Title of article :
Detection of Human Immunodeficiency Virus Type 1 Reverse Transcriptase Using Aptamers as Probes in Affinity Capillary Electrophoresis
Author/Authors :
Le، X. Chris نويسنده , , Pavski، Victor نويسنده ,
Issue Information :
دوهفته نامه با شماره پیاپی سال 2001
Abstract :
An affinity capillary electrophoresis/laser-induced fluorescence (CE/LIF) assay was developed for direct and specific detection of reverse transcriptase (RT) of the type 1 human immunodeficiency virus (HIV-1) using fluorescently labeled single-stranded DNA aptamers as probes. The aptamer used (RT 26) is specific for HIV-1 RT, and it exhibited no crossreactivity with RTs of the enhanced avian myeloblastosis virus (AMV), the Moloney murine leukemia virus (MMLV), or denatured HIV-1 RT. An affinity complex of RT 26-HIV-1 RT was readily formed, and calibration curves were linear up to 50 nM (6 mug/mL) HIV-1 RT concentration, with both the free probe and complex peak usable for analytical quantitation. Cell culture media (RPMI with 10% fetal bovine serum) interfered with the assay and aptamer-HIV-1 RT binding. Nonspecific binding was observed in low or undiluted culture, necessitating at least 100-fold dilution for analysis of raw culture samples.
Keywords :
High-performance liquid chromatography-mass spectrometry (LC-MS) , Solid-phase extraction (SPE) , Trifolium pratense , red clover , Isoflavone glycoside 6"-O-malonates , Isoflavone glycoside 6"-O-acetates
Journal title :
Analytical Chemistry
Journal title :
Analytical Chemistry