利用同源建模、分子动力学模拟和对接研究探索虹鳟促性腺激素受体的三维结构

Sheema Yaqoob Khan , Mohd Ashraf Rather , Azra Shah , Ishtiyaq Ahmad , Irfan Ahmad , KawKabul Saba , Faisal Rashid Sofi
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引用次数: 0

摘要

鱼类的生殖过程由下丘脑-垂体-性腺轴(HPG)调节,这一点与四足动物非常相似。在这一系统中,促性腺激素释放激素(GnRH)由下丘脑释放,与垂体中的 GnRH 受体结合,刺激促性腺激素激素的分泌。本研究旨在利用计算和结构生物学方法分析虹鳟鱼(Oncorhynchus mykiss)的 GnRH 受体。虹鳟的 GnRH 受体基因由 1707 个碱基对的核苷酸序列和 1251 个碱基对的开放阅读框组成,负责编码 416 个氨基酸。研究发现,GnRH 受体中含量最多的氨基酸是亮氨酸(L)。二级结构显示,α螺旋占最大比例(36%),有 153 个残基,其次是扩展链,有 77 个残基(17.51%)。GnRH 受体含有 26 个带负电荷的氨基酸残基和 37 个带正电荷的氨基酸残基。位于 310 位的赖氨酸(K)的亲水性最高,为-3.900,而位于 290 位的亮氨酸(L)的疏水性最高,为 3.80。分子对接分析表明,雌酮的结合能最高(-7.8 kcal/mol)。研究发现,雌孕酮能与 GnRH 的 MET160、LUE245、LUE62、TYR216 和 GLN209 残基形成氢键。此外,分子动力学研究表明,这些复合物形成了稳固而持久的连接,表明它们在整个模拟过程中结构完整。这项研究的结果为蛋白质建模、分子对接以及针对 GnRH 受体的拮抗配体的虚拟筛选提供了深入的见解。此外,这些结果可能会极大地帮助推进和改进针对各种鱼类生殖功能障碍的治疗策略。
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Exploring 3D structure of gonadotropin hormone receptor using homology modeling, molecular dynamic simulation and docking studies in rainbow trout, Oncorhynchus mykiss

Reproductive processes in fishes are regulated by the hypothalamic-pituitary-gonadal (HPG) axis, much like in tetrapods. Within this system, Gonadotropin-Releasing Hormone (GnRH) is released by the hypothalamus, binding to GnRH receptors in the pituitary gland and stimulating the secretion of gonadotropin hormones. The current study aimed to analyze the GnRH receptor in Oncorhynchus mykiss (rainbow trout) using a computational and structural biology approach. The GnRH receptor gene of O. mykiss comprises a nucleotide sequence of 1707 base pairs with an open reading frame of 1251 base pairs, which is responsible for encoding 416 amino acids. It was found that the GnRH receptor contains leucine (L) as the most abundant amino acid. The secondary structure revealed that alpha helices constitute the largest percentage (36 %) with 153 residues, followed by extended strands with 77 residues (17.51 %). The GnRH receptor contains 26 negatively charged and 37 positively charged amino acid residues. The highest hydrophilicity was observed for lysine (K) at position 310, with a value of −3.900, while the highest hydrophobicity was found for leucine (L) at position 290, with a value of 3.80. Molecular docking analysis showed that the most favorable binding energy was observed for Gestrinone (−7.8 kcal/mol). Gestrinone was found to form hydrogen bonds with MET160, LUE245, LUE62, TYR216, and GLN209 residues of GnRH. Moreover, molecular dynamics revealed that the complexes form robust and enduring connections, indicating their structural integrity throughout the simulation. The results of this study provide insights into the protein modeling, molecular docking, and virtual screening of antagonist ligands against the GnRH receptor. Additionally, they may significantly aid in the advancement and improvement of therapeutic strategies targeted at treating various fish reproductive dysfunctions.

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来源期刊
Endocrine and Metabolic Science
Endocrine and Metabolic Science Medicine-Endocrinology, Diabetes and Metabolism
CiteScore
2.80
自引率
0.00%
发文量
4
审稿时长
84 days
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