Centro de Investigaciones en Química Biológica de Córdoba, CIQUIBIC, CONICET and Departamento de Química Biológica Ranwel Caputto, Facultad de Ciencias Químicas, Universidad Nacional de Córdoba, Ciudad Universitaria, Córdoba, Argentina.
Medicina Interna, Nuevo Hospital San Roque, Ministerio de Salud de la Provincia de Córdoba, Córdoba, Argentina.
J Biol Chem. 2021 Jan-Jun;296:100375. doi: 10.1016/j.jbc.2021.100375. Epub 2021 Feb 4.
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged during the last months of 2019, spreading throughout the world as a highly transmissible infectious illness designated as COVID-19. Vaccines have now appeared, but the challenges in producing sufficient material and distributing them around the world means that effective treatments to limit infection and improve recovery are still urgently needed. This review focuses on the relevance of different glycobiological molecules that could potentially serve as or inspire therapeutic tools during SARS-CoV-2 infection. As such, we highlight the glycobiology of the SARS-CoV-2 infection process, where glycans on viral proteins and on host glycosaminoglycans have critical roles in efficient infection. We also take notice of the glycan-binding proteins involved in the infective capacity of virus and in human defense. In addition, we critically evaluate the glycobiological contribution of candidate drugs for COVID-19 therapy such as glycans for vaccines, anti-glycan antibodies, recombinant lectins, lectin inhibitors, glycosidase inhibitors, polysaccharides, and numerous glycosides, emphasizing some opportunities to repurpose FDA-approved drugs. For the next-generation drugs suggested here, biotechnological engineering of new probes to block the SARS-CoV-2 infection might be based on the essential glycobiological insight on glycosyltransferases, glycans, glycan-binding proteins, and glycosidases related to this pathology.
严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)于 2019 年末出现,作为一种高传染性传染病迅速传播到世界各地,并被命名为 COVID-19。目前已经出现了疫苗,但在全球范围内生产足够数量的疫苗并进行分发仍面临挑战,因此仍然迫切需要有效的治疗方法来限制感染并促进康复。本综述重点介绍了不同糖生物学分子的相关性,这些分子在 SARS-CoV-2 感染过程中可能作为或启发治疗工具。因此,我们强调了 SARS-CoV-2 感染过程中的糖生物学,病毒蛋白上的聚糖和宿主糖胺聚糖在有效感染中起着关键作用。我们还注意到了参与病毒感染能力和人体防御的糖结合蛋白。此外,我们还批判性地评估了 COVID-19 治疗候选药物的糖生物学贡献,如疫苗用聚糖、抗聚糖抗体、重组凝集素、凝集素抑制剂、糖苷酶抑制剂、多糖和许多糖苷,强调了一些重新利用 FDA 批准药物的机会。对于这里建议的下一代药物,可以基于与该病理学相关的糖基转移酶、聚糖、糖结合蛋白和糖苷酶的基本糖生物学见解,通过生物技术工程来设计新的探针以阻断 SARS-CoV-2 的感染。