Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2436129 | International Journal for Parasitology | 2012 | 5 Pages |
Analysis of gene function in Trypanosoma cruzi is limited due to the absence of rapid, simple and reversible genetic tools to regulate gene and corresponding protein expression. We have designed a modified pTREX vector which uses an N-terminal fusion of a ligand-controlled destabilisation domain (ddFKBP) to a gene/protein of interest. This vector allows rapid and reversible protein expression and efficient functional analysis of proteins in different T. cruzi life cycle stages.
Graphical abstractFigure optionsDownload full-size imageDownload high-quality image (46 K)Download as PowerPoint slideHighlights► Regulation of protein expression in Trypanosoma cruzi. ► Modified pTREX vector with a ligand-controlled destabilisation domain. ► Rapid, inducible and reversible. ► Suitable for intracellular form study.