Proteomics of protein trafficking by in vivo tissue-specific labeling.

Autor: Droujinine, Ilia A., Meyer, Amanda S., Wang, Dan, Udeshi, Namrata D., Hu, Yanhui, Rocco, David, McMahon, Jill A., Yang, Rui, Guo, JinJin, Mu, Luye, Carey, Dominique K., Svinkina, Tanya, Zeng, Rebecca, Branon, Tess, Tabatabai, Areya, Bosch, Justin A., Asara, John M., Ting, Alice Y., Carr, Steven A., McMahon, Andrew P.
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Zdroj: Nature Communications; 4/22/2021, Vol. 12 Issue 1, p1-22, 22p
Abstrakt: Conventional approaches to identify secreted factors that regulate homeostasis are limited in their abilities to identify the tissues/cells of origin and destination. We established a platform to identify secreted protein trafficking between organs using an engineered biotin ligase (BirA*G3) that biotinylates, promiscuously, proteins in a subcellular compartment of one tissue. Subsequently, biotinylated proteins are affinity-enriched and identified from distal organs using quantitative mass spectrometry. Applying this approach in Drosophila, we identify 51 muscle-secreted proteins from heads and 269 fat body-secreted proteins from legs/muscles, including CG2145 (human ortholog ENDOU) that binds directly to muscles and promotes activity. In addition, in mice, we identify 291 serum proteins secreted from conditional BirA*G3 embryo stem cell-derived teratomas, including low-abundance proteins with hormonal properties. Our findings indicate that the communication network of secreted proteins is vast. This approach has broad potential across different model systems to identify cell-specific secretomes and mediators of interorgan communication in health or disease. The network of proteins secreted for interorgan communication is poorly understood. Here, the authors develop a method, based on protein labeling, to study cell-specific secretomes and interorgan protein trafficking, and demonstrate their approach in Drosophila and mouse models. [ABSTRACT FROM AUTHOR]
Databáze: Complementary Index
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