Chamata Yara, Jackson Kim G, Watson Kimberly A, Jauregi Paula
Harry Nursten Building, Department of Food and Nutritional Sciences, University of Reading, Reading RG6 6DZ, UK.
Health and Life Sciences Building, School of Biological Sciences, University of Reading, Reading RG6 6EX, UK.
Int J Mol Sci. 2021 Oct 28;22(21):11662. doi: 10.3390/ijms222111662.
The renin-angiotensin system (RAS) is a key regulator of blood pressure and hypertension. Angiotensin-converting enzyme 2 (ACE2) and angiotensin-converting enzyme I (ACE) are two main components of the RAS that play a major role in blood pressure homeostasis. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) uses ACE2 as a receptor to enter cells. Despite some controversies, numerous studies have reported a significant association between the use of ACE inhibitors and reduced risk of COVID-19. In our previous studies, we produced and identified peptide sequences present in whey hydrolysates exhibiting high ACE inhibitory activity. Therefore, the aim of this work is to obtain an improved understanding of the function of these natural peptides as RAS inhibitors and investigate their potential therapeutic role in the COVID-19 pandemic. The molecular interactions between peptides IPP, LIVTQ, IIAE, LVYPFP, and human ACE2 were assessed by employing a molecular docking approach. The results show that natural whey-derived peptides have a dual inhibitory action against both ACE and ACE2. This dual activity distinguishes these ACE inhibitory peptides from synthetic drugs, such as Captopril and Lisinopril which were not shown to inhibit ACE2 activity, and may represent a potential strategy in the treatment of COVID-19.
肾素-血管紧张素系统(RAS)是血压和高血压的关键调节因子。血管紧张素转换酶2(ACE2)和血管紧张素转换酶I(ACE)是RAS的两个主要组成部分,在血压稳态中起主要作用。严重急性呼吸综合征冠状病毒2(SARS-CoV-2)利用ACE2作为受体进入细胞。尽管存在一些争议,但大量研究报告称使用血管紧张素转换酶抑制剂与降低2019冠状病毒病(COVID-19)风险之间存在显著关联。在我们之前的研究中,我们制备并鉴定了乳清水解物中具有高血管紧张素转换酶抑制活性的肽序列。因此,这项工作的目的是更好地了解这些天然肽作为RAS抑制剂的功能,并研究它们在COVID-19大流行中的潜在治疗作用。采用分子对接方法评估了肽IPP、LIVTQ、IIAE、LVYPFP与人ACE2之间的分子相互作用。结果表明,天然乳清来源的肽对ACE和ACE2均具有双重抑制作用。这种双重活性将这些血管紧张素转换酶抑制肽与合成药物(如未显示抑制ACE2活性的卡托普利和赖诺普利)区分开来,可能代表了治疗COVID-19的一种潜在策略。