ZMB Member Barbara Saccà
ZMB Member
Barbara Saccà
Next ZMB-Member
Prof. Dr. Barbara Saccà
Group
BionanotechnologyCenter of Medical Biotechnology (ZMB)
Faculty of Biology
University of Duisburg-Essen
Universitätsstr. 2
45141 Essen
- +49 201 183 3395
- Website
- Press Releases
- Selected Publications
- Publication Metrics
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- ZMB Research Program
Molecular and Chemical Cell Biology
Research Overview
Our main goal is to create programmable nanoscale compartments that emulate essential features of biological systems. By controlling molecular interactions inside these nanosized compartments and across their boundaries, we aim to establish DNA-based nanoarchitectures as powerful tools to dissect, reconstruct, and ultimately engineer biological function from the bottom up.
Research Focus
We investigate the effect of nanoconfinement on (multivalent) binding interactions and analyze how complex formation is affected by the geometric arrangement, flexibility, and stoichiometry of ligands, as well as unspecific electrostatic interactions at the host-guest interface and the presence of molecular crowders.
A particular focus lies on protein behavior within the nanosized lumen. We study how confinement affects the kinetics of enzymes, the motion of molecular motors, and the spatial orientation of proteins under defined geometrical constraints.
Beyond internal processes, we explore how DNA nanocompartments communicate with their surroundings. By engineering the permeability characteristics of these nanochambers, we aim to precisely regulate the entry and exit of molecules and thus control the exchange of information across the compartment boundary.
A recent advancement in our research focuses on the interaction between DNA nanocompartments and lipid bilayers, aiming to integrate these nanodevices in cellular model systems.
Selected Publications
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A modular DNA origami nanocompartment for engineering a cell-free, protein unfolding and degradation pathwayIn: Nature Nanotechnology, Vol. 19, 2024, Nr. 10, pp. 1521 – 1531DOI (Open Access)
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Engineering modular enzymes using DNA origamiIn: Nature Nanotechnology, Vol. 19, 2024, Nr. 10, pp. 1440 – 1441
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The primordial life of DNA dynamic networksIn: Nature Catalysis, Vol. 3, 2020, Nr. 11, pp. 865 – 866
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Sites of high local frustration in DNA origamiIn: Nature Communications, Vol. 10, 2019, Nr. 1, pp. 1061DOI (Open Access)
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Hierarchical Assembly of DNA Filaments with Designer Elastic PropertiesIn: ACS Nano, Vol. 12, 2018, Nr. 1, pp. 44 – 55
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Tailored protein encapsulation into a DNA host using geometrically organized supramolecular interactionsIn: Nature Communications, Vol. 8, 2017, pp. 14472DOI, Online Full Text (Open Access)
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Characterizing the Effect of Multivalent Conjugates Composed of Aβ-Specific Ligands and Metal Nanoparticles on Neurotoxic Fibrillar AggregationIn: ACS Nano, 2016, pp. 7582 – 7597
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Determinants of amyloid fibril degradation by the PDZ protease HTRA1In: Nature Chemical Biology, Vol. 11, 2015, Nr. 11, pp. 862 – 869DOI, Online Full Text (Open Access)
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Reversible reconfiguration of DNA origami nanochambers monitored by single-molecule FRETIn: Angewandte Chemie International Edition, Vol. 54, 2015, Nr. 12, pp. 3592 – 3597
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Site-Directed, on-surface assembly of DNA nanostructuresIn: Angewandte Chemie International Edition, Vol. 54, 2015, Nr. 41, pp. 12039 – 12043
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DNA Origami : The Art of Folding DNAIn: Angewandte Chemie International Edition, Vol. 51, 2012, Nr. 1, pp. 58 – 66
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Functionalization of DNA nanostructures with proteinsIn: Chemical Society Reviews, Vol. 40, 2011, Nr. 12, pp. 5910 – 5921
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Orthogonal Protein Decoration of DNA OrigamiIn: Angewandte Chemie International Edition, Vol. 49, 2010, Nr. 49, pp. 9378 – 9383
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Dendritic DNA Building Blocks for Amplified Detection Assays and BiomaterialsIn: Angewandte Chemie International Edition, Vol. 48, 2009, Nr. 33, pp. 5996 – 6000
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High-Throughput, Real-Time Monitoring of the Self-Assembly of DNA Nanostructures by FRET SpectroscopyIn: Angewandte Chemie International Edition, Vol. 47, 2008, Nr. 11, pp. 2135 – 2137
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Kinetics of tetramolecular quadruplexesIn: Nucleic Acids Research, Vol. 33, 2005, Nr. 1, pp. 81 – 94
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Length-dependent energetics of (CTG)n and (CAG)n trinucleotide repeatsIn: Nucleic Acids Research, Vol. 33, 2005, Nr. 13, pp. 4065 – 4077
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The effect of chemical modifications on the thermal stability of different G-quadruplex-forming oligonucleotidesIn: Nucleic Acids Research, Vol. 33, 2005, Nr. 4, pp. 1182 – 1192
