XB-ART-5881
Genesis
2003 Feb 01;352:107-13. doi: 10.1002/gene.10171.
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Expression of scFv antibodies in Xenopus embryos to disrupt protein function: implications for large-scale evaluation of the embryonic proteome.
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We evaluated the use of single-chain antibody (scFv) expression as a tool to disrupt the function of specific proteins in embryos of the frog, Xenopus laevis. The expression of scFvs that recognize the bone morphogenetic protein receptor (ALK3) or the fibroblast growth factor receptor1 (FGFR1) as endoplasmic reticulum-anchored proteins caused distinct developmental defects that were virtually indistinguishable from the defects caused by expression of the dominant negative forms of each receptor. These results demonstrate that scFvs from phage-display libraries can be readily fashioned into effective and specific inhibitors of signaling pathways in developing embryos. In addition, as several effective scFvs against a specific target can be isolated rapidly, this approach represents a valuable new tool for large-scale functional analysis of the embryonic proteome.
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Species referenced: Xenopus laevis
Genes referenced: bmpr1a erbb2 fgfr1 myf5 ncam1 tbxt
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Phenotypes: Xla Wt + bmpr1a{scFv_D1} (fig.2.a)
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