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Sroka, T. J.

Publications and source records attributed to Sroka, T. J..

2 recordsLinked to original sources

Proximity proteomics of primary cilia in human hypothalamic neurons

Primary cilia are hair-like sensory organelles that project from the cell bodies of most cell types, including appetite-regulatory hypothalamic neurons where they likely help sense metabolic factors to regulate food intake. We hypothesized that characterising the proteins present in the primary cilia of hypothalamic neurons would shed mechanistic insights into their sensory role and identify new therapeutic targets for obesity. We therefore targeted the ascorbate peroxidase APEX2 to primary cilia in human induced pluripotent stem cells (hiPSC)-derived hypothalamic neurons to biotinylate and identify ciliary proteins. Among the cilia-enriched proteins, we identified synaptic proteins, neurotransmitter receptors, and cell-cell adhesion and axon guidance proteins, extending recent findings that primary cilia interact with neuronal synapses. We also found genes associated with increased body weight and metabolic phenotypes that could represent new therapeutic targets including the lysophosphatidic receptor 1 (LPAR1), which we validated is cilia-localized and we confirmed that its ligand (LPA) mediates ciliary shortening. These findings provide insights into the molecular mechanisms by which primary cilia functionally impact appetite-regulatory neurons.

cell biology↗

iAPEX: Improved APEX-based proximity labeling for subcellular proteomics using an enzymatic reaction cascade

Ascorbate peroxidase (APEX) is a versatile labeling enzyme used for live-cell proteomics at high spatial and temporal resolution. However, toxicity of its substrate hydrogen peroxide and background labeling by endogenous peroxidases limit its use to in vitro studies of specific cell types. By combining APEX2 with a D-amino acid oxidase to locally produce hydrogen peroxide, we establish a more versatile, improved APEX (iAPEX) workflow that minimizes hydrogen peroxide toxicity and reduces non-specific background labeling. We employ iAPEX to perform live-cell proteomics of a cellular microdomain, the primary cilium, in previously inaccessible cell lines, leading to the identification of new ciliary proteins. Our study robustly validates common ciliary proteins across two distinct cell lines, while observed differences may reflect heterogeneity in primary cilia proteomes. iAPEX proximity labeling in Xenopus laevis provides a proof-of-concept for future in vivo applications.

biochemistry↗