Global Institute of Pharmaceutical Education and Research, Affiliated to Uttarakhand Technical University Kashipur- 244713, India.
Department of Pharmaceutics, Nirmala College of Pharmacy, Mangalagiri, Guntur, Affiliated to Acharya Nagarjuna University, Andhra Pradesh, 522503, India.
Curr Drug Targets. 2021;22(17):2006-2020. doi: 10.2174/1389450122666210309105820.
By the end of 2019, the sudden outbreak of the novel coronavirus disease (COVID-19) has become a global threat. It is called COVID-19 because it was caused by the novel coronavirus (SARS-COV-2) in 2019. A total of 1.9 M deaths and 87.9 M cases have been reported all over the world, where 49M cases have recovered so far. Scientists are working hard to find chemotherapeutics and vaccines for COVID-19. Mutations in SARS-CoV-2 have been observed in a combination of several hazardous stresses, making them more resistant and beneficial. So to break down the viral system, the disease targets are examined.
In today's review, a comprehensive study of spike protein explains the main purpose of the novel coronavirus and how to prevent the spread of the disease virus cross-transmission from infected to a healthy person.
Covid-19 has already been declared a pandemic by the World Health Organization (WHO) due to its result in causing death and severe illness globally. SARS-CoV-2 is highly contagious; however, the intermediate host of the novel coronavirus is not clear. To explore the mechanisms of disease, one of the viral targets, such as the spike protein that binds to human cells and causes the disease by altering its genetic structure which is considered along with potential inhibitors.
It has been shown that the interaction of receptor-binding domain (RBD) protein of SARS- CoV-2 spike and the angiotensin-converting enzyme 2 (ACE2) host receptor and further replication of coronavirus spike protein causes its invasion in the host cell. The human Lymphocyte antigen 6 complex, Locus E (LY6E), inhibits the entry of CoV into host cells by interfering with the human gene, inducing spike protein-mediated membrane fusion. Some natural formulations have also been shown to prevent spike protein from binding to the host cell.
With the development of the LY6E gene activator that can inhibit spike protein- ACE2-mediated membrane fusion, new opportunities for SARS-CoV-2 treatment may emerge. Existing antiviral fusion inhibitors and natural compounds targeting spike resistance can serve as a template for further SARS-CoV-2 drug formulation.
2019 年底,新型冠状病毒病(COVID-19)的突然爆发已成为全球性威胁。它之所以被称为 COVID-19,是因为它是由 2019 年新型冠状病毒(SARS-COV-2)引起的。全球已报告总共有 190 万人死亡,8790 万人感染,迄今为止已有 4900 万人康复。科学家们正在努力寻找针对 COVID-19 的化疗药物和疫苗。在多种危险压力的共同作用下,SARS-CoV-2 发生了突变,使它们更具抵抗力和益处。因此,为了破坏病毒系统,对疾病靶点进行了检查。
在今天的综述中,对刺突蛋白的综合研究解释了新型冠状病毒的主要目的,以及如何防止疾病病毒从感染者传播到健康人。
由于 COVID-19 在全球范围内导致死亡和严重疾病,世界卫生组织(WHO)已宣布其为大流行。SARS-CoV-2 具有高度传染性;然而,新型冠状病毒的中间宿主尚不清楚。为了探索疾病的机制,研究了病毒的一个靶点,例如刺突蛋白,它通过改变其遗传结构与潜在抑制剂一起结合到人类细胞上并引起疾病。
研究表明,SARS-CoV-2 刺突的受体结合域(RBD)蛋白与血管紧张素转换酶 2(ACE2)宿主受体的相互作用以及冠状病毒刺突蛋白的进一步复制导致其侵入宿主细胞。人类淋巴细胞抗原 6 复合物,位置 E(LY6E)通过干扰人类基因,诱导刺突蛋白介导的膜融合,抑制 CoV 进入宿主细胞。一些天然配方也已被证明可以防止刺突蛋白与宿主细胞结合。
随着可以抑制刺突蛋白- ACE2 介导的膜融合的 LY6E 基因激活剂的开发,可能会为 SARS-CoV-2 的治疗带来新的机会。针对刺突蛋白耐药性的现有抗病毒融合抑制剂和天然化合物可以作为进一步 SARS-CoV-2 药物制剂的模板。