SubsidieMeesters logoSubsidieMeesters
ProjectenRegelingenAnalyses

Mechanisims of nuclear self-assembly

The project aims to create synthetic nuclei ('Organelloids') to study the self-assembly mechanisms of the nuclear envelope, enhancing understanding of nuclear function and its implications for diseases.

Subsidie
€ 1.499.974
2024

Projectdetails

Introduction

Shape and function of the vertebrate nucleus depend on the choreographed interplay between lipids, proteins, and DNA to form the nuclear envelope. Even small molecular changes, such as point mutations in the proteins of the nuclear envelope (the lamina), cause detrimental human diseases including premature aging, cancer, and heart disease.

To date, a clear, mechanistically compelling explanation for the dynamic coupling of lipids, proteins, and DNA to safeguard nuclear shape and function is still missing. We here propose to build minimal, synthetic nuclei (‘Organelloids’) bottom-up as a tool to study the self-assembly of a functional nucleus.

Recent Discoveries

We recently discovered the conserved molecular machinery that ensures the assembly of the nuclear envelope in open vertebrate mitosis. Our data point to uncharacterized fundamental mechanisms that couple the following processes:

  1. The fusion of lipid-membrane sheets into a continuous nuclear membrane.
  2. The formation of the lamina.
  3. The organization of chromatin in the same chain of events.

Proposal Overview

In this proposal, we will leverage our recent advances in reconstitution to build ‘Organelloids’ to recapitulate the shape and function of the membrane-lamina-chromatin confluence.

Using these nuclear Organelloids, we will resolve the nuclear assembly process in high resolution by applying integrated structural biology and determine the unknown biophysical principles that drive the self-organization of individual molecules into one functional organelle.

Goals and Implications

Our strategy will reveal the unknown hierarchical relationship between lipids, proteins, and DNA and produce detailed mechanistic models for the formation and coupling of functional subdomains that are commonly observed in the nuclear membrane, the lamina, and chromatin.

With cell models and top-down approaches, we ultimately aim to define the fundamental principles that govern nuclear biogenesis with implications for health and disease.

Financiële details & Tijdlijn

Financiële details

Subsidiebedrag€ 1.499.974
Totale projectbegroting€ 1.499.974

Tijdlijn

Startdatum1-1-2024
Einddatum31-12-2028
Subsidiejaar2024

Partners & Locaties

Projectpartners

  • MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EVpenvoerder

Land(en)

Germany

Inhoudsopgave

European Research Council

Financiering tot €10 miljoen voor baanbrekend frontier-onderzoek via ERC-grants (Starting, Consolidator, Advanced, Synergy, Proof of Concept).

Bekijk regeling

Vergelijkbare projecten binnen European Research Council

ProjectRegelingBedragJaarActie

Reshaping the nucleome to reveal its gene- and mechano-regulatory function

The RENOME project aims to develop tools for real-time study and reengineering of chromatin organization to connect nuclear mechanics with cellular behavior and inform future epigenetic therapies.

ERC Consolid...€ 1.998.595
2025
Details

The geometrical and physical basis of cell-like functionality

The project aims to uncover mechanistic principles for building life-like systems from minimal components using theoretical modeling and in-silico evolution to explore protein patterns and membrane dynamics.

ERC Advanced...€ 2.498.813
2024
Details

Understanding emergent physical properties of chromatin using synthetic nuclei

This project aims to bridge in vitro and cellular studies to elucidate how molecular activities of chromatin influence its material properties and nuclear organization through innovative experimental methods.

ERC Consolid...€ 1.999.550
2023
Details

Recreating molecular memories: imaging the mechanics of chromosome assembly and the birth of cell identity

This project aims to uncover the molecular mechanisms of histone deposition during DNA replication to enhance understanding of epigenetic memory transmission and chromosome assembly.

ERC Consolid...€ 1.999.575
2025
Details

Uncovering the role and regulation of 3D DNA-RNA nuclear dynamics in controlling cell fate decisions

This project aims to elucidate the interplay between 3D genome organization and transcriptome dynamics in early mouse embryos to identify factors influencing cell fate decisions.

ERC Starting...€ 1.500.000
2023
Details
ERC Consolid...

Reshaping the nucleome to reveal its gene- and mechano-regulatory function

The RENOME project aims to develop tools for real-time study and reengineering of chromatin organization to connect nuclear mechanics with cellular behavior and inform future epigenetic therapies.

ERC Consolidator Grant
€ 1.998.595
2025
Details
ERC Advanced...

The geometrical and physical basis of cell-like functionality

The project aims to uncover mechanistic principles for building life-like systems from minimal components using theoretical modeling and in-silico evolution to explore protein patterns and membrane dynamics.

ERC Advanced Grant
€ 2.498.813
2024
Details
ERC Consolid...

Understanding emergent physical properties of chromatin using synthetic nuclei

This project aims to bridge in vitro and cellular studies to elucidate how molecular activities of chromatin influence its material properties and nuclear organization through innovative experimental methods.

ERC Consolidator Grant
€ 1.999.550
2023
Details
ERC Consolid...

Recreating molecular memories: imaging the mechanics of chromosome assembly and the birth of cell identity

This project aims to uncover the molecular mechanisms of histone deposition during DNA replication to enhance understanding of epigenetic memory transmission and chromosome assembly.

ERC Consolidator Grant
€ 1.999.575
2025
Details
ERC Starting...

Uncovering the role and regulation of 3D DNA-RNA nuclear dynamics in controlling cell fate decisions

This project aims to elucidate the interplay between 3D genome organization and transcriptome dynamics in early mouse embryos to identify factors influencing cell fate decisions.

ERC Starting Grant
€ 1.500.000
2023
Details

SubsidieMeesters logoSubsidieMeesters

Vind en verken subsidieprojecten in Nederland en Europa.

Links

  • Projecten
  • Regelingen
  • Analyses

Suggesties

Heb je ideeën voor nieuwe features of verbeteringen?

Deel je suggestie
© 2025 SubsidieMeesters. Alle rechten voorbehouden.