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The activity of genes in health and disease are manifested through
the proteins which they encode. Ultimately, proteins drive functional
processes in cells and tissues and so by measuring individual protein
levels, studying modifications and discovering their sites of action
we will understand better their function. It is possible to visualise
the location of proteins of interest in tissue sections using labelled
antibodies which bind to the target protein. This procedure, known
as immunohistochemistry, provides valuable information on the cellular
and sub-cellular distribution of proteins in tissue.
Historically
this information set has been created by disparate groups of
workers focusing on one or a few genes of interest. The
coverage of genes by this approach is adhoc, and the information
is not generated or shared in a consistent fashion. The availability
of complete annotated genomes means there are opportunities for
more systematic, co-ordinated approaches to capturing, sharing
and integrating information generated by an individual experimental
approach. The Atlas project aims to create
a quality, information rich database of protein expression profiles
(AtlasDB), which is accessible to the world-wide research community.
The internal consistency and efficiency achieved by executing such
an initiative
in a single location, using optimised and standardised procedures
will add to its value. As well as the long term archival value
of the data, the accompanying validated antibody and protein
clones will potentially have great research, diagnostic and possibly
therapeutic
potential.
The Atlas group expresses recombinant protein and uses these as
antigens to create recombinant antibodies from phage display technology.
The resultant antibodies are used in immunohistochemistry to identify
tissue expression patterns and the images are electronically captured
and annotated.
The 'Atlas of Protein Expression' team have optimised the component
parts of this process, in preparation for running this as a high
throughput process by using tissue microarrys (TMA). In particular we have introduced and developed
high throughput systems that will allow us to examine 1000’s of
tissue samples at a time and capture the results using automated
microscopy.


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