A nanobody-based toolset to investigate the role of protein localization and dispersal in <i>Drosophila</i>.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 28395731.
- Also identified by DOI 10.7554/eLife.22549 and PMC identifier 5388529.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
The role of protein localization along the apical-basal axis of polarized cells is difficult to investigate in vivo, partially due to lack of suitable tools. Here, we present the GrabFP system, a collection of four nanobody-based GFP-traps that localize to defined positions along the apical-basal axis. We show that the localization preference of the GrabFP traps can impose a novel localization on GFP-tagged target proteins and results in their controlled mislocalization. These new tools were used to mislocalize transmembrane and cytoplasmic GFP fusion proteins in the <i>Drosophila</i> wing disc epithelium and to investigate the effect of protein mislocalization. Furthermore, we used the GrabFP system as a tool to study the extracellular dispersal of the Decapentaplegic (Dpp) protein and show that the Dpp gradient forming in the lateral plane of the <i>Drosophila</i> wing disc epithelium is essential for patterning of the wing imaginal disc.
Medical subject headings
- Drosophila
- Drosophila Proteins
- Entomology
- Molecular Biology
- Protein Transport
- Single-Domain Antibodies