• 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

塑造 SARS-CoV-2 刺突糖蛋白对人类受体 ACE2 适应性的协同进化力量。

Coevolutionary forces shaping the fitness of SARS-CoV-2 spike glycoprotein against human receptor ACE2.

机构信息

Department of Botany, Purnea Mahila College, Purnia, Bihar, India.

Department of Bioinformatics, Central University of South Bihar, Gaya, Bihar, India.

出版信息

Infect Genet Evol. 2021 Jan;87:104646. doi: 10.1016/j.meegid.2020.104646. Epub 2020 Nov 27.

DOI:10.1016/j.meegid.2020.104646
PMID:33249264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7691136/
Abstract

The current global health problem caused by SARS-CoV-2 has challenged the scientific community in various ways. Therefore, worldwide several scientific groups are exploring SARS-CoV-2 from different aspects including its origin, spread, severe infectivity, and also to find a cure. It is now well known that spike glycoprotein helps SARS-CoV-2 to enter inside the human host through a cellular receptor ACE2. However, the role of coevolutionary forces that makes SARS-CoV-2 spike glycoprotein more fit towards its human host remains unexplored. Therefore, in present bioinformatics study we identify coevolving amino acids in spike glycoprotein. Additionally, the effects of coevolution on the stability of the spike glycoprotein as well as its binding with receptor ACE2 were predicted. The results clearly indicate that coevolutionary forces play a pivotal role in increasing the fitness of spike glycoprotein against ACE2.

摘要

当前由 SARS-CoV-2 引起的全球健康问题以各种方式挑战着科学界。因此,全球有几个科学小组从其起源、传播、严重传染性等方面探索 SARS-CoV-2,也在寻找治疗方法。现在人们已经清楚,刺突糖蛋白帮助 SARS-CoV-2 通过细胞受体 ACE2 进入人体宿主。然而,使 SARS-CoV-2 刺突糖蛋白更适应人类宿主的协同进化力量的作用仍未得到探索。因此,在目前的生物信息学研究中,我们确定了刺突糖蛋白中的共进化氨基酸。此外,还预测了共进化对刺突糖蛋白稳定性及其与受体 ACE2 结合的影响。结果清楚地表明,协同进化力量在提高刺突糖蛋白对 ACE2 的适应性方面起着关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/209a3ee4fc75/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/9e8d9dd35465/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/7fb155949992/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/37427a6ad875/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/6f33b98b8093/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/209a3ee4fc75/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/9e8d9dd35465/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/7fb155949992/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/37427a6ad875/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/6f33b98b8093/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7eda/7691136/209a3ee4fc75/gr5_lrg.jpg

