Kukura invented mass photometry, a label-free interferometric-scattering microscopy technique that mass-images single biomolecules in solution with precision rivalling native mass spectrometry; his group continues to expand the technique's hardware, analysis (including deep learning) and range of biomolecular applications, in close collaboration with Justin Benesch.

Lemke holds the chair of Synthetic Biophysics at JGU and is adjunct director at the Institute of Molecular Biology. The group's signature is combining genetic code expansion -- installing non-canonical amino acids so a dye can be clicked onto one chosen residue -- with single-molecule fluorescence: smFRET on intrinsically disordered proteins, super-resolution imaging of the nuclear pore complex and its FG-nucleoporin permeability barrier, and engineered membraneless organelles used as designer compartments in living cells. The result is single-molecule-resolution measurement of conformational dynamics and phase behaviour inside cells rather than in vitro. Relative to the established NV-ensemble quantum-sensing playbook (DEER, nanoscale NMR, T1 relaxometry at pT/sqrt(Hz) ensemble sensitivity), this is the strongest biosensing/advanced-microscopy host in Mainz: the labelling chemistry is precisely what a quantum-sensing postdoc would need to attach nanodiamonds or spin labels to a defined protein site, and the group already operates at the single-molecule sensitivity limit optically. Large, well-funded, internationally recruiting group.

Liu's group sits at the junction of DNA nanotechnology and nanophotonics: DNA-origami-templated plasmonic assemblies, reconfigurable artificial nanomachines whose motion is read out optically (chiral plasmonics, FRET), and, increasingly, synthetic-cell systems -- DNA-based pores and a programmable DNA-origami nanosyringe for directed membrane translocation, the latter published jointly with Nussberger's biophysics group at Stuttgart. The through-line is building nanoscale machines that both actuate and report. Relative to the established NV-ensemble quantum-sensing playbook (DEER, nanoscale NMR, T1 relaxometry at pT/sqrt(Hz) ensemble sensitivity), the relevance is on the biosensing axis: this is the group that can put a nanoscale probe exactly where you want it on or through a membrane, which is the delivery problem that in-cell quantum sensing keeps running into. Preferred-attribute note: nanofabrication is heavily used, but the emphasis is on single-molecule optical readout rather than device manufacture per se.

Develops quantum sensing platforms at the biology interface. Core NV-center work: (1) widefield NV magnetic imaging of action potentials in neurons and cardiac tissue; (2) NV-based single-molecule NMR at 14 T resolving molecular structure with single-molecule sensitivity; (3) charge-sensitive shallow NV nanoprobes monitoring real-time cellular electrophysiology; (4) biocompatible diamond surface functionalization enabling multiplexed DNA microarray biosensing; (5) fluorescent-protein spin qubits as biological alternatives to diamond NV (2025 paper, Physics World Top-10 Breakthrough). Runs full NV stack: hot implantation, widefield and confocal ODMR, T1/T2/Hahn echo/DEER/Rabi, automated fitting pipelines. 2026 Sloan Fellow. PhD Lukin/Harvard; postdoc Chu/Stanford. Argonne joint appointment.

Metivier (PPSM) studies photochromic and fluorescent molecules at the single-molecule level - photoswitching kinetics, energy transfer and orientation-resolved imaging - underpinning super-resolution (RESOