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Light-Controlled Promiscuous Cell Adhesion through the Plasma Membrane-Binding Protein BcLOV4.

Nivedha Veerasubramanian1, Anne Aalto2, Seraphine V Wegner1

  • 1Institute for Physiological Chemistry and Pathobiochemistry, University of Münster, Münster 48149, Germany.

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|September 22, 2025
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Summary
This summary is machine-generated.

Engineered a synthetic cell adhesion molecule (BcLOV4-PM) for light-controlled cell binding. This innovation enables tissue engineering applications without modifying all cell types involved.

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Area of Science:

  • Cell Biology
  • Biotechnology
  • Biophysics

Background:

  • Dynamic regulation of cell-cell adhesion is crucial for biological processes and tissue engineering.
  • Current optogenetic methods for controlling cell adhesion often necessitate genetic modification of all participating cell types.
  • A need exists for versatile tools that enable precise, cell-type-agnostic control over cell adhesion.

Purpose of the Study:

  • To engineer a novel, single-component synthetic cell adhesion molecule for light-dependent cell-cell interactions.
  • To demonstrate the ability of this molecule to mediate both homotypic and heterotypic cell adhesions.
  • To showcase its utility in light-controlled tissue engineering applications, such as spheroid compaction.

Main Methods:

  • Engineered a synthetic cell adhesion molecule (BcLOV4-PM) by fusing a blue-light-responsive protein (BcLOV4) with a transmembrane domain.
  • Utilized blue light to induce cell-cell adhesions mediated by BcLOV4-PM.
  • Employed temperature changes (37 °C) to disrupt the light-induced adhesions, leveraging BcLOV4's thermosensitivity.
  • Demonstrated light-controlled spheroid compaction in both monocultures and cocultures with unmodified wild-type cells.

Main Results:

  • BcLOV4-PM cells formed light-dependent homotypic and heterotypic adhesions with unmodified wild-type cells.
  • Adhesions were induced by blue light and could be disrupted by elevated temperature (37 °C), but not by darkness.
  • Demonstrated successful light-controlled compaction of spheroids using BcLOV4-PM in mixed cell populations.
  • The engineered molecule facilitated promiscuous and modular control over cell-cell adhesion.

Conclusions:

  • BcLOV4-PM provides a versatile, single-component solution for light-dependent cell-cell adhesion control.
  • This system enables cell adhesion modulation without requiring genetic modification of all interacting cell types.
  • Offers significant potential for advanced applications in tissue engineering and the study of multicellular systems.