Robert Nißler

Dr. Robert Nißler


Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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25 November 2020 in Nature Communications
Verified
Journal Article
Open access
PDF file
RNRobert Nißler
Robert Nißler
OBOliver Bader
Oliver Bader
MDMaria Dohmen
Maria Dohmen
SWSebastian G. Walter
Sebastian G. Walter
CNChristine Noll
Christine Noll
SKSebastian Kruss
Sebastian Kruss
Infectious diseases are worldwide a major cause of morbidity and mortality. Fast and specific detection of pathogens such as bacteria is needed to combat these diseases. Optimal methods would be non-invasive and without extensive sample-taking/processing. Here, we developed a set of near infrared (NIR) fluorescent nanosensors and used them for remote fingerprinting of clinically important bacteria. The nanosensors are based on single-walled carbon nanotubes (SWCNTs) that fluoresce in the NIR optical tissue transparency window, which offers ultra-low background and high tissue penetration. They are chemically tailored to detect released metabolites as well as specific virulence factors (lipopolysaccharides, siderophores, DNases, proteases) and integrated into functional hydrogel arrays with 9 different sensors. These hydrogels are exposed to clinical isolates of 6 important bacteria (Staphylococcus aureus, Escherichia coli,…) and remote (≥25 cm) NIR imaging allows to identify and distinguish bacteria. Sensors are also spectrally encoded (900 nm, 1000 nm, 1250 nm) to differentiate the two major pathogens P. aeruginosa as well as S. aureus and penetrate tissue (>5 mm). This type of multiplexing with NIR fluorescent nanosensors enables remote detection and differentiation of important pathogens and the potential for smart surfaces.

8 April 2021 in Analytical Chemistry
Verified
Journal Article
Closed access
RNRobert Nißler
Robert Nißler
LKLarissa Kurth
Larissa Kurth
HLHan Li
Han Li
ASAlexander Spreinat
Alexander Spreinat
IKIlyas Kuhlemann
Ilyas Kuhlemann
SKSebastian Kruss
Sebastian Kruss

11 August 2021 in The Journal of Physical Chemistry C
Verified
Journal Article
Closed access
ASAlexander Spreinat
Alexander Spreinat
MDMaria M. Dohmen
Maria M. Dohmen
JLJan Lüttgens
Jan Lüttgens
NHNiklas Herrmann
Niklas Herrmann
LKLars F. Klepzig
Lars F. Klepzig
SKSebastian Kruss
Sebastian Kruss

5 October 2021 in Angewandte Chemie International Edition
Verified
Journal Article
Open access
PDF file
RNRobert Nißler
Robert Nißler
AMAndrea Teresa Müller
Andrea Teresa Müller
FDFrederike Dohrman
Frederike Dohrman
LKLarissa Kurth
Larissa Kurth
HLHan Li
Han Li
SKSebastian Kruss
Sebastian Kruss
Plants use secondary metabolites such as polyphenols for chemical defense against pathogens and herbivores. Despite their importance in plant pathogen interactions and tolerance to diseases, it remains challenging to detect polyphenols in complex plant tissues. Here, we create molecular sensors for plant polyphenol imaging that are based on near‐infrared (NIR) fluorescent single‐wall carbon nanotubes (SWCNTs). We identified polyethylene glycol–phospholipids that render (6,5)‐SWCNTs sensitive (Kd=90 nM) to plant polyphenols (tannins, flavonoids, …), which red‐shift (up to 20 nm) and quench their emission (ca. 1000 nm). These sensors report changes in total polyphenol level after herbivore or pathogen challenge in crop plant systems (Soybean Glycine max) and leaf tissue extracts (Tococa spp.). We furthermore demonstrate remote chemical imaging of pathogen‐induced polyphenol release from roots of soybean seedlings over the time course of 24 h. This approach allows in situ visualization and understanding of the chemical plant defense in real time and paves the way for plant phenotyping for optimized polyphenol secretion.

29 April 2023 in Cancers
Verified
Journal Article
Open access
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SWSebastian Walter
Sebastian Walter
PKPeter Knöll
Peter Knöll
PEPeer Eysel
Peer Eysel
AQAlexander Quaas
Alexander Quaas
CGChristopher Gaisendrees
Christopher Gaisendrees
LHLena Hieggelke
Lena Hieggelke
Chondrosarcoma (CHS) are heterogenous, but as a whole, represent the second most common primary malignant bone tumor entity. Although knowledge on tumor biology has grown exponentially during the past few decades, surgical resection remains the gold standard for the treatment of these tumors, while radiation and differentiated chemotherapy do not result in sufficient cancer control. An in-depth molecular characterization of CHS reveals significant differences compared to tumors of epithelial origin. Genetically, CHS are heterogenous, but there is no characteristic mutation defining CHS, and yet, IDH1 and IDH2 mutations are frequent. Hypovascularization, extracellular matrix composition of collagen, proteoglycans, and hyaluronan create a mechanical barrier for tumor suppressive immune cells. Comparatively low proliferation rates, MDR-1 expression and an acidic tumor microenvironment further limit therapeutic options in CHS. Future advances in CHS therapy depend on the further characterization of CHS, especially the tumor immune microenvironment, for improved and better targeted therapies.

24 June 2021 in Nanoscale Advances
Verified
Journal Article
Open access
PDF file
GSGabriele Selvaggio
Gabriele Selvaggio
MWMilan Weitzel
Milan Weitzel
NONazar Oleksiievets
Nazar Oleksiievets
TOTabea A. Oswald
Tabea A. Oswald
RNRobert Nißler
Robert Nißler
SKSebastian Kruss
Sebastian Kruss
Egyptian Blue (CaCuSi4O10, EB), Han Blue (BaCuSi4O10, HB) and Han Purple (BaCuSi2O6, HP) are exfoliated into 2D nanosheets (NS). Near-infrared (NIR) fluorescence properties are reported and (lifetime) imaging applications are demonstrated.