RT Journal Article SR Electronic T1 Topology-Driven Discovery of Transmembrane Protein S-Palmitoylation JF bioRxiv FD Cold Spring Harbor Laboratory SP 2024.09.08.611865 DO 10.1101/2024.09.08.611865 A1 Forrester, Michael T. A1 Egol, Jacob R. A1 Ozbay, Sinan A1 Singh, Rohit A1 Tata, Purushothama Rao YR 2024 UL http://biorxiv.org/content/early/2024/09/08/2024.09.08.611865.abstract AB Protein S-palmitoylation is a reversible lipophilic posttranslational modification regulating a diverse number of signaling pathways. Within transmembrane proteins (TMPs), S-palmitoylation is implicated in conditions from inflammatory disorders to respiratory viral infections. Many small-scale experiments have observed S-palmitoylation at juxtamembrane Cys residues. However, most large-scale S-palmitoyl discovery efforts rely on trypsin-based proteomics within which hydrophobic juxtamembrane regions are likely underrepresented. Machine learning– by virtue of its freedom from experimental constraints – is particularly well suited to address this discovery gap surrounding TMP S-palmitoylation. Utilizing a UniProt-derived feature set, a gradient boosted machine learning tool (TopoPalmTree) was constructed and applied to a holdout dataset of viral S-palmitoylated proteins. Upon application to the mouse TMP proteome, 1591 putative S-palmitoyl sites (i.e. not listed in SwissPalm or UniProt) were identified. Two lung-expressed S-palmitoyl candidates (synaptobrevin Vamp5 and water channel Aquaporin-5) were experimentally assessed. Finally, TopoPalmTree was used for rational design of an S-palmitoyl site on KDEL-Receptor 2. This readily interpretable model aligns the innumerable small-scale experiments observing juxtamembrane S-palmitoylation into a proteomic tool for TMP S-palmitoyl discovery and design, thus facilitating future investigations of this important modification.Competing Interest StatementThe authors have declared no competing interest.