Functional expression of the Aequorea victoria green fluorescent protein in insect cells using the baculovirus expression system

被引:20
作者
Reilander, H
Hasse, W
Maul, G
机构
[1] Max-Planck-Inst. für Biophysik, Abt. Mol. Membranbiologie, D-60528 Frankfurt/M
关键词
D O I
10.1006/bbrc.1996.0173
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A DNA fragment encoding the green fluorescent protein (GFP) was isolated via FCR from a jellyfish Aequorea victoria cDNA, cloned and sequenced. Subsequently, a recombinant baculovirus bearing the coding region of the GFP under the transcriptional control of the Autographa californica nuclear polyhedrosis virus (AcMNPV) polyhedrin gene promoter was constructed and isolated. High-level expression of GFP could be easily monitored in Spodoptera frugiperda (Sf9) insect cells after infection with recombinant baculovirus, due to the intrinsic fluorescence (lambda(max) = 508 nm) of the recombinant protein Lifter excitation with blue light (lambda(max) = 400 nm). The functional recombinant GFP displayed an apparent molecular mass of approximate to 43 kDa and the fluorescence emission spectrum of the recombinant protein was virtually identical to that of the native green fluorescent protein. (C) 1996 Academic Press, Inc.
引用
收藏
页码:14 / 20
页数:7
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