Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay

We previously reported that cervicovaginal lavages (CVL) contain a factor that enhances the replication of human immunodefeciency virus (HIV) by increasing virus transcription in T cells and monocytoid cells. This factor was named the HIV-inducing factor (HIF). To determine the molecular mass of HIF...

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Main Authors: Farhad B. Hashemi, Gregory T. Spear, Lawrence Madsen, Juergen Mollenhauer
Format: Article
Language:English
Published: Taylor & Francis Group 2000-03-01
Series:BioTechniques
Online Access:https://www.future-science.com/doi/10.2144/00283st05
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author Farhad B. Hashemi
Gregory T. Spear
Lawrence Madsen
Juergen Mollenhauer
author_facet Farhad B. Hashemi
Gregory T. Spear
Lawrence Madsen
Juergen Mollenhauer
author_sort Farhad B. Hashemi
collection DOAJ
description We previously reported that cervicovaginal lavages (CVL) contain a factor that enhances the replication of human immunodefeciency virus (HIV) by increasing virus transcription in T cells and monocytoid cells. This factor was named the HIV-inducing factor (HIF). To determine the molecular mass of HIF, we adapted a blot technique that involves nonreducing SDS-PAGE of CVL samples and electrophoretic transfer onto nitrocellulose paper followed by incubation of paper slices with HIV-infected monocytoid U1 cells. The slices with HIF bioactivity were detected by increased HIV production and measured by an HIV core protein (p24) ELISA. We refer to this technique as the “BioBlot” assay. The BioBlot assay successfully detected bioactivity of HIF anchored onto nitrocellulose and determined that HIF has a molecular mass of about 14 kDa. Paper slices with HIF-negative CVL samples as well as nitrocellulose paper samples without CVL did not enhance HIV production. This finding suggested that SDS-PAGE and nitrocellulose binding do not functionally alter the bioactive domain(s) of HIF structure. In addition to the detection of HIF bioactivity anchored to nitrocellulose and HIF molecular mass determination, the BioBlot technique offers an alternative, rapid method for other applications. These include the study of receptor-ligand interactions of mucosal proteins, direct bioactivity testing and molecular mass determination of secretory substances.
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spelling doaj-art-b8f70fd9e9c342e2a23d90bd32ee5cda2025-08-20T02:25:54ZengTaylor & Francis GroupBioTechniques0736-62051940-98182000-03-0128347848610.2144/00283st05Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot BioassayFarhad B. Hashemi0Gregory T. Spear1Lawrence Madsen2Juergen Mollenhauer31Rush University, Chicago, IL, USA1Rush University, Chicago, IL, USA1Rush University, Chicago, IL, USA1Rush University, Chicago, IL, USAWe previously reported that cervicovaginal lavages (CVL) contain a factor that enhances the replication of human immunodefeciency virus (HIV) by increasing virus transcription in T cells and monocytoid cells. This factor was named the HIV-inducing factor (HIF). To determine the molecular mass of HIF, we adapted a blot technique that involves nonreducing SDS-PAGE of CVL samples and electrophoretic transfer onto nitrocellulose paper followed by incubation of paper slices with HIV-infected monocytoid U1 cells. The slices with HIF bioactivity were detected by increased HIV production and measured by an HIV core protein (p24) ELISA. We refer to this technique as the “BioBlot” assay. The BioBlot assay successfully detected bioactivity of HIF anchored onto nitrocellulose and determined that HIF has a molecular mass of about 14 kDa. Paper slices with HIF-negative CVL samples as well as nitrocellulose paper samples without CVL did not enhance HIV production. This finding suggested that SDS-PAGE and nitrocellulose binding do not functionally alter the bioactive domain(s) of HIF structure. In addition to the detection of HIF bioactivity anchored to nitrocellulose and HIF molecular mass determination, the BioBlot technique offers an alternative, rapid method for other applications. These include the study of receptor-ligand interactions of mucosal proteins, direct bioactivity testing and molecular mass determination of secretory substances.https://www.future-science.com/doi/10.2144/00283st05
spellingShingle Farhad B. Hashemi
Gregory T. Spear
Lawrence Madsen
Juergen Mollenhauer
Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
BioTechniques
title Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
title_full Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
title_fullStr Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
title_full_unstemmed Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
title_short Detection and Molecular Mass Determination of an HIV Replication-Enhancing Female Genital Tract Factor Using a Blot Bioassay
title_sort detection and molecular mass determination of an hiv replication enhancing female genital tract factor using a blot bioassay
url https://www.future-science.com/doi/10.2144/00283st05
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