PENAMBATAN MOLEKUL GLUTATION FAUNA LAUT TERHADAP RESEPTOR DARI BEBERAPA PENYAKIT VIRUS

Q. X. A. Kai, I. Rumengan, Rosita A J Lintang, Stenly Wullur, Deiske A. Sumilat, Henneke Pangkey, Hein A Luntungan
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Abstract

Glutathion is a tripeptides produced by almost all living creatures, including marine fauna such as rotifers and shrimps. Judging from the important molecular role of glutathion in living cell,  the ability of glutathion as antiviral compound, has been assed by application of the AutodockTools to predict the ability of glutathion as ligand to bind receptors of several viral diseases such as  covid-19, malaria, and hepatitis B. Docking results of glutathion toward target receptor were shown by the parameter, Gibbs energy value, and supported by other data such as the amount of hidrogen bond, amino acid residues, and bond distance. Evidently, the glutathion could bind to  each receptor of covid-19, malaria and hepatitis B, with values of  Gibbs energy (∆G), -7,9, 7,1 and -7,1 kcal/mol, respectively. This proves that glutathion has ability to bind covid-19 receptor, even stronger than its ability to bind receptors of other viral diseases, and to the remdesevir. Between glutathion and covid-19 receptor, there were 11 hidrogen bonds, with distance ranged from 2,76 to 3,25 Å. These were stronger than those between glutathion and receptors of malaria and hepatitis B, only  8 and 4 Å hidrogen bonds, respectively.  To develop glutathion as antiviral drug, it is necessary to carry out in vitro and in vivo analyses, prior to clinical test. Therefore, it requires to explore the marine fauna species that produce glutathion and their cultivation.Keywords: molecular docking, glutathion, marine fauna, autodock vina, viral diseases, binding affinity
谷胱甘肽是一种三肽,几乎所有生物都能产生,包括轮虫和虾等海洋动物。鉴于谷胱甘肽在活细胞中的重要分子作用,应用AutodockTools对谷胱甘肽作为抗病毒化合物的能力进行了验证,预测了谷胱甘肽作为配体与几种病毒性疾病(如covid-19、疟疾、乙型肝炎)受体的结合能力。还有键长。显然,谷胱甘肽能与covid-19、疟疾和乙型肝炎的受体结合,其吉布斯能(∆G)值分别为-7、9、7、1和-7、1 kcal/mol。这证明谷胱甘肽具有结合covid-19受体的能力,甚至比其结合其他病毒性疾病受体的能力更强,并与瑞德西韦结合。谷胱甘肽与新冠病毒受体之间存在11个氢键,距离为2,76 ~ 3,25 Å。这些比谷胱甘肽与疟疾和乙型肝炎受体之间的更强,分别只有8个和4个Å氢键。为了开发谷胱甘肽作为抗病毒药物,有必要在临床试验之前进行体外和体内分析。因此,需要对生产谷胱甘肽的海洋动物种类及其养殖进行探索。关键词:分子对接;谷胱甘肽;海洋动物
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