Proteomic characterization of the Alzheimer's disease risk factor BIN1 interactome
Joseph D. McMillaniD, Shuai WangiD, Jessica WohlfahrtiD, Jennifer GuerguesiD, Stanley M. StevensiD, Gopal ThinakaraniD
Abstract
The gene BIN1 is the second-largest genetic risk factor for late-onset Alzheimer's disease (LOAD). It is expressed in neurons and glia in the brain as cell-type specific and ubiquitous isoforms. BIN1 is an adaptor protein that regulates membrane dynamics in many cell types. Previously, we reported that BIN1 predominantly localizes to presynaptic terminals in neurons and regulates presynaptic vesicular release. However, the function of neuronal BIN1 in relation to LOAD is not yet fully understood. A significant gap in the field is the unbiased characterization of neuronal BIN1-interacting proteins and proximal neighbors. To address this gap and help define the functions of neuronal BIN1 in the brain, we employed TurboID-based proximity labeling to identify proteins biotinylated by the neuronal BIN1 isoform 1-TurboID fusion protein (BIN1iso1-TID) in cultured mouse neuroblastoma (N2a) cells in vitro and in adult mouse brain neurons in vivo. Label-free quantification-based proteomic analysis of the BIN1iso1-TID biotinylated proteins led to the discovery of 361 proteins in N2a cells and 897 proteins in mouse brain neurons, identified as BIN1iso1-associated (proximal) or interacting proteins. A total of 92 proteins were common in both datasets, indicating that these are high-confidence BIN1-interacting or proximity proteins. SynapticGO analysis of the mouse brain dataset revealed that BIN1iso1-TurboID labeled 159 synaptic proteins, with 60 corresponding to the synaptic vesicle cycle. Based on phosphorylation site analysis of the neuronal BIN1iso1-TID interactome and related kinase prediction, we selected AAK1, CDK16, SYNJ1, PP2BA, and RANG for validation through immunostaining and proximity ligation assays as members of the BIN1 interactome in the mouse brain. By identifying several previously unknown proximal and potential interacting proteins of BIN1, this study establishes a foundation for further investigations into the function of neuronal BIN1.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 4
- FWCI
- 2.55
- Field percentile
- top 10%
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- BIN1 protein isoforms are differentially expressed in astrocytes, neurons, and microglia: neuronal and astrocyte BIN1 implicated in Tau pathology
M. Taga, V. A. Petyuk, … P. L. De Jager·bioRxiv·Jan 31, 2019
- Loss of the Alzheimer’s-linked bridging integrator 1 (BIN1) protein affects synaptic structure and disrupts tau localisation and release
Elizabeth B. C. Glennon, Dawn H. W. Lau, … Wendy J. Noble·Brain CommunicationsPeer-reviewed·Jan 1, 2020
- Alzheimer's disease risk gene BIN1 induces Tau-dependent network hyperexcitability
Yuliya Voskobiynyk, Jonathan R. Roth, … Erik D. Roberson·eLifePeer-reviewed·Jul 13, 2020
- BIN1 recovers tauopathy-induced long-term memory deficits in mice and interacts with Tau through Thr348 phosphorylation
Maxime Sartori, Tiago Mendes, … Jean‐Charles Lambert·Acta NeuropathologicaPeer-reviewed·May 7, 2019
- BIN1 expression in the presynaptic compartment leads to isoform-specific synaptotoxicity
Erwan Lambert, Carla Gelle, … Pierre Dourlen·bioRxiv·Aug 11, 2025
- The Alzheimer susceptibility gene BIN1 induces isoform-dependent neurotoxicity through early endosome defects
Erwan Lambert, Orthis Saha, … Pierre Dourlen·Acta Neuropathologica CommunicationsPeer-reviewed·Jan 8, 2022