Literature DB >> 20015032

Blocking nuclear import of pre-integration complex: an emerging anti-HIV-1 drug discovery paradigm.

Peng Zhan1, Xinyong Liu, Erik De Clercq.   

Abstract

Although recent progress in highly active antiretroviral therapy (HAART) has provided an effective way to treat AIDS patients, the emergence of drug-resistant HIV-1 strains and drug toxicity during long-term treatment of HIV-infected patients necessitate the search for new targets that can be used to develop novel antiviral agents. One such target is the nuclear import process of the HIV pre-integration complex (PIC). The ability of HIV-1 using host cell nuclear import machinery to translocate the viral PIC into the cell nucleus is the critical determinant in the replication of the virus in non-dividing cells, such as macrophages. Compounds inhibiting HIV-1 nuclear import may be attractive candidates for novel anti-HIV development. In this review, we will describe the mechanisms of HIV-1 PIC translocation into the nucleus and the structure-function of the viral and cellular factors involved in this process, as well as several classes of novel anti-HIV compounds which target the nuclear import of HIV-1 PIC and effectively block viral replication.

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Year:  2010        PMID: 20015032     DOI: 10.2174/092986710790416335

Source DB:  PubMed          Journal:  Curr Med Chem        ISSN: 0929-8673            Impact factor:   4.530


  3 in total

Review 1.  Strategies to inhibit viral protein nuclear import: HIV-1 as a target.

Authors:  Aviad Levin; Abraham Loyter; Michael Bukrinsky
Journal:  Biochim Biophys Acta       Date:  2010-08-16

Review 2.  Pharmacological inhibition of feline immunodeficiency virus (FIV).

Authors:  Hakimeh Mohammadi; Dorothee Bienzle
Journal:  Viruses       Date:  2012-04-27       Impact factor: 5.048

3.  Identifying chemicals with potential therapy of HIV based on protein-protein and protein-chemical interaction network.

Authors:  Bi-Qing Li; Bing Niu; Lei Chen; Ze-Jun Wei; Tao Huang; Min Jiang; Jing Lu; Ming-Yue Zheng; Xiang-Yin Kong; Yu-Dong Cai
Journal:  PLoS One       Date:  2013-06-06       Impact factor: 3.240

  3 in total

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