• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

采用基于 siRNA 的基因沉默方法抑制:一种计算方法。

Inhibition of Using siRNA-Based Gene Silencing Method: A Computational Approach.

机构信息

Department of Epidemiology and National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Agra, India.

Department of Immunology, National JALMA Institute for Leprosy and Other Mycobacterial Diseases, Agra, India.

出版信息

J Comput Biol. 2020 Jan;27(1):91-99. doi: 10.1089/cmb.2019.0156. Epub 2019 Aug 22.

DOI:10.1089/cmb.2019.0156
PMID:31433209
Abstract

Tuberculosis (TB) is a major public health problem in several countries. Development of first-line and second-line drug resistance strains of further complicated the management of the disease. Despite available drugs to treat TB, 1.6 million people died from the disease in 2017. In this study, we designed 10 siRNAs against 8 of and validated their usefulness for inhibition of protein synthesis by using computational approach. We found that the predicted siRNAs efficiently form seed duplex complex against their respective mRNA targets. Other different computational approaches were also undertaken to assess the stability, accessibility, and strength of seed duplex complex of designed siRNA and targeted mRNA. On the basis of the computational approach, we reciprocated that the technique will help in opening a new window in the field of TB control program and could be taken for further clinical studies to find their appropriateness for TB eradication.

摘要

结核病(TB)是多个国家的一个主要公共卫生问题。一线和二线耐药菌株的出现进一步使疾病的管理复杂化。尽管有治疗结核病的药物,但 2017 年仍有 160 万人死于该病。在这项研究中,我们设计了针对 8 个 的 10 个 siRNA,并通过计算方法验证了它们在抑制蛋白质合成方面的有用性。我们发现,预测的 siRNA 能够有效地针对各自的 mRNA 靶标形成种子双链复合物。还采用了其他不同的计算方法来评估设计的 siRNA 和靶向 mRNA 的种子双链复合物的稳定性、可及性和强度。基于计算方法,我们推测该技术将有助于在结核病控制项目领域开辟一个新窗口,并可进一步进行临床研究,以确定其在消除结核病方面的适宜性。

相似文献

1
Inhibition of Using siRNA-Based Gene Silencing Method: A Computational Approach.采用基于 siRNA 的基因沉默方法抑制:一种计算方法。
J Comput Biol. 2020 Jan;27(1):91-99. doi: 10.1089/cmb.2019.0156. Epub 2019 Aug 22.
2
A consequence of drug targeting of aminoacyl-tRNA synthetases in Mycobacteriumtuberculosis.结核分枝杆菌中氨酰-tRNA 合成酶的药物靶向的后果。
Chem Biol Drug Des. 2021 Sep;98(3):421-434. doi: 10.1111/cbdd.13865. Epub 2021 Jul 3.
3
[Development of antituberculous drugs: current status and future prospects].[抗结核药物的研发:现状与未来前景]
Kekkaku. 2006 Dec;81(12):753-74.
4
Toward the virtual screening of potential drugs in the homology modeled NAD+ dependent DNA ligase from Mycobacterium tuberculosis.迈向结核分枝杆菌同源建模的NAD+依赖性DNA连接酶潜在药物的虚拟筛选。
Protein Pept Lett. 2010 Feb;17(2):269-76. doi: 10.2174/092986610790225950.
5
Discovery of Novel Oral Protein Synthesis Inhibitors of Mycobacterium tuberculosis That Target Leucyl-tRNA Synthetase.发现靶向亮氨酰 - tRNA合成酶的新型结核分枝杆菌口服蛋白质合成抑制剂。
Antimicrob Agents Chemother. 2016 Sep 23;60(10):6271-80. doi: 10.1128/AAC.01339-16. Print 2016 Oct.
6
Susceptibility and mode of binding of the Mycobacterium tuberculosis cysteinyl transferase mycothiol ligase to tRNA synthetase inhibitors.结核分枝杆菌半胱氨酰转移酶 mycothiol 连接酶对 tRNA 合成酶抑制剂的敏感性和结合模式。
Bioorg Med Chem Lett. 2011 Apr 15;21(8):2480-3. doi: 10.1016/j.bmcl.2011.02.042. Epub 2011 Feb 17.
7
Drug resistance in Mycobacterium tuberculosis and targeting the l,d-transpeptidase enzyme.结核分枝杆菌的耐药性与 l,d-转肽酶的靶向作用。
Drug Dev Res. 2019 Feb;80(1):11-18. doi: 10.1002/ddr.21455. Epub 2018 Oct 12.
8
Identification of gene targets against dormant phase Mycobacterium tuberculosis infections.针对结核分枝杆菌潜伏感染的基因靶点鉴定。
BMC Infect Dis. 2007 Jul 26;7:84. doi: 10.1186/1471-2334-7-84.
9
Antibiotic Treatment Shapes the Antigenic Environment During Chronic TB Infection, Offering Novel Targets for Therapeutic Vaccination.抗生素治疗在慢性结核感染期间塑造抗原环境,为治疗性疫苗接种提供新的靶标。
Front Immunol. 2020 Apr 28;11:680. doi: 10.3389/fimmu.2020.00680. eCollection 2020.
10
Hairpin extensions enhance the efficacy of mycolyl transferase-specific antisense oligonucleotides targeting Mycobacterium tuberculosis.发夹式延伸增强了靶向结核分枝杆菌的分枝菌酸转移酶特异性反义寡核苷酸的功效。
Proc Natl Acad Sci U S A. 2007 Apr 24;104(17):7199-204. doi: 10.1073/pnas.0701725104. Epub 2007 Apr 16.

引用本文的文献

1
A Comprehensive Computational Investigation into the Conserved Virulent Proteins of species Unveils Potential Small-Interfering RNA Candidates as a New Therapeutic Strategy against Shigellosis.全面的计算研究揭示了 种保守的毒力蛋白,为志贺氏菌病的治疗提供了新的潜在小干扰 RNA 候选药物。
Molecules. 2022 Mar 17;27(6):1936. doi: 10.3390/molecules27061936.