SIMPLIFIED COLORIMETRIC ANALYSIS OF POLYMERASE CHAIN-REACTIONS - DETECTION OF HIV SEQUENCES IN AIDS PATIENTS

被引:41
作者
KEMP, DJ
CHURCHILL, MJ
SMITH, DB
BIGGS, BA
FOOTE, SJ
PETERSON, MG
SAMARAS, N
DEACON, NJ
DOHERTY, R
机构
[1] AMRAD LTD,KEW,VIC 3101,AUSTRALIA
[2] FAIRFIELD HOSP,MACFARLANE BURNET CTR MED RES,FAIRFIELD,VIC 3078,AUSTRALIA
关键词
amplified DNA assay; avidin-peroxidase; biotin; diagnostics; DNA-binding protein GCN4; glutathione S-transferase; oligodeoxyribonucleotides; Recombinant DNA; Taq-polymerase;
D O I
10.1016/0378-1119(90)90391-4
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
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 simultaneouly, 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. © 1990.
引用
收藏
页码:223 / 228
页数:6
相关论文
共 11 条
[1]  
Erlich H.A., 1989, PCR TECHNOLOGY
[2]   EVIDENCE FOR TRANSLATIONAL REGULATION OF THE ACTIVATOR OF GENERAL AMINO-ACID CONTROL IN YEAST [J].
HINNEBUSCH, AG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (20) :6442-6446
[3]   A SENSITIVE NONISOTOPIC HYBRIDIZATION ASSAY FOR HIV-1 DNA [J].
KELLER, GH ;
HUANG, DP ;
MANAK, MM .
ANALYTICAL BIOCHEMISTRY, 1989, 177 (01) :27-32
[4]   COLORIMETRIC DETECTION OF SPECIFIC DNA SEGMENTS AMPLIFIED BY POLYMERASE CHAIN REACTIONS [J].
KEMP, DJ ;
SMITH, DB ;
FOOTE, SJ ;
SAMARAS, N ;
PETERSON, MG .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (07) :2423-2427
[5]   A METHOD FOR THE RAPID SCREENING OF HUMAN-BLOOD SAMPLES FOR THE PRESENCE OF HIV-1 SEQUENCES - THE PROBE-SHIFT ASSAY [J].
KUMAR, R ;
GOEDERT, JJ ;
HUGHES, SH .
AIDS RESEARCH AND HUMAN RETROVIRUSES, 1989, 5 (03) :345-354
[6]   IDENTIFICATION OF HUMAN-IMMUNODEFICIENCY-VIRUS SEQUENCES BY USING INVITRO ENZYMATIC AMPLIFICATION AND OLIGOMER CLEAVAGE DETECTION [J].
KWOK, S ;
MACK, DH ;
MULLIS, KB ;
POIESZ, B ;
EHRLICH, G ;
BLAIR, D ;
FRIEDMANKIEN, A ;
SNINSKY, JJ .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1690-1694
[7]  
LAURE F, 1988, LANCET, V2, P538
[8]   ENZYMATIC AMPLIFICATION OF BETA-GLOBIN GENOMIC SEQUENCES AND RESTRICTION SITE ANALYSIS FOR DIAGNOSIS OF SICKLE-CELL ANEMIA [J].
SAIKI, RK ;
SCHARF, S ;
FALOONA, F ;
MULLIS, KB ;
HORN, GT ;
ERLICH, HA ;
ARNHEIM, N .
SCIENCE, 1985, 230 (4732) :1350-1354
[9]   PRIMER-DIRECTED ENZYMATIC AMPLIFICATION OF DNA WITH A THERMOSTABLE DNA-POLYMERASE [J].
SAIKI, RK ;
GELFAND, DH ;
STOFFEL, S ;
SCHARF, SJ ;
HIGUCHI, R ;
HORN, GT ;
MULLIS, KB ;
ERLICH, HA .
SCIENCE, 1988, 239 (4839) :487-491
[10]   A RAPID SEMI-AUTOMATED MICROTITER PLATE METHOD FOR ANALYSIS AND SEQUENCING BY PCR FROM BACTERIAL STOCKS [J].
SCHOFIELD, JP ;
VAUDIN, M ;
KETTLE, S ;
JONES, DSC .
NUCLEIC ACIDS RESEARCH, 1989, 17 (22) :9498-9498