A sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (anti-human T-cell leukemia virus type I) IgG (anti-HTLV-l IgG) in serum using a synthetic peptide, of HTLV-I, is described. Anti-HTLV-l IgG in test serum, which had been incubated with excess of inactive p-D-galactosida
Immune complex transfer enzyme immunoassay for (anti-human t-cell leukemia virus type i) igg in serum using a synthetic peptide, cys-gag p19(100–130), as antigen
✍ Scribed by Takeyuki Kohno; Dr. Eiji Ishikawa; Iwane Sakoda; Mika Suzuki; Atushi Izumi
- Publisher
- John Wiley and Sons
- Year
- 1991
- Tongue
- English
- Weight
- 936 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0887-8013
No coin nor oath required. For personal study only.
✦ Synopsis
An immune complex transfer enzyme immunoassay for (anti-human T-cell leukemia virus type I) IgG (anti-HTLV-I IgG) in serum using a synthetic peptide, cys-gag p19(100-130), is described. Anti-HTLV-I IgG in test serum, which had been incubated with excess of inactive beta-D-galactosidase to eliminate interference by anti-beta-D-galactosidase antibodies, was reacted simultaneously with 2,4-dinitrophenyl bovine serum albumin-cys-gag p19(100-130) conjugate and cys-gag p19(100-130)-beta-D-galactosidase conjugate. The complex formed of the three components was trapped onto polystyrene balls coated with affinity-purified (anti-2,4-dinitrophenyl group) IgG. After washing to eliminate nonspecific IgG in the test serum and excess of the beta-D-galactosidase conjugate, the complex was eluted from the polystyrene balls with epsilon N-2,4-dinitrophenyl-L-lysine and transferred to polystyrene balls coated with affinity-purified (anti-human IgG gamma-chain) IgG. Beta-D-Galactosidase activity bound to the (anti-human IgG gamma-chain) IgG-coated polystyrene balls was assayed by fluorometry. This assay was 100-fold more sensitive than the conventional enzyme immunoassay, in which a cys-gag p19(100-130)-bovine serum albumin-coated polystyrene ball was incubated with test serum and, after washing, with (anti-human IgG gamma-chain) Fab'-peroxidase conjugate. The degree of inhibition by preincubation of test sera with excess of cys-gag p19(100-130) in combination with an appropriate cut-off value for the fluorescence intensity of bound beta-D-galactosidase activity discriminated almost all seropositive samples from seronegative ones.
📜 SIMILAR VOLUMES
## Abstract A sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (anti‐human T‐cell leukemia virus type 1) IgG (anti‐HTLV‐l IgG) in serum using recombinant gag p24 (14–214) of HTLV‐l is described. The recombinant gag p24(14–214) is soluble in the absence of detergents and
A novel and sensitive enzyme immunoassay (immune-complex-transfer enzyme immunoassay) for antihuman T cell leukemia virustype 1 IgG (anti-HTLV-1 IgG) in human serum using recombinant gag( 14-1 39)-env-(1 97-295) hybrid protein is described. Anti-HTLV-1 IgG in test serum was reacted with dinitropheny
A sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) for (antihuman T-cell leukemia virus type I) IgG (anti-HTLV-l IgG) in serum using a synthetic peptide, Ala-Cys-env gp46(237-262), of HTLV-I is described. Anti-HTLV-l IgG in test serum, which had been incubated with excess of
## Abstract Antibody IgG to human T‐cell leukemia virus type I (HTLV‐I) in urine was detected by a sensitive enzyme immunoassay (immune complex transfer enzyme immunoassay) using a synthetic peptide, Cys‐__env__ gp46(188–224), as antigen, the sensitivity and specificity of which were 100 and 98.5%,