Curated Optogenetic Publication Database

Search precisely and efficiently by using the advantage of the hand-assigned publication tags that allow you to search for papers involving a specific trait, e.g. a particular optogenetic switch or a host organism.

Showing 1 - 3 of 3 results
1.

Light controlled cell-to-cell adhesion and chemical communication in minimal synthetic cells.

blue iLID in vitro Extracellular optogenetics
Chem Commun (Camb), 22 Jul 2019 DOI: 10.1039/c9cc04768a Link to full text
Abstract: Decorating GUVs, used as minimal synthetic cell models, with photoswitchable proteins allows controlling the adhesion between them and their assembly into multicellular structures with light. Thereby, the chemical communication between a sender and a receiver GUV, which strongly depends on their spatial proximity, can also be photoregulated.
2.

Light-Guided Motility of a Minimal Synthetic Cell.

blue iLID in vitro Extracellular optogenetics
Nano Lett, 23 Oct 2018 DOI: 10.1021/acs.nanolett.8b03469 Link to full text
Abstract: Cell motility is an important but complex process; as cells move, new adhesions form at the front and adhesions disassemble at the back. To replicate this dynamic and spatiotemporally controlled asymmetry of adhesions and achieve motility in a minimal synthetic cell, we controlled the adhesion of a model giant unilamellar vesicle (GUV) to the substrate with light. For this purpose, we immobilized the proteins iLID and Micro, which interact under blue light and dissociate from each other in the dark, on a substrate and a GUV, respectively. Under blue light, the protein interaction leads to adhesion of the vesicle to the substrate, which is reversible in the dark. The high spatiotemporal control provided by light, allowed partly illuminating the GUV and generating an asymmetry in adhesions. Consequently, the GUV moves into the illuminated area, a process that can be repeated over multiple cycles. Thus, our system reproduces the dynamic spatiotemporal distribution of adhesions and establishes mimetic motility of a synthetic cell.
3.

Dynamic blue light-switchable protein patterns on giant unilamellar vesicles.

blue iLID in vitro Extracellular optogenetics
Chem Commun (Camb), 23 Jan 2018 DOI: 10.1039/c7cc08758f Link to full text
Abstract: The blue light-dependent interaction between the proteins iLID and Nano allows recruiting and patterning proteins on GUV membranes, which thereby capture key features of patterns observed in nature. This photoswitchable protein interaction provides non-invasive, reversible and dynamic control over protein patterns of different sizes with high specificity and spatiotemporal resolution.
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