Literature DB >> 2258054

Simplified colorimetric analysis of polymerase chain reactions: detection of HIV sequences in AIDS patients.

D J Kemp1, M J Churchill, D B Smith, B A Biggs, S J Foote, M G Peterson, N Samaras, N J Deacon, R Doherty.   

Abstract

We have previously described a colorimetric test, designated an amplified DNA assay (ADA), for specific segments of DNA amplified by polymerase chain reactions (PCRs), suited to diagnostic applications. This relied on binding the amplified DNA via a sequence in one oligodeoxyribonucleotide (oligo) to the DNA-binding protein GCN4 coated on the wells of a microtiter dish. Avidin-peroxidase was then bound to biotin at the 5' end of the other oligo and detected colorimetrically. Two successive PCRs with nested oligos were utilized. We describe here several modifications that greatly simplify the ADA. First, we bind the DNA to a glutathione S-transferase-GCN4 fused polypeptide (GST-GCN4) and avidin-peroxidase simultaneously, rather than successively. Second, we carry out the two successive PCRs in the one reaction mixture, using the thermal stabilities of oligos of differing lengths to separate the two reactions. Third, PCRs can be performed in the wells of a microtiter dish and the amplified DNA captured and detected via GST-GCN4 immobilized on beads attached to the lid of the microtiter dish. Hence it is only necessary to pipette the DNA sample once, and up to 96 samples can then be handled simultaneously.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2258054     DOI: 10.1016/0378-1119(90)90391-4

Source DB:  PubMed          Journal:  Gene        ISSN: 0378-1119            Impact factor:   3.688


  9 in total

Review 1.  Real-time PCR in virology.

Authors:  Ian M Mackay; Katherine E Arden; Andreas Nitsche
Journal:  Nucleic Acids Res       Date:  2002-03-15       Impact factor: 16.971

2.  Sensitivity and specificity of PCR for detection of Mycobacterium tuberculosis: a blind comparison study among seven laboratories.

Authors:  G T Noordhoek; A H Kolk; G Bjune; D Catty; J W Dale; P E Fine; P Godfrey-Faussett; S N Cho; T Shinnick; S B Svenson
Journal:  J Clin Microbiol       Date:  1994-02       Impact factor: 5.948

3.  Clinically practical seminested PCR for Burkholderia pseudomallei quantitated by enzyme immunoassay with and without solution hybridization.

Authors:  M Kunakorn; R B Markham
Journal:  J Clin Microbiol       Date:  1995-08       Impact factor: 5.948

4.  Progress toward a simplified polymerase chain reaction and its application to diagnosis of tuberculosis.

Authors:  S M Wilson; R McNerney; P M Nye; P D Godfrey-Faussett; N G Stoker; A Voller
Journal:  J Clin Microbiol       Date:  1993-04       Impact factor: 5.948

5.  PCR as a confirmatory test for human immunodeficiency virus type 1 infection in individuals with indeterminate western blot (immunoblot) profiles.

Authors:  S Y Sethoe; A E Ling; E H Sng; E H Monteiro; R K Chan
Journal:  J Clin Microbiol       Date:  1995-11       Impact factor: 5.948

6.  Detection of amplified Chlamydia trachomatis DNA using a microtiter plate-based enzyme immunoassay.

Authors:  J M Ossewaarde; M Rieffe; G J van Doornum; C J Henquet; A M van Loon
Journal:  Eur J Clin Microbiol Infect Dis       Date:  1994-09       Impact factor: 3.267

7.  Application of PCR to a clinical and environmental investigation of a case of equine botulism.

Authors:  E A Szabo; J M Pemberton; A M Gibson; R J Thomas; R R Pascoe; P M Desmarchelier
Journal:  J Clin Microbiol       Date:  1994-08       Impact factor: 5.948

8.  Early detection of bovine leukemia virus by using an enzyme-linked assay for polymerase chain reaction-amplified proviral DNA in experimentally infected cattle.

Authors:  H M Naif; R C Daniel; W G Cougle; M F Lavin
Journal:  J Clin Microbiol       Date:  1992-03       Impact factor: 5.948

9.  Improving sensitivity of single tube nested PCR to detect fastidious microorganisms.

Authors:  Diala Shatleh-Rantisi; Asmaa Tamimi; Yaqoub Ashhab
Journal:  Heliyon       Date:  2020-01-27
  9 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.