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CSDP

Construction of Self-Dividing Protocells

Total Cost €

0

EC-Contrib. €

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Partnership

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Project "CSDP" data sheet

The following table provides information about the project.

Coordinator
STICHTING KATHOLIEKE UNIVERSITEIT 

Organization address
address: GEERT GROOTEPLEIN NOORD 9
city: NIJMEGEN
postcode: 6525 EZ
website: www.radboudumc.nl

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country Netherlands [NL]
 Project website http://www.ru.nl/physicalorganicchemistry/
 Total cost 177˙598 €
 EC max contribution 177˙598 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2014
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2015
 Duration (year-month-day) from 2015-08-01   to  2017-07-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    STICHTING KATHOLIEKE UNIVERSITEIT NL (NIJMEGEN) coordinator 177˙598.00

Map

 Project objective

Artificial cells are synthetic compartments that are able to mimic one or more properties of natural cells and provide valuable avenues for the study of fundamental cellular functions. However, thus far there are no examples of synthetic systems/materials that can achieve self-replication. Therefore the key aim of this project is to create artificial self-dividing protocells. I will build a platform that combines synthetic chemistry, cell biology and microfluidics to prepare cell-like systems. Monodisperse picoliter multiple all-aqueous droplet systems (e.g., liposomes) generated by microfluidics will be utilized to construct self-dividing protocells. To achieve division, the so-called Z-ring of the bacterial divisome will be incorporated in droplets, together with an energy-generation system. I have extensive experience in microfluidics research and especially in the preparation of multiple emulsions with complex compartments, which I will exploit in this project. At Radboud University (RU), I will obtain new skills and expertise in biochemistry and biology such as in vitro gene expression, chemical reaction networks, and bottom-up synthetic biology. Importantly, the reconstitution of an artificial cell divisome would lead to a deeper understanding of the biophysical principles of cellular behavior and will be the most fundamental step towards construction of artificial cells. I believe this in vitro reconstituted system provides a revolutionary new platform for biomimetic research.

 Publications

year authors and title journal last update
List of publications.
2017 Fei Peng, Nan-Nan Deng, Yingfeng Tu, Jan C. M. van Hest, Daniela A. Wilson
Continuous fabrication of polymeric vesicles and nanotubes with fluidic channels
published pages: 4875-4880, ISSN: 2040-3364, DOI: 10.1039/C7NR00142H
Nanoscale 9/15 2019-06-18
2017 Nan-Nan Deng, Wilhelm T. S. Huck
Microfluidic Formation of Monodisperse Coacervate Organelles in Liposomes
published pages: 9736-9740, ISSN: 1433-7851, DOI: 10.1002/anie.201703145
Angewandte Chemie International Edition 56/33 2019-06-18
2016 Nan-Nan Deng, Maaruthy Yelleswarapu, Wilhelm T. S. Huck
Monodisperse Uni- and Multicompartment Liposomes
published pages: 7584-7591, ISSN: 0002-7863, DOI: 10.1021/jacs.6b02107
Journal of the American Chemical Society 138/24 2019-06-18
2017 Nan-Nan Deng, Maaruthy Yelleswarapu, Lifei Zheng, and Wilhelm T. S. Huck
Microfluidic Assembly of Monodisperse Vesosomes as Artificial Cell Models
published pages: 587-590, ISSN: 0002-7863, DOI: 10.1021/jacs.6b10977
Journal of the American Chemical Society 139/2 2019-06-18

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