Krylova Natalya V, Kravchenko Anna O, Likhatskaya Galina N, Iunikhina Olga V, Glazunov Valery P, Zaporozhets Tatyana S, Shchelkanov Mikhail Y, Yermak Irina M
G.P. Somov Institute of Epidemiology and Microbiology, Rospotrebnadzor, 690087 Vladivostok, Russia.
G.B. Elyakov Pacific Institute of Bioorganic Chemistry, Far-Eastern Branch of the Russian Academy of Science, 690022 Vladivostok, Russia.
Int J Mol Sci. 2025 Jun 26;26(13):6175. doi: 10.3390/ijms26136175.
The diversity of structural types of carrageenans (CRGs)-sulfated polysaccharides of red algae-determines their different biological activities. The different types of CRGs (kappa, lambda, kappa/beta-CRGs) were isolated from the red algae of the Pacific coast. Molecular docking was performed to determine potential interactions of CRGs with the receptor-binding domain (RBD) of SARS-CoV-2 and its cellular receptor-angiotensin-converting enzyme type 2 (ACE2). CRGs interacted with ACE2 and RBD via hydrogen bonding and ionic interactions. The strongest binding affinity of CRGs and ACE2 was observed for kappa-CRG. Molecular docking was confirmed by results studying the effects of CRGs against SARS-CoV-2 in vitro. The ability of CRGs, as well as the complex CRG with sea urchin echinochrome (Ech), to inhibit SARS-CoV-2 replication in Vero E6 cells was studied using cytopathic effect (CPE) inhibition and RT-PCR assays. The simultaneous treatment of cells with CRGs and the virus revealed that kappa-CRG exhibited the most significant antiviral effect among all the polysaccharides, with a selective index (SI) of 33. The kappa-CRG/Ech complex exhibited the highest virucidal effect on SARS-CoV-2 particles with an SI above 70 (more than two times higher than that of CRG and Ech) and reduced viral RNA levels by 45% (IC = 45%). Our results illustrate that CRGs and kappa-CRG/Ech complex can act as protective agents against SARS-CoV-2.
角叉菜胶(CRGs)——红藻的硫酸化多糖——结构类型的多样性决定了它们不同的生物活性。从太平洋沿岸的红藻中分离出不同类型的CRGs(κ型、λ型、κ/β型CRGs)。进行分子对接以确定CRGs与严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的受体结合域(RBD)及其细胞受体——2型血管紧张素转换酶(ACE2)之间的潜在相互作用。CRGs通过氢键和离子相互作用与ACE2和RBD相互作用。观察到κ型CRG与ACE2的结合亲和力最强。通过研究CRGs在体外对SARS-CoV-2的影响的结果证实了分子对接。使用细胞病变效应(CPE)抑制和逆转录-聚合酶链反应(RT-PCR)分析研究了CRGs以及CRG与海胆紫球藻色素(Ech)的复合物在Vero E6细胞中抑制SARS-CoV-2复制的能力。用CRGs和病毒同时处理细胞表明,κ型CRG在所有多糖中表现出最显著的抗病毒作用,选择性指数(SI)为33。κ型CRG/Ech复合物对SARS-CoV-2颗粒表现出最高的杀病毒作用,SI高于70(比CRG和Ech高出两倍多),并使病毒RNA水平降低45%(IC = 45%)。我们的结果表明,CRGs和κ型CRG/Ech复合物可作为抗SARS-CoV-2的保护剂。