Activity-dependent bulk endocytosis proteome reveals a key presynaptic role for the monomeric GTPase Rab11

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 115; no. 43; pp. E10177 - E10186
• Main Authors: Kokotos, A. C., Peltier, J., Davenport, E. C., Trost, M., Cousin, M. A.
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 23.10.2018
• Series: PNAS Plus
• Subjects: Adhesive strength; Animals; Biological Sciences; Cell adhesion; Clathrin; Cytoskeleton; Cytoskeleton - physiology; Endocytosis; Endocytosis - physiology; Endosomes; Endosomes - metabolism; Endosomes - physiology; Female; Fractionation; Guanosine triphosphatases; Nanoparticles; Nanoparticles - metabolism; Network analysis; Neurons; Neurons - metabolism; Neurons - physiology; Neurotransmission; Neurotransmitters; PNAS Plus; Protein Transport - physiology; Proteins; Proteome - metabolism; Proteomes; Proteomics - methods; Protocol (computers); rab GTP-Binding Proteins - metabolism; Rats; Rats, Sprague-Dawley; Synaptic Transmission - physiology; Synaptic Vesicles - metabolism; neuron; endocytosis; vesicle; Rab11; presynapse
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.1809189115

Activity-dependent bulk endocytosis (ADBE) is the dominant mode of synaptic vesicle endocytosis during high-frequency stimulation, suggesting it should play key roles in neurotransmission during periods of intense neuronal activity. However, efforts in elucidating the physiological role of ADBE have been hampered by the lack of identified molecules which are unique to this endocytosis mode. To address this, we performed proteomic analysis on purified bulk endosomes, which are a key organelle in ADBE. Bulk endosomes were enriched via two independent approaches, a classical subcellular fractionation method and isolation via magnetic nanoparticles. There was a 77% overlap in proteins identified via the two protocols, and these molecules formed the ADBE core proteome. Bioinformatic analysis revealed a strong enrichment in cell adhesion and cytoskeletal and signaling molecules, in addition to expected synaptic and trafficking proteins. Network analysis identified Rab GTPases as a central hub within the ADBE proteome. Subsequent investigation of a subset of these Rabs revealed that Rab11 both facilitated ADBE and accelerated clathrin-mediated endocytosis. These findings suggest that the ADBE proteome will provide a rich resource for the future study of presynaptic function, and identify Rab11 as a regulator of presynaptic function.