William De Martini, Roksana Rahman, Eduvie Ojegba, Emily Jungwirth, Jasmine Macias, Frederick Ackerly, Mia Fowler, Jessica Cottrell, Tinchun Chu, Sulie L Chang
{"title":"激酶:了解它们在 HIV 感染中的作用。","authors":"William De Martini, Roksana Rahman, Eduvie Ojegba, Emily Jungwirth, Jasmine Macias, Frederick Ackerly, Mia Fowler, Jessica Cottrell, Tinchun Chu, Sulie L Chang","doi":"10.4236/wja.2019.93011","DOIUrl":null,"url":null,"abstract":"<p><p>Antiviral drugs currently on the market primarily target proteins encoded by specific viruses. The drawback of these drugs is that they lack antiviral mechanisms that account for resistance or viral mutation. Thus, there is a pressing need for researchers to explore and investigate new therapeutic agents with other antiviral strategies. Viruses such as the human immunodeficiency virus (HIV) alter canonical signaling pathways to create a favorable biochemical environment for infectivity. We used Qiagen Ingenuity Pathway Analysis (IPA) software to review the function of several cellular kinases and the resulting perturbed signaling pathways during HIV infection such as NF-κB signaling. These host cellular kinases such as ADK, PKR, MAP3K11 are involved during HIV infection at various stages of the life cycle. Additionally IPA analysis indicated that these modified host cellular kinases are known to have interactions with each other especially AKT1, a serine/threonine kinase involved in multiple pathways. We present a list of cellular host kinases and other proteins that interact with these kinases. This approach to understanding the relationship between HIV infection and kinase activity may introduce new drug targets to arrest HIV infectivity.</p>","PeriodicalId":23815,"journal":{"name":"World Journal of AIDS","volume":"9 3","pages":"142-160"},"PeriodicalIF":0.0000,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118713/pdf/","citationCount":"0","resultStr":"{\"title\":\"Kinases: Understanding Their Role in HIV Infection.\",\"authors\":\"William De Martini, Roksana Rahman, Eduvie Ojegba, Emily Jungwirth, Jasmine Macias, Frederick Ackerly, Mia Fowler, Jessica Cottrell, Tinchun Chu, Sulie L Chang\",\"doi\":\"10.4236/wja.2019.93011\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Antiviral drugs currently on the market primarily target proteins encoded by specific viruses. The drawback of these drugs is that they lack antiviral mechanisms that account for resistance or viral mutation. Thus, there is a pressing need for researchers to explore and investigate new therapeutic agents with other antiviral strategies. Viruses such as the human immunodeficiency virus (HIV) alter canonical signaling pathways to create a favorable biochemical environment for infectivity. We used Qiagen Ingenuity Pathway Analysis (IPA) software to review the function of several cellular kinases and the resulting perturbed signaling pathways during HIV infection such as NF-κB signaling. These host cellular kinases such as ADK, PKR, MAP3K11 are involved during HIV infection at various stages of the life cycle. Additionally IPA analysis indicated that these modified host cellular kinases are known to have interactions with each other especially AKT1, a serine/threonine kinase involved in multiple pathways. We present a list of cellular host kinases and other proteins that interact with these kinases. This approach to understanding the relationship between HIV infection and kinase activity may introduce new drug targets to arrest HIV infectivity.</p>\",\"PeriodicalId\":23815,\"journal\":{\"name\":\"World Journal of AIDS\",\"volume\":\"9 3\",\"pages\":\"142-160\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2019-09-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7118713/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"World Journal of AIDS\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4236/wja.2019.93011\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2019/9/9 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"World Journal of AIDS","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/wja.2019.93011","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2019/9/9 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目前市场上的抗病毒药物主要针对特定病毒编码的蛋白质。这些药物的缺点是缺乏抗病毒机制,无法解决抗药性或病毒变异问题。因此,研究人员迫切需要探索和研究具有其他抗病毒策略的新治疗药物。人类免疫缺陷病毒(HIV)等病毒会改变典型的信号通路,为感染性创造有利的生化环境。我们使用 Qiagen Ingenuity Pathway Analysis (IPA) 软件研究了几种细胞激酶的功能以及在 HIV 感染过程中由此产生的信号通路(如 NF-κB 信号传导)。这些宿主细胞激酶(如 ADK、PKR、MAP3K11)参与了 HIV 感染过程中生命周期的各个阶段。此外,IPA 分析表明,这些经过修饰的宿主细胞激酶之间存在相互作用,尤其是 AKT1,它是一种参与多种途径的丝氨酸/苏氨酸激酶。我们列出了细胞宿主激酶以及与这些激酶相互作用的其他蛋白质。这种了解艾滋病病毒感染与激酶活性之间关系的方法可能会为抑制艾滋病病毒感染带来新的药物靶点。
Kinases: Understanding Their Role in HIV Infection.
Antiviral drugs currently on the market primarily target proteins encoded by specific viruses. The drawback of these drugs is that they lack antiviral mechanisms that account for resistance or viral mutation. Thus, there is a pressing need for researchers to explore and investigate new therapeutic agents with other antiviral strategies. Viruses such as the human immunodeficiency virus (HIV) alter canonical signaling pathways to create a favorable biochemical environment for infectivity. We used Qiagen Ingenuity Pathway Analysis (IPA) software to review the function of several cellular kinases and the resulting perturbed signaling pathways during HIV infection such as NF-κB signaling. These host cellular kinases such as ADK, PKR, MAP3K11 are involved during HIV infection at various stages of the life cycle. Additionally IPA analysis indicated that these modified host cellular kinases are known to have interactions with each other especially AKT1, a serine/threonine kinase involved in multiple pathways. We present a list of cellular host kinases and other proteins that interact with these kinases. This approach to understanding the relationship between HIV infection and kinase activity may introduce new drug targets to arrest HIV infectivity.