A strategy for the generation of non-aggregating mutants of Anthozoa fluorescent proteins.

Abstract:

:Recently, we cloned several fluorescent proteins of different colors homologous to Aequorea victoria green fluorescent protein, which have great biotechnological potential as in vivo markers of gene expression. However, later investigations revealed severe drawbacks in the use of novel fluorescent proteins (FPs), in particular, the formation of tetramers (tetramerization) and high molecular weight aggregates (aggregation). In this report, we employ a mutagenic approach to resolve the problem of aggregation. The elimination of basic residues located near the N-termini of FPs results in the generation of non-aggregating versions of several FPs, specifically, drFP583 (DsRed), DsRed-Timer, ds/drFP616, zFP506, zFP538, amFP486, and asFP595.

journal_name

FEBS Lett

journal_title

FEBS letters

authors

Yanushevich YG,Staroverov DB,Savitsky AP,Fradkov AF,Gurskaya NG,Bulina ME,Lukyanov KA,Lukyanov SA

doi

10.1016/s0014-5793(01)03263-x

keywords:

subject

Has Abstract

pub_date

2002-01-30 00:00:00

pages

11-4

issue

1-3

eissn

0014-5793

issn

1873-3468

pii

S001457930103263X

journal_volume

511

pub_type

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