The solute carrier superfamily interactome.

溶质载体超家族相互作用组

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作者:Frommelt Fabian, Ladurner Rene, Goldmann Ulrich, Wolf Gernot, Ingles-Prieto Alvaro, Lineiro-Retes Eva, Gelová Zuzana, Hopp Ann-Katrin, Christodoulaki Eirini, Teoh Shao Thing, Leippe Philipp, Santini Brianda L, Rebsamen Manuele, Lindinger Sabrina, Serrano Iciar, Onstein Svenja, Klimek Christoph, Barbosa Barbara, Pantielieieva Anastasiia, Dvorak Vojtech, Hannich Thomas J, Schoenbett Julian, Sansig Gilles, Mocking Tamara A M, Ooms Jasper F, IJzerman Adriaan P, Heitman Laura H, Sykacek Peter, Reinhardt Juergen, Müller André C, Wiedmer Tabea, Superti-Furga Giulio
Solute carrier (SLC) transporters form a protein superfamily that enables transmembrane transport of diverse substrates including nutrients, ions and drugs. There are about 450 different SLCs, residing in a variety of subcellular membranes. Loss-of-function of an unusually high proportion of SLC transporters is genetically associated with a plethora of human diseases, making SLCs a rapidly emerging but challenging drug target class. Knowledge of their protein environment may elucidate the molecular basis for their functional integration with metabolic and cellular pathways and help conceive pharmacological interventions based on modulating proteostatic regulation. We aimed at obtaining a global survey of the SLC-protein interaction landscape and mapped the protein-protein interactions of 396 SLCs by interaction proteomics. We employed a functional assessment based on RNA interference of interactors in combination with measurement of protein stability and localization. As an example, we detail the role of a SLC16A6 phospho-degron and the contributions of PDZ-domain proteins LIN7C and MPP1 to the trafficking of SLC43A2. Overall, our work offers a resource for SLC-protein interactions for the scientific community.

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