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Membrane-coated 3D architectures for bottom-up synthetic biology
One of the great challenges of bottom-up synthetic biology is to recreate the cellular geometry and surface functionality required for biological reactions. Of particular interest are lipid membrane interfaces where many protein functions take place. However, cellular 3D geometries are often complex...
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Published in: | Soft matter 2021-06, Vol.17 (22), p.5456-5466 |
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creator | Eto, Hiromune Franquelim, Henri G Heymann, Michael Schwille, Petra |
description | One of the great challenges of bottom-up synthetic biology is to recreate the cellular geometry and surface functionality required for biological reactions. Of particular interest are lipid membrane interfaces where many protein functions take place. However, cellular 3D geometries are often complex, and custom-shaping stable lipid membranes on relevant spatial scales in the micrometer range has been hard to accomplish reproducibly. Here, we use two-photon direct laser writing to 3D print microenvironments with length scales relevant to cellular processes and reactions. We formed lipid bilayers on the surfaces of these printed structures, and we evaluated multiple combinatorial scenarios, where physiologically relevant membrane compositions were generated on several different polymer surfaces. Functional dynamic protein systems were reconstituted
in vitro
and their self-organization was observed in response to the 3D geometry. This method proves very useful to template biological membranes with an additional spatial dimension, and thus allows a better understanding of protein function in relation to the complex morphology of cells and organelles.
This paper outlines a robust method to template biological membranes in 3D geometries using micron-scale 3D printing. Dynamic protein systems were reconstituted
in vitro
and their self-organization was observed in response to the 3D geometry. |
doi_str_mv | 10.1039/d1sm00112d |
format | article |
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in vitro
and their self-organization was observed in response to the 3D geometry. This method proves very useful to template biological membranes with an additional spatial dimension, and thus allows a better understanding of protein function in relation to the complex morphology of cells and organelles.
This paper outlines a robust method to template biological membranes in 3D geometries using micron-scale 3D printing. Dynamic protein systems were reconstituted
in vitro
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in vitro
and their self-organization was observed in response to the 3D geometry. This method proves very useful to template biological membranes with an additional spatial dimension, and thus allows a better understanding of protein function in relation to the complex morphology of cells and organelles.
This paper outlines a robust method to template biological membranes in 3D geometries using micron-scale 3D printing. Dynamic protein systems were reconstituted
in vitro
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in vitro
and their self-organization was observed in response to the 3D geometry. This method proves very useful to template biological membranes with an additional spatial dimension, and thus allows a better understanding of protein function in relation to the complex morphology of cells and organelles.
This paper outlines a robust method to template biological membranes in 3D geometries using micron-scale 3D printing. Dynamic protein systems were reconstituted
in vitro
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source | Royal Society of Chemistry:Jisc Collections:Royal Society of Chemistry Read and Publish 2022-2024 (reading list) |
subjects | Biological membranes Biology Combinatorial analysis Cytology Direct laser writing Interfaces Lipid bilayers Lipid membranes Lipids Membrane proteins Membranes Microenvironments Organelles Polymers Proteins Synthetic biology Three dimensional printing |
title | Membrane-coated 3D architectures for bottom-up synthetic biology |
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