Publication: Recombinant envelope protein of HIV-1 subtype E as antigen in HIV-1 antibody detection enzyme immunoassay
dc.contributor.author | Ruengpung Sutthent | en_US |
dc.contributor.author | Chinda Kanoksinsombat | en_US |
dc.contributor.author | Navin Horthongkham | en_US |
dc.contributor.author | Suda Louisirirotchanakul | en_US |
dc.contributor.author | Prasert Auewarakul | en_US |
dc.contributor.author | Wannee Kantakamalakul | en_US |
dc.contributor.other | Mahidol University | en_US |
dc.contributor.other | Faculty of Medicine, Siriraj Hospital, Mahidol University | en_US |
dc.date.accessioned | 2018-07-24T03:02:53Z | |
dc.date.available | 2018-07-24T03:02:53Z | |
dc.date.issued | 2002-12-01 | en_US |
dc.description.abstract | In order to develop a reliable and inexpensive serodiagnostic method to be used for anti-HIV antibody detection in Thailand, recombinant envelope (TM or gp41 subunit) protein of HIV-1 subtype E was produced from prokaryotic cell (Escherichia coli) as the source of antigen in enzyme immunoassay (TE diagnostic EIA kit). HIV-1 gp41 subunit of subtype E was successfully expressed in E. coli in the form of polyhistidine-tagged proteins, comprising of rgp41A (601 bases N-terminal half of TM or 25kDa) and rgp41B (560 bases C-terminal half of TM or 24 kDa) by using an expression vector, pBAD/His C. The amount of protein, dilution of sera, and anti-human IgG labeled HRP used in the EIA test optimized by a checker board titration of the protein and seropositive or seronegative sera, were 5.0 ng/ml, 1:300, and 1:4,000, respectively. The blinded test evaluation of TE-diagnostic EIA in 500 seropositive and 500 seronegative sera which have been simultaneously tested by two available commercial kits and compared with our TE diagnostic EIA, gave 99.6% sensitivity and specificity. The other known genetic subtypes sera such as subtype A (n=5), B (n=9), C (n=4) and D (n=5) were also positive with this EIA. The estimated manufacturer cost per test of rgp41 based anti-HIV antibody detection EIA or TE-diagnostic EIA was about 15 baht. This recombinant envelope (gp41 or TM) protein from HIV-1, which can be produced in large quantities without any hazards from growing the virus and has lower cost to produce anti-HIV antibody serological diagnostic kit, should be considered as an HIV screening test in Thailand. | en_US |
dc.identifier.citation | Southeast Asian Journal of Tropical Medicine and Public Health. Vol.33, No.2 (2002), 288-296 | en_US |
dc.identifier.issn | 01251562 | en_US |
dc.identifier.other | 2-s2.0-0036597939 | en_US |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/20268 | |
dc.rights | Mahidol University | en_US |
dc.rights.holder | SCOPUS | en_US |
dc.source.uri | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036597939&origin=inward | en_US |
dc.subject | Medicine | en_US |
dc.title | Recombinant envelope protein of HIV-1 subtype E as antigen in HIV-1 antibody detection enzyme immunoassay | en_US |
dc.type | Article | en_US |
dspace.entity.type | Publication | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=0036597939&origin=inward | en_US |