BIOLUMINESCENT DETECTION OF RNA WITH SEQUENCE-SPECIFICITY USING RNA-BINDING PROTEIN-LUCIFERASE FUSION PROTEIN

被引:5
|
作者
KAJITA, Y
KOBATAKE, E
ISHIKAWA, F
AIZAWA, M
机构
[1] TOKYO INST TECHNOL,FAC BIOSCI & BIOTECHNOL,DEPT BIOENGN,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
[2] TOKYO INST TECHNOL,FAC BIOSCI & BIOTECHNOL,DEPT LIFE SCI,MIDORI KU,YOKOHAMA,KANAGAWA 226,JAPAN
关键词
RNA BINDING PROTEIN; FIREFLY LUCIFERASE; FUSION PROTEIN; BIFUNCTIONAL REAGENT; BIOLUMINESCENT DETECTION;
D O I
10.1016/0168-1656(95)00136-2
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A novel bifunctional reagent has been synthesized for RNA detection by genetic fusion of a sequence-specific RNA binding protein and firefly luciferase. The RNA binding protein used in this study recognizes the oligoribonucleotide rH4 which contains four (UUAGGG)-repeat sequence, while luciferase works as a bioluminescent marker. The constructed fusion protein exhibited both sequence-specific RNA binding and bioluminescent activities. The rH4 and rECGF, which has an unrelated sequence having the same length as rH4, were immobilized on a nylon membrane. The membrane was pre-treated by 5% bovine serum albumin and soaked into a fusion protein solution. Bioluminescent detection has successfully been performed at more than 50 pmol of rH4, so the detection limit using this protein was 50 pmol. However, no appreciable bioluminescence was induced by rECGF.
引用
收藏
页码:63 / 70
页数:8
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