Coronil effectively inhibits the interaction of clinically relevant Omicron mutants of SARS-CoV-2 spike proteins with human ACE2 receptor

Q3 Pharmacology, Toxicology and Pharmaceutics
Acharya Balkrishna , Rishabh Dev , Sandeep Kumar , Anurag Varshney
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Abstract

Background

Accumulating evidence suggests that the receptor binding domain (RBD) of the SARS-CoV-2 Omicron variant has several times more binding affinity to the human angiotensin-converting enzyme 2 (ACE2) receptor compared to the RBD of the original Covid-19 strain. This increased binding affinity of the Omicron variant is responsible for its increased internalization and infectivity.

Purpose

In the present study, the impact of Coronil, a tri-herbal formulation of extracts from Withania somnifera, Tinospora cordifolia and Ocimum sanctum on the binding properties of Omicron SARS-CoV-2 variant spike proteins (S proteins) was investigated.

Methods

Chemical composition of Coronil was determined by the Prominence-XR UHPLC system. The ELISA-based ACE2 binding inhibition assay was performed to delineate the effect of Coronil on the interaction between human ACE2 receptor and different Omicron variant S-proteins such as BA.4/BA5, XBB, BA.2.75.2, BA4.6/BF.7, BA.2.75.2, BQ.1.1 and a recently found spike protein variant JN.1 which is thought to emerge from BA.2.86.

Results

Coronil showed a dose-dependent inhibitory effect on the interactions between ACE2 and receptor binding domains (RBD) of all variants of S-proteins evaluated in this study including the recently emerged, highly transmissible variant spike protein JN.1. Although, Coronil significantly reduced the binding percentage in almost all the variant spike proteins, the maximum inhibition was achieved against BA.4/BA.5 where it inhibited the S protein – ACE2 interaction even at a low concentration of 3 µg/ml (16.6 %). This binding inhibition was further increased to 60.3 and 84.3 % at 100 and 300 µg/ml respectively.

Conclusion

This capability of Coronil to inhibit the binding of S-protein variants with ACE2 receptor may interfere with viral binding and internalization resulting in reduced infectivity of these Omicron spike protein variants. Overall, our data underscores the potential of Coronil in combating the various newly emerged Omicron spike protein variants. These findings may provide a basis for further studies of Coronil for its clinical effectiveness against these Omicron variants.

Abstract Image

Coronil有效抑制SARS-CoV-2刺突蛋白临床相关组粒突变体与人ACE2受体的相互作用
越来越多的证据表明,SARS-CoV-2 Omicron变体的受体结合域(RBD)与人血管紧张素转换酶2 (ACE2)受体的结合亲和力比原始Covid-19菌株的RBD高数倍。这种增加的Omicron变体的结合亲和力是其增加的内化和传染性的原因。目的研究由苦荞麦、堇青花和牡荆三种植物提取物组成的复方Coronil对Omicron SARS-CoV-2变异刺突蛋白(S蛋白)结合特性的影响。方法采用日珥- xr高效液相色谱法测定其化学成分。以elisa为基础的ACE2结合抑制实验研究了Coronil对ACE2受体与不同的Omicron变体s蛋白(BA.4/BA5、XBB、BA.2.75.2、BA4.6/BF)相互作用的影响。7、BA.2.75.2、BQ.1.1和最近发现的刺突蛋白变体JN.1,该变体被认为来自BA.2.86。结果scoronil对所有s蛋白变体ACE2与受体结合域(RBD)的相互作用均有剂量依赖性抑制作用,包括最近出现的高传染性变异spike蛋白JN.1。虽然Coronil显著降低了几乎所有变异刺突蛋白的结合率,但对BA.4/BA的抑制作用最大。5,即使在低浓度3µg/ml(16.6%)时也能抑制S蛋白- ACE2的相互作用。在100µg/ml和300µg/ml时,这种结合抑制率分别提高到60.3%和84.3%。结论Coronil抑制s蛋白变体与ACE2受体结合的能力可能干扰了病毒的结合和内化,从而降低了这些Omicron刺突蛋白变体的感染性。总的来说,我们的数据强调了Coronil在对抗各种新出现的Omicron刺突蛋白变体方面的潜力。这些发现可能为进一步研究冠状病毒对这些基因变异的临床疗效提供基础。
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来源期刊
Phytomedicine Plus
Phytomedicine Plus Medicine-Complementary and Alternative Medicine
CiteScore
3.70
自引率
0.00%
发文量
178
审稿时长
81 days
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