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@PHDTHESIS{Prante:44138,
author = {Prante, Olaf},
title = {{S}ynthese des $^{18}${F}-markierten {C}oenzyms
{U}ridindiphosphatglucose als {B}asis für die
$^{18}${F}-{G}lykosylierung von {G}lykoproteinen},
volume = {3902},
issn = {0944-2952},
school = {Univ. Köln},
type = {Dr. (Univ.)},
address = {Jülich},
publisher = {Forschungszentrum Jülich Gmbh Zenralbibliothek, Verlag},
reportid = {PreJuSER-44138, Juel-3902},
series = {Berichte des Forschungszentrums Jülich},
pages = {108 p.},
year = {2001},
note = {Record converted from VDB: 12.11.2012; Köln, Univ., Diss.
2001},
abstract = {The chemo-enzymatic radiosynthesis of no carrier added
(n.c.a.) uridine diphospho-2-deoxy-
2-[$^{18}$F]fluoro-$\alpha$-D-glucose (UDP-[$^{18}$F]FGlc)
was developed. In order to overcome the problem of poor
regioselectivity when using the commonly strategy to label
proteins via $^{18}$F-labelled prosthetic groups, the use of
enzyme systems in addition to the corresponding
$^{18}$F-labelled coenzymes was shown to be a reliable,
regioselective and mild labelling method. With regard to the
comparison and evaluation of the stereoselectivity of the
phosphorylating agents used in the chemical synthesis of
cold uridine diphospho-2-deoxy-2-fluoro-$\alpha$-Dglucose,
$^{31}$P-decoupled and $^{1}$H-NMR-studies were successfully
realized. Uridine diphospho-
2-deoxy-2-fluoro-$\alpha$-D-glucose was obtained in a 7 step
synthesis. Tetrabenzylpyrophosphate was shown to be a highly
stereoselective phosphorylating agent for FDG ($\alpha
/\beta$=3:1). Moreover, a multienzymatic pathway for the
synthesis of uridine diphospho-2-deoxy-2-fluoro-$\alpha$-
D-glucose was adopted starting from FDG and four
commercially available enzymes. This strategy was adjusted
to a mg-scale synthesis providing 35\% chemical yield.
Within the scope of this procedure, a comparison of the
natural substrate $\alpha$-D-glucose-1-phosphate with
2-fluoro-2-deoxy-$\alpha$-D-glucose-1-phosphate indicated
that the enzyme activity of UDP-glucose pyrophosphorylase
(UDP-Glc PPase) was decreased by a factor of 30. With regard
to the adaptability of the multiple enzyme system for the
radiosynthesis of n.c.a. uridine
diphospho-2-deoxy-2-[$^{18}$F]fluoro-$\alpha$-D-glucose a
rapid hexokinase-mediated phosphorylation of [$^{18}$F]FDG
utilizing ATP or UTP as phosphate donor was performed. A
further enzymatic isomerization of n.c.a
[$^{18}$F]FDG-6-phosphate to n.c.a.
[$^{18}$F]FDG-1-phosphate was limited due to the formation
of [$^{18}$F]FDG-1.6-diphosphate as main product.
Experiments using a multiple enzyme system to develop a
fully enzymatic synthetic route to UDP-[$^{18}$F]FGlc turned
out to be less efficient due to the necessity of carrier
added conditions. Thus, a chemo-enzymatic synthesis of
n.c.a. UDP-[$^{18}$8F]FGlc has been developed, starting from
1.3.4.6-tetra-O-acetyl-2-[$^{18}$F]fluoro-2-deoxy-D-glucose,
which occurs as an intermediate in the [$^{18}$F]FDG
synthesis. The chemical phosphorylation via MacDonald
reaction and subsequent deprotection led to a radiochemical
yield of 55\% of [$^{18}$F]FDG-1-phosphate. UDP-
[$^{18}$F]FGlc was synthesized enzymatically by condensation
of [$^{18}$F]FDG-1-phosphate with UTP in presence of UDP-Glc
PPase. In order to overcome the problem of decreased enzyme
acitivty the reaction was performed in a minimized reaction
volume and optimized UTP-concentration of 0.5 mmol/l leading
to an overall radiochemical yield of 20\% of
UDP-[$^{18}$F]FGlc within 110 min. The $^{18}$F-labelled
coenzyme UDP-[$^{18}$F]FGlc was used as a tool for
$^{18}$F-glycosylation of N-acetylglucosamine mediated by
$\beta$-1.4-galactosyltransferase. The $^{18}$F-glycosylated
product was obtained in a radiochemical yield of 56\% and
was easily isolated by solid phase extraction. In addition
to the general availability of [$^{18}$F]FDG worldwide, this
new strategy for enzymatic transfer of "activated
[$^{18}$F]FDG" has demonstrated its potential as a highly
selective and mild $^{18}$F-labelling method of glycosylated
biopolymers to study their pharmacokinetics using
positron-emission-tomography.},
cin = {INC},
cid = {I:(DE-Juel1)VDB53},
pnm = {Radiopharmazeutische Chemie},
pid = {G:(DE-Juel1)FUEK87},
typ = {PUB:(DE-HGF)11 / PUB:(DE-HGF)3},
url = {https://juser.fz-juelich.de/record/44138},
}