Insight into molecular and mutational scrutiny of epilepsy associated gene Gabrg2 leading to novel computer-aided drug designing

对癫痫相关基因Gabrg2的分子和突变研究的深入分析,为新型计算机辅助药物设计提供了可能。

阅读:2

Abstract

Epilepsy is a neurological disorder that is major cause of disability in the world. This is most severe medical condition related with different ion channel genes, inflammatory molecules depression and stress. For this purpose, precise diagnostic techniques are available. Genetic polymorphisms are major factors behind the occurrence of many disorders therefore they can be valid for diagnostic purpose. This study emphasis the finding of such markers in Lahore population. Epilepsy-causing gene GABRG2 was selected, and the gene was then examined to detect the presence of polymorphic markers with the help of molecular (PCR) and computational analysis. 50 blood samples of epilepsy patients were collected from Children hospital Lahore, out of which 2 samples were shown positive response for GABRG2 gene, indicating that this gene is becoming the cause of seizures in epilepsy patients. These samples underwent mutational screening, which revealed 6 new mutations in exon 3 region of these samples as a result of disease occurrence. There are no proper treatments of epilepsy offered despite the development of anti-leptic and anti-seizure drugs. To solve this issue, researchers are working to create innovative methods of treating epilepsy, that incorporate the use of herbal remedies. 31 plant compounds have been used in this study but only one compound cyanidin was selected on the base of best binding affinity. Moreover, SwissAdme, QSAR analysis and molecular simulations demonstrated that cyanidin is a best natural drug model which have best responses as compared to other epileptic drugs and can be tested for future application in laboratories.

特别声明

1、本页面内容包含部分的内容是基于公开信息的合理引用;引用内容仅为补充信息,不代表本站立场。

2、若认为本页面引用内容涉及侵权,请及时与本站联系,我们将第一时间处理。

3、其他媒体/个人如需使用本页面原创内容,需注明“来源:[生知库]”并获得授权;使用引用内容的,需自行联系原作者获得许可。

4、投稿及合作请联系:info@biocloudy.com。