Because of these limitations, the AAV approach is best suited for tissue culture based approaches that require
modification of only a
single allele of a
gene, such as the introduction of heterozygous endogenous epitope tags, or the introduction of dominant mutations of a
gene into the endogenous allele
in cultured cells.
«Although the whole proteome representation is simplified by adapting a
gene centric point of view and disregarding post translational
modifications, it still offers the first possibility of a proteome wide view of the autoantibody reactivity
in healthy individuals and persons with autoimmune disorders,
in one
single experiment.»