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FACS-optimized mutants of the green fluorescent protein (GFP)

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Cormack, Brendan P., Valdivia, Raphael H., Falkow, Stanley·1996·Gene

Abstract

We have constructed a library in Escherichia coli of mutant gfp genes (encoding green fluorescent protein, GFP) expressed from a tightly regulated inducible promoter. We introduced random amino acid (aa) substitutions in the twenty aa flanking the chromophore Ser-Tyr-Gly sequence at aa 65-67. We then used fluorescence-activated cell sorting (FACS) to select variants of GFP that fluoresce between 20-and 35-fold more intensely than wild type (wt), when excited at 488 nm. Sequence analysis reveals three classes of aa substitutions in GFP. All three classes of mutant proteins have highly shifted excitation maxima. In addition, when produced in E. coli, the folding of the mutant proteins is more efficient than folding of wt GFP. These two properties contribute to a greatly increased (100-fold) fluorescence intensity, making the mutants useful for a number of applications.

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Metadata

Authors
Cormack, B. P., Valdivia, R. H., & Falkow, S.
Venue
Gene
Publisher
Elsevier BV
Published
1996
Volume
173
Issue
1
Pages
33-38
ISSN
0378-1119 (ISSN-L)
OpenAlex
W4233808990
Cited by
2,620
References
0
FWCI
80.80
Type
journal article
Language
en
Open access
hybrid

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CoChat. (2026). Citation check: FACS-optimized mutants of the green fluorescent protein (GFP). https://app.cochat.ai/papers/10.1016/0378-1119(95)00685-0
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Cormack, B. P., Valdivia, R. H., & Falkow, S. (1996). FACS-optimized mutants of the green fluorescent protein (GFP). Gene. https://doi.org/10.1016/0378-1119(95)00685-0

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