins or to stimulate immunity against tumor cells.
点击化学被广泛用于用聚糖修饰合成的多价支架,以模拟细胞表面糖萼,并在糖科学中开发应用。偶联方法,如肟连接、铜 (I) 催化的炔烃-叠氮环加成、硫醇-烯烃偶联、螺环酰胺偶联或 Lansbury 天冬氨酸酰化,被证明特别适合实现这一目的。这篇综述总结了可以分步或正交一锅法使用的合成策略,将相同或不同聚糖的多个拷贝连接到具有不同大小、价态、几何形状和分子组成的环肽支架(即多价糖环肽)上。这篇综述的第二部分将描述这些结构与各种碳水化合物结合蛋白相互作用或刺激针对肿瘤细胞的免疫的潜力。