Summary
Kinesin-1 transports cellular cargos along microtubules as part of neuronal transport. The localisation of kinesin-1 in neurons is tightly controlled to ensure the coordinated delivery of specific cargoes to the regions where they are required. One mechanism of control is through microtubule regulation, but the details of this are not well understood. It has recently been shown that microtubule lattice spacing influences kinesin-1 localisation in U2OS cells. However, the role lattice spacing plays in neuronal transport is unclear. This project aims to investigate features of kinesin-1 based neuronal transport on multiple scales. First, this project aims to use cryo-electron microscopy (cryo-EM) to elucidate how kinesin-1 binds to specific microtubule subsets. I will resolve the high-resolution cryo-EM structure of a dimeric kinesin-1 construct (stableMARK) bound to microtubules with different lattice states. This will explain its lattice specificity and help uncover the mechanics of kinesin-1 walking. Secondly, I will map microtubule lattice spacing in neurons using in situ cryo-electron tomography to establish the lattice diversity within this complex microtubule network. Thirdly, I will use cryo-correlative light electron microscopy and stableMARK to determine if lattice spacing influences kinesin-1 localisation in neurons. This project will answer key biological questions on cytoskeletal transport, which will be applicable to other microtubule-based motors and microtubule associated proteins. Defects in kinesin-1 based transport have been implicated in multiple neuropathies, such as Alzheimer’s disease, therefore further understanding of how neuronal transport is controlled will help uncover the mechanism of these diseases.
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| Web resources: | https://cordis.europa.eu/project/id/101153345 |
| Start date: | 15-04-2024 |
| End date: | 14-04-2026 |
| Total budget - Public funding: | - 187 624,00 Euro |
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Original description
Kinesin-1 transports cellular cargos along microtubules as part of neuronal transport. The localisation of kinesin-1 in neurons is tightly controlled to ensure the coordinated delivery of specific cargoes to the regions where they are required. One mechanism of control is through microtubule regulation, but the details of this are not well understood. It has recently been shown that microtubule lattice spacing influences kinesin-1 localisation in U2OS cells. However, the role lattice spacing plays in neuronal transport is unclear. This project aims to investigate features of kinesin-1 based neuronal transport on multiple scales. First, this project aims to use cryo-electron microscopy (cryo-EM) to elucidate how kinesin-1 binds to specific microtubule subsets. I will resolve the high-resolution cryo-EM structure of a dimeric kinesin-1 construct (stableMARK) bound to microtubules with different lattice states. This will explain its lattice specificity and help uncover the mechanics of kinesin-1 walking. Secondly, I will map microtubule lattice spacing in neurons using in situ cryo-electron tomography to establish the lattice diversity within this complex microtubule network. Thirdly, I will use cryo-correlative light electron microscopy and stableMARK to determine if lattice spacing influences kinesin-1 localisation in neurons. This project will answer key biological questions on cytoskeletal transport, which will be applicable to other microtubule-based motors and microtubule associated proteins. Defects in kinesin-1 based transport have been implicated in multiple neuropathies, such as Alzheimer’s disease, therefore further understanding of how neuronal transport is controlled will help uncover the mechanism of these diseases.Status
SIGNEDCall topic
HORIZON-MSCA-2023-PF-01-01Update Date
24-11-2024
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