Abstract
Transient associations between numerous organelles - e.g., the endoplasmic reticulum and the mitochondria - forge highly-coordinated, particular environments essential for cross-compartment information flow. Our perspective summarizes chemical-biology tools that have enabled identifying proteins present within these itinerant communities against the bulk proteome, even when a particular protein's presence is fleeting/substoichiometric. However, proteins resident at these ephemeral junctions also experience transitory changes to their interactomes, small-molecule signalomes, and, importantly, functions. Thus, a thorough census of sub-organellar communities necessitates functionally probing context-dependent signaling properties of individual protein-players. Our perspective accordingly further discusses how repurposing of existing tools could allow us to glean a functional understanding of protein-specific signaling activities altered as a result of organelles pulling together. Collectively, our perspective strives to usher new chemical-biology techniques that could, in turn, open doors to modulate functions of specific subproteomes/organellar junctions underlying the nuanced regulatory subsystem broadly termed as contactology. This journal is
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CITATION STYLE
Long, M. J. C., Zhao, Y., & Aye, Y. (2020, June 1). Neighborhood watch: Tools for defining locale-dependent subproteomes and their contextual signaling activities. RSC Chemical Biology. Royal Society of Chemistry. https://doi.org/10.1039/d0cb00041h
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