Due to the importance of the antigen/ antibody reaction, all hospitals
and blood banks worldwide rely on routine blood group
phenotyping of samples. Using recombinant antigens removes
the disadvantage of the current antibody screening when using
the human red blood cells, which can complicate the detection of
antibody in di erent cases: in the case of multi-transfused individuals
and in the case of weak antigens. Although constructing
recombinant antigens for some blood group antigens has been
achieved successfully, such as; Kell, Du y and Lutheran blood
group antigens, no studies have been published describing successful
production of RH recombinant antigens in a prokaryotic
expression system. Rh proteins are conserved across many different
species.
The aim was to construct a hybrid Rh protein comprised of a
Nitrosomonas europaea (N. europaea) Rh50 backbone containing
di erent external loops of the human RhD protein.
Human RhD external loop 6 was the most suitable candidate
to start with due to its location between highly conserved domains
of the protein. The hybrid gene for the NeRH50"human
RHD was sub-cloned into an expression vector (pET) and transformed
in BL21 (DE3) competent E. coli. We constructed three
other hybrid genes with RhD human external loops on a NeRh50
backbone: loops 4, 6; loops 3, 4, 6 and loops 2, 3, 4, 6.
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Hybrid recombinant constructs were successfully expressed in
the E. coli membrane as shown with western blot,
ow cytometry,
and transmission electron microscopy by the use of di erent
commercial/ customized monoclonal and polyclonal antibodies
against D epitopes in human RhD proteins and NeRh50 like
protein. Due to a lack of time, testing human sera against the
recombinant antigens was not possible. However, the approach
utilised in this study may lead to a new diagnostic assay whereby
the expression of human RhD external loops in E. coli may be
capable of detecting speci c anti-Rh antibodies in patient serum.
Date of Award | 2019 |
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Original language | English |
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Awarding Institution | |
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Supervisor | Tracey Madgett (Other Supervisor) |
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Biochemistry: Production of recombinant Rh blood group antigens for detection of alloimmunisation
Alkhanbashi, M. (Author). 2019
Student thesis: PhD