Key result
SWATH-MS identifies 15 unique RACK1-interacting proteins in Drosophila cells, enriching for translation and nucleic acid binding.
Why the study?
A proteomic characterization of the RACK1 interactome in Drosophila S2 cells using SWATH-MS was needed to identify interactants and quantify low abundance proteins.
SWATH-MS provides a significant advantage over DDA in identifying RACK1 interactants and quantifying low abundance proteins in Drosophila S2 cells.
Caution against clinical use of Drosophila data; extends the RACK1 interactome and leaves open mammalian cardiovascular validation.
Receptor for Activated protein C kinase 1 (RACK1) is a scaffold protein that has been found in association with several signaling complexes, and with the 40S subunit of the ribosome. Using the model organism Drosophila melanogaster, we recently showed that RACK1 is required at the ribosome for internal ribosome entry site (IRES)-mediated translation of viruses. Here, we report a proteomic characterization of the interactome of RACK1 in Drosophila S2 cells. We carried out Label-Free quantitation using both Data-Dependent and Data-Independent Acquisition (DDA and DIA, respectively) and observed a significant advantage for the Sequential Window Acquisition of all THeoretical fragment-ion spectra (SWATH) method, both in terms of identification of interactants and quantification of low abundance proteins. These data represent the first SWATH spectral library available for Drosophila and will be a useful resource for the community. A total of 52 interacting proteins were identified, including several molecules involved in translation such as structural components of the ribosome, factors regulating translation initiation or elongation, and RNA binding proteins. Among these 52 proteins, 15 were identified as partners by the SWATH strategy only. Interestingly, these 15 proteins are significantly enriched for the functions translation and nucleic acid binding. This enrichment reflects the engagement of RACK1 at the ribosome and highlights the added value of SWATH analysis. A functional screen did not reveal any protein sharing the interesting properties of RACK1, which is required for IRES-dependent translation and not essential for cell viability. Intriguingly however, 10 of the RACK1 partners identified restrict replication of Cricket paralysis virus (CrPV), an IRES-containing virus.
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Kühn et al. (2017) studied this question. SWATH-MS vs. Data-Dependent Acquisition (DDA) was evaluated on Identification of RACK1 interacting proteins. SWATH-MS analysis of Drosophila S2 cells identified 52 RACK1-interacting proteins, including 15 unique to the SWATH strategy that are enriched for translation and nucleic acid binding functions.
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