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DNA-ENC SYNCELLS

DNA Lattice-Encoded Information for Genotype-to-Phenotype Evolution of Self-Replicating Synthetic Cells

Total Cost €

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EC-Contrib. €

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Partnership

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 DNA-ENC SYNCELLS project word cloud

Explore the words cloud of the DNA-ENC SYNCELLS project. It provides you a very rough idea of what is the project "DNA-ENC SYNCELLS" about.

nanotechnology    arranged    max    populations    adding    division    mechanically    specifying    replicating    assembled    enc    3d    rate    shaping    supervised    compartmentalisation    biology    synergy    cytoskeleton    autonomous    first    envisioned    tissue    realised    life    syncells    cycles    tile    joachim    perspectives    chip    evolutionary    serve    scission    machines    pressures    darwinian    biophysics    framework    multiple    subjected    artificial    hosted    replication    microfluidics    broad    completely    planck    encodes    types    stiff    substrates    applicability    sequentially    transport    subsequent    trajectory    vitro    mechanics    initiated    lattice    evolution    inheritable    made    host    variations    repair    synthetic    vivo    microfluidic    profiting    genome    principles    self    cells    within    phenotype    pathogen    mechanical    cellular    act    soft    expertise    cargo    materials    recognition    interdisciplinary    prof    heterogeneous    lipogenesis    dna    compartments    enzymes    bioprinting    man    time    tiles    career    quality    fundamental    influence    catalysts    fellowship    spatz    heidelberg    bits    programmable    medical   

Project "DNA-ENC SYNCELLS" data sheet

The following table provides information about the project.

Coordinator
MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV 

Organization address
address: HOFGARTENSTRASSE 8
city: MUENCHEN
postcode: 80539
website: n.a.

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 Germany [DE]
 Project website http://www.kerstin-goepfrich.de
 Total cost 159˙460 €
 EC max contribution 159˙460 € (100%)
 Programme 1. H2020-EU.1.3.2. (Nurturing excellence by means of cross-border and cross-sector mobility)
 Code Call H2020-MSCA-IF-2017
 Funding Scheme MSCA-IF-EF-ST
 Starting year 2018
 Duration (year-month-day) from 2018-03-01   to  2020-02-29

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    MAX-PLANCK-GESELLSCHAFT ZUR FORDERUNG DER WISSENSCHAFTEN EV DE (MUENCHEN) coordinator 159˙460.00

Map

 Project objective

Within the framework of DNA-ENC SYNCELLS I will develop a synthetic inheritable genome capable of Darwinian evolution which encodes for the phenotype of self-replicating synthetic cells. The defining principles of life, namely compartmentalisation, replication and evolution, will thus be realised in a completely synthetic system for the first time. Two types of DNA tiles – a stiff and a soft tile – arranged in a lattice will serve as bits of information, replicating, without any enzymes, via mechanical scission. The DNA lattice will further act as an artificial cytoskeleton specifying the mechanics and shaping the phenotype of synthetic compartments assembled on a microfluidic chip. After sequentially adding the DNA tiles and catalysts for lipogenesis, the synthetic cells will be subjected to multiple growth and mechanically initiated division cycles. Variations in the mechanical properties will influence the division rate and thus lead to evolution in heterogeneous populations. The evolutionary trajectory of the system will be studied under different selection pressures. Within this two-year fellowship, hosted at the Max Planck Institute for Medical Research in Heidelberg and supervised by Prof. Joachim Spatz, I will contribute to the fundamental knowledge of synthetic cells and enhance its applicability using programmable man-made materials. Greatly profiting from the synergy between my expertise on DNA nanotechnology and the host’s high-quality research on microfluidics, synthetic biology and biophysics, this interdisciplinary project will open up broad perspectives for cellular machines capable of autonomous cargo transport, pathogen recognition or as substrates for 3D-bioprinting and tissue repair in vitro and in vivo – the envisioned focus of my subsequent career in research.

 Publications

year authors and title journal last update
List of publications.
2019 Alexander Ohmann, Kerstin Göpfrich, Himanshu Joshi, Rebecca F Thompson, Diana Sobota, Neil A Ranson, Aleksei Aksimentiev, Ulrich F Keyser
Controlling aggregation of cholesterol-modified DNA nanostructures
published pages: 11441-11451, ISSN: 0305-1048, DOI: 10.1093/nar/gkz914
Nucleic Acids Research 47/21 2020-03-25
2018 Kerstin Göpfrich, Ilia Platzman, Joachim P. Spatz
Mastering Complexity: Towards Bottom-up Construction of Multifunctional Eukaryotic Synthetic Cells
published pages: , ISSN: 0167-7799, DOI: 10.1016/j.tibtech.2018.03.008
Trends in Biotechnology 2020-03-25
2018 Barbara Haller, Kerstin Göpfrich, Martin Schröter, Jan-Willi Janiesch, Ilia Platzman, Joachim P. Spatz
Charge-controlled microfluidic formation of lipid-based single- and multicompartment systems
published pages: , ISSN: 1473-0197, DOI: 10.1039/C8LC00582F
Lab on a Chip 2020-03-25
2019 Kerstin Göpfrich, Barbara Haller, Oskar Staufer, Yannik Dreher, Ulrike Mersdorf, Ilia Platzman, Joachim P. Spatz
One-Pot Assembly of Complex Giant Unilamellar Vesicle-Based Synthetic Cells
published pages: , ISSN: 2161-5063, DOI: 10.1021/acssynbio.9b00034
ACS Synthetic Biology 2020-03-25
2019 Kevin Jahnke, Marian Weiss, Christoph Frey, Silvia Antona, Jan‐Willi Janiesch, Ilia Platzman, Kerstin Göpfrich, Joachim P. Spatz
Programmable Functionalization of Surfactant‐Stabilized Microfluidic Droplets via DNA‐Tags
published pages: 1808647, ISSN: 1616-301X, DOI: 10.1002/adfm.201808647
Advanced Functional Materials 2020-03-25

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