相似文献

1
Coevolutionary forces shaping the fitness of SARS-CoV-2 spike glycoprotein against human receptor ACE2.塑造 SARS-CoV-2 刺突糖蛋白对人类受体 ACE2 适应性的协同进化力量。
Infect Genet Evol. 2021 Jan;87:104646. doi: 10.1016/j.meegid.2020.104646. Epub 2020 Nov 27.
2
Coevolution, Dynamics and Allostery Conspire in Shaping Cooperative Binding and Signal Transmission of the SARS-CoV-2 Spike Protein with Human Angiotensin-Converting Enzyme 2.新冠病毒刺突蛋白与人血管紧张素转化酶 2 协同结合和信号转导的共进化、动力学和变构协同作用。
Int J Mol Sci. 2020 Nov 4;21(21):8268. doi: 10.3390/ijms21218268.
3
In silico studies on the comparative characterization of the interactions of SARS-CoV-2 spike glycoprotein with ACE-2 receptor homologs and human TLRs.基于 SARS-CoV-2 刺突糖蛋白与 ACE-2 受体同源物和人类 TLR 相互作用的比较特征的计算机研究。
J Med Virol. 2020 Oct;92(10):2105-2113. doi: 10.1002/jmv.25987. Epub 2020 May 17.
4
Angiotensin-Converting Enzyme 2 (ACE2) in the Pathogenesis of ARDS in COVID-19.血管紧张素转换酶 2(ACE2)在 COVID-19 所致急性呼吸窘迫综合征发病机制中的作用。
Front Immunol. 2021 Dec 22;12:732690. doi: 10.3389/fimmu.2021.732690. eCollection 2021.
5
Molecular dynamic simulation analysis of SARS-CoV-2 spike mutations and evaluation of ACE2 from pets and wild animals for infection risk.SARS-CoV-2 刺突突变的分子动力学模拟分析及宠物和野生动物 ACE2 感染风险评估。
Comput Biol Chem. 2022 Feb;96:107613. doi: 10.1016/j.compbiolchem.2021.107613. Epub 2021 Dec 1.
6
Optimized Pseudotyping Conditions for the SARS-COV-2 Spike Glycoprotein.SARS-COV-2 刺突糖蛋白的优化假型条件。
J Virol. 2020 Oct 14;94(21). doi: 10.1128/JVI.01062-20.
7
The expression of hACE2 receptor protein and its involvement in SARS-CoV-2 entry, pathogenesis, and its application as potential therapeutic target.hACE2 受体蛋白的表达及其在 SARS-CoV-2 进入、发病机制中的作用及其作为潜在治疗靶点的应用。
Tumour Biol. 2021;43(1):177-196. doi: 10.3233/TUB-200084.
8
SARS-CoV-2 Entry Receptor ACE2 Is Expressed on Very Small CD45 Precursors of Hematopoietic and Endothelial Cells and in Response to Virus Spike Protein Activates the Nlrp3 Inflammasome.SARS-CoV-2 进入受体 ACE2 表达于造血和内皮细胞的非常小的 CD45 前体上,并且响应病毒刺突蛋白激活 Nlrp3 炎性小体。
Stem Cell Rev Rep. 2021 Feb;17(1):266-277. doi: 10.1007/s12015-020-10010-z.
9
Site Density Functional Theory and Structural Bioinformatics Analysis of the SARS-CoV Spike Protein and hACE2 Complex.SARS-CoV 刺突蛋白与 hACE2 复合物的基于位点的密度泛函理论和结构生物信息学分析。
Molecules. 2022 Jan 26;27(3):799. doi: 10.3390/molecules27030799.
10
Q493K and Q498H substitutions in Spike promote adaptation of SARS-CoV-2 in mice.S 蛋白 493 位和 498 位的 Q 突变为 SARS-CoV-2 在小鼠体内的适应性进化提供了条件。
EBioMedicine. 2021 May;67:103381. doi: 10.1016/j.ebiom.2021.103381. Epub 2021 May 14.

引用本文的文献

1
Selection among site-dependent structurally constrained substitution models of protein evolution by approximate Bayesian computation.基于近似贝叶斯计算的蛋白质进化中依赖于位置的结构约束替代模型的选择。
Bioinformatics. 2024 Mar 4;40(3). doi: 10.1093/bioinformatics/btae096.
2
Motifs in SARS-CoV-2 evolution.SARS-CoV-2 进化中的基序。
RNA. 2023 Dec 18;30(1):1-15. doi: 10.1261/rna.079557.122.
3
Antiviral Drug Target Identification and Ligand Discovery.抗病毒药物靶点的鉴定和配体发现。
Methods Mol Biol. 2024;2714:85-99. doi: 10.1007/978-1-0716-3441-7_4.
4
Molecular Evolution of SARS-CoV-2 during the COVID-19 Pandemic.SARS-CoV-2 的分子进化与 COVID-19 大流行期间。
Genes (Basel). 2023 Feb 4;14(2):407. doi: 10.3390/genes14020407.
5
Severe Acute Respiratory Syndrome Type 2-Causing Coronavirus: Variants and Preventive Strategies.严重急性呼吸系统综合征 2 型冠状病毒:变异株与预防策略。
Adv Sci (Weinh). 2022 Apr;9(11):e2104495. doi: 10.1002/advs.202104495. Epub 2022 Jan 17.
6
Underlying selection for the diversity of spike protein sequences of SARS-CoV-2.SARS-CoV-2 刺突蛋白序列多样性的潜在选择。
IUBMB Life. 2022 Mar;74(3):213-220. doi: 10.1002/iub.2577. Epub 2021 Nov 25.
7
Genomic Variation and Diversification in Begomovirus Genome in Implication to Host and Vector Adaptation.双生病毒基因组的基因组变异与多样化及其对寄主和介体适应性的影响
Plants (Basel). 2021 Aug 19;10(8):1706. doi: 10.3390/plants10081706.
8
COVID-19: breaking down a global health crisis.COVID-19:破解一场全球健康危机。
Ann Clin Microbiol Antimicrob. 2021 May 18;20(1):35. doi: 10.1186/s12941-021-00438-7.
9
Clade GR and clade GH isolates of SARS-CoV-2 in Asia show highest amount of SNPs.亚洲的 SARS-CoV-2 的 clade GR 和 clade GH 分离株显示出最高数量的 SNPs。
Infect Genet Evol. 2021 Apr;89:104724. doi: 10.1016/j.meegid.2021.104724. Epub 2021 Jan 19.