Research



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Our goal is to investigate and control complex chemical and biological systems by using and devloping new methods and materials. Very often we make use of nanomaterials as building blocks to engineer functional materials. These materials are able to collect information or trigger processes from (bio)chemical systems and finally biological functions. Below you can find some examples of recently published work.

We thank for generous funding from the DFG, FCI, EXC 171, CNMPB, VW Stiftung, MWK Lower Saxony, life@nano.

 

1. New materials, surface chemistry and photophysics

Nanomaterials are versatile building blocks for nanoscale sensors and actuators because they share the same length scale as many biological structures. Additionally, the low-dimensionality and quantum-confinement very often results in interesting and unique physical and chemical properties. We study optoelectronic properties of materials to understand fundamental mechanisms and to identify materials that provide properties for completely new applications.


Among the different nanomaterials carbon nanomaterials have many extremely useful characteristics and provide rich structural, optical and chemical diversity. For example, carbon nanotubes are hollow cylinders of one-atom-thick sheets of carbon. All these properties and their size make carbon nanotubes ideal materials for different types of biomedical applications (Advanced Drug Delivery Reviews 2013, Analytical and Bioanalytical Chemistry 2016). One of our goals is to understand the photophysics of carbon nanotubes and to use them for biosensing (JPC 2016).

 

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2. Near Infrared spectroscopy and microscopy

The near infrared (nIR) is a special region of the electromagnetic spectrum. Humans cannot see it and it falls into the tissue-transparency window because nIR light can penetrate deeper into tissue. We use and develop near infrared spectroscopy to study new materials. For example, carbon nantotubes display fluorescence in the nIR and nIR spectroscopy and microscopy is useful to study basic mechanism such as the structure of biomolecules on their surface (JPC 2016, JACS 2014, PNAS 2017).

3. Chemical imaging and biosensors

Chemical imaging is a powerful concept. It provides spatiotemporal information about sample. A typical example is Raman spectroscopy-based imaging. We develop fluorescent nanosensors and use many of them to image molecules with high spatiotemporal resolution. At present, direct optical detection of neurotransmitter changes around neurons is an unsolved issue. Therefore many aspects of chemical neurotransmission remain unexplored, which hampers understanding the brain. We have recently developed the first carbon nanotube-based fluorescent sensor of dopamine in the near infrared (JACS 2014) and used it to image dopamine release from cells (PNAS 2017). A key challenge to create fast, selective and sensitive nanosensors is controlling the organic phase around the nanomaterial (Nature Nano 2013, JPC 2016).

 

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Figure 2: Imaging neurotransmitter release with fluorescent nanosensors. From PNAS 2017.

The organic corona determines how an analyte interacts with e.g. the carbon nanotube and how it affects the optoelectronic properties. This topic is directly related to understanding in general how molecules interact with the organic (corona) phase around nanoparticles and influence their optoelectronic properties. Our long-term goal is to use these and other label-free optical sensors to map neurotransmitter release events in neural circuits and immunological systems and gain fundamental new insights into chemical communication between cells.

 

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Figure 3: Monte-Carlo simulations of fluorescent sensors reveal resolution limits and provide mechanistic insights. From ACS Nano 2017.

We furthermore use theoretical methods to explore the resolution limits of imaging with nanosensors (see figure 3). Such simulations help us to understand how a perfect sensor should be designed and which biological processes are resolvable (ACS Nano 2017).

4. Cell Biophysics

Neutrophilic granulocytes are able to release their own DNA as neutrophil extracellular traps (NETs) to capture and eliminate pathogens. DNA expulsion (NETosis) has also been documented for other cells and organisms, thus highlighting the evolutionary conservation of this process. Moreover, dysregulated NETosis has been implicated in many diseases, including cancer and inflammatory disorders. During NETosis, neutrophils undergo dynamic and dramatic alterations of their cellular as well as sub-cellular morphology whose biophysical basis is poorly understood. Here we investigate NETosis in real-time on the single-cell level using fluorescence and atomic force microscopy. Our results show that NETosis is highly organized into three distinct phases with a clear point of no return defined by chromatin status. Entropic chromatin swelling is the major physical driving force that causes cell morphology changes and the rupture of both nuclear envelope and plasma membrane. Through its material properties, chromatin thus directly orchestrates this complex biological process (Neubert, Meyer et al. Nat. Commun., 2018).

 

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