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A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis
A fused gene of the gag and env sequences of human T‐cell leukemia virus type I (HTLV‐I), the causative agent of adult T‐cell leukemia, was constructed in vitro and expressed in Escherichia coli. The gag‐env hybrid protein accumulated as insoluble granules with a yield of approximately 12% of the to...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
1988
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917652/ https://www.ncbi.nlm.nih.gov/pubmed/2465287 http://dx.doi.org/10.1111/j.1349-7006.1988.tb01541.x |
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author | Kuga, Tetsuro Yamasaki, Motoo Sekine, Susumu Fukui, Masanori Yokoo, Yoshiharu Itoh, Seiga Yoshida, Mitsuaki Hattori, Toshio Takatsuki, Kiyoshi |
author_facet | Kuga, Tetsuro Yamasaki, Motoo Sekine, Susumu Fukui, Masanori Yokoo, Yoshiharu Itoh, Seiga Yoshida, Mitsuaki Hattori, Toshio Takatsuki, Kiyoshi |
author_sort | Kuga, Tetsuro |
collection | PubMed |
description | A fused gene of the gag and env sequences of human T‐cell leukemia virus type I (HTLV‐I), the causative agent of adult T‐cell leukemia, was constructed in vitro and expressed in Escherichia coli. The gag‐env hybrid protein accumulated as insoluble granules with a yield of approximately 12% of the total proteins. In an enzyme‐linked immunosorbent assay done with the use of the gag‐env hybrid protein, all 57 seropositive sera gave positive signals, and none of the sera from normal persons did. This system can produce large quantities of the gag‐env hybrid protein, which can be used for mass screening of human sera for HTLV‐I infection. |
format | Online Article Text |
id | pubmed-5917652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1988 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-59176522018-05-11 A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis Kuga, Tetsuro Yamasaki, Motoo Sekine, Susumu Fukui, Masanori Yokoo, Yoshiharu Itoh, Seiga Yoshida, Mitsuaki Hattori, Toshio Takatsuki, Kiyoshi Jpn J Cancer Res Article A fused gene of the gag and env sequences of human T‐cell leukemia virus type I (HTLV‐I), the causative agent of adult T‐cell leukemia, was constructed in vitro and expressed in Escherichia coli. The gag‐env hybrid protein accumulated as insoluble granules with a yield of approximately 12% of the total proteins. In an enzyme‐linked immunosorbent assay done with the use of the gag‐env hybrid protein, all 57 seropositive sera gave positive signals, and none of the sera from normal persons did. This system can produce large quantities of the gag‐env hybrid protein, which can be used for mass screening of human sera for HTLV‐I infection. Blackwell Publishing Ltd 1988-11 /pmc/articles/PMC5917652/ /pubmed/2465287 http://dx.doi.org/10.1111/j.1349-7006.1988.tb01541.x Text en |
spellingShingle | Article Kuga, Tetsuro Yamasaki, Motoo Sekine, Susumu Fukui, Masanori Yokoo, Yoshiharu Itoh, Seiga Yoshida, Mitsuaki Hattori, Toshio Takatsuki, Kiyoshi A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title | A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title_full | A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title_fullStr | A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title_full_unstemmed | A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title_short | A gag‐env Hybrid Protein of Human T‐cell Leukemia Virus Type I and Its Application to Serum Diagnosis |
title_sort | gag‐env hybrid protein of human t‐cell leukemia virus type i and its application to serum diagnosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5917652/ https://www.ncbi.nlm.nih.gov/pubmed/2465287 http://dx.doi.org/10.1111/j.1349-7006.1988.tb01541.x |
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