Comparison of mutant forms of the green fluorescent protein as expression markers in Chinese hamster ovary (CHO) and Saccharomyces cerevisiae cells

被引:24
作者
Natarajan, A
Subramanian, S
Srienc, F
机构
[1] Univ Minnesota, Dept Chem Engn & Mat Sci, Minneapolis, MN USA
[2] Univ Minnesota, Biol Proc Technol Inst, St Paul, MN 55108 USA
基金
美国国家科学基金会;
关键词
green fluorescent protein; Chinese hamster ovary; Saccharomyces cerevisiae;
D O I
10.1016/S0168-1656(98)00040-6
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
Several green fluorescent protein (Gfp) mutants with increased cellular fluorescence compared to the wildtype protein have recently been generated. We have expressed and compared wildtype Gfp and mutants S65T, F100S/ M154T/V164A, F64L/S65T, and S65A/V68L/S72A under identical growth conditions in CHO and Saccharomyces cerevisiae cells. The results suggest that the last two Gfp mutants are the best candidates as reporter proteins, and they provide a high signal-to-noise ratio in both systems. Single gene copy expression of these mutant forms is easily detectable over background autofluorescence. All Gfps are highly stable within cells, with an estimated 1/2-life between 7 h (wildtype) and 70 h (F100S/M154T/V164A) in S. cerevisiae cells. Although this limits their use in examining rapid cellular events without further modification, Gfp is expected to be a useful marker for monitoring the physiological state of cells in bioreactors using on-line probes. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:29 / 45
页数:17
相关论文
共 33 条
[1]   Simultaneous fluorescence-activated cell sorter analysis of two distinct transcriptional elements within a single cell using engineered green fluorescent proteins [J].
Anderson, MT ;
Tjioe, IM ;
Lorincz, MC ;
Parks, DR ;
Herzenberg, LA ;
Nolan, GP ;
Herzenberg, LA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (16) :8508-8511
[2]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[3]   FACS-optimized mutants of the green fluorescent protein (GFP) [J].
Cormack, BP ;
Valdivia, RH ;
Falkow, S .
GENE, 1996, 173 (01) :33-38
[4]   Improved green fluorescent protein by molecular evolution using DNA shuffling [J].
Crameri, A ;
Whitehorn, EA ;
Tate, E ;
Stemmer, WPC .
NATURE BIOTECHNOLOGY, 1996, 14 (03) :315-319
[5]   UNDERSTANDING, IMPROVING AND USING GREEN FLUORESCENT PROTEINS [J].
CUBITT, AB ;
HEIM, R ;
ADAMS, SR ;
BOYD, AE ;
GROSS, LA ;
TSIEN, RY .
TRENDS IN BIOCHEMICAL SCIENCES, 1995, 20 (11) :448-455
[6]   RED-SHIFTED EXCITATION MUTANTS OF THE GREEN FLUORESCENT PROTEIN [J].
DELAGRAVE, S ;
HAWTIN, RE ;
SILVA, CM ;
YANG, MM ;
YOUVAN, DC .
BIO-TECHNOLOGY, 1995, 13 (02) :151-154
[7]  
DIEN BS, 1994, METHOD CELL BIOL, V42, P457
[8]   GREEN-FLUORESCENT PROTEIN MUTANTS WITH ALTERED FLUORESCENCE EXCITATION-SPECTRA [J].
EHRIG, T ;
OKANE, DJ ;
PRENDERGAST, FG .
FEBS LETTERS, 1995, 367 (02) :163-166
[9]   DYNAMICS OF ACTIVATION OF A GALACTOSE-INDUCIBLE PROMOTER IN SACCHAROMYCES-CEREVISIAE [J].
EITZMAN, PD ;
SRIENC, F .
JOURNAL OF BIOTECHNOLOGY, 1991, 21 (1-2) :63-82
[10]   WAVELENGTH MUTATIONS AND POSTTRANSLATIONAL AUTOXIDATION OF GREEN FLUORESCENT PROTEIN [J].
HEIM, R ;
PRASHER, DC ;
TSIEN, RY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (26) :12501-12504