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Table 6.3 Fluorescent peptide and protein biosensors of protein kinases—cont'd
Protein kinase
Biosensor features
Author and year
Reference
Green/14-3-3 phosphoserine
binding domain
PKA, PKC, p38,
MAPKAP K2,
Akt, Erk1, Src
Micelle/auto-assembly
Sun
et al.
(2005)
131
Ratio metric strategies
PKA
Single probe/wavelength shift/
phosphorylation-sensitive Cd
(II)-cylcen aminocoumarin
Kikuchi
et al.
2009
132
Src
Dual probe/merocyanine and
mCerulean
Gulyani
et al.
(2011)
112
Photoactivatable biosensors
PKC
NBD probe proximal to
phosphorylation site, caged
serine
Veldhuyzen
et al.
(2003)
110
PKC beta
NBD probe proximal to
phosphorylation site, caged
serine
Dai
et al.
(2007)
133
Src
Self-reporting biosensor, caged
tyrosine
Wang
et al.
(2006)
127
when coupled to peptide biosensors for biological applications have been
readily characterized by several groups of chemists (see Ref.
105
and refer-
ences therein). Although most of these probes possess excellent photo-
physical properties for
in vitro
applications, their excitation and emission
wavelengths tend to be incompatible with
in vivo
applications. Notwith-
standing, several groups of chemists are currently devoting their effort to
synthesize environmentally sensitive red-shifted dyes with suitable proper-
ties for
in vivo
sensing applications.
Environmentally sensitive kinase biosensors constitute a unique class of sen-
sors in that they rely on changes in the environment of the fluorescent probe to
report on phosphorylation of the kinase biosensor. Different means have been
employed to achieve this goal: phosphorylation itself, phosphorylation-induced
conformational changes, and binding of
the phosphorylation site by a
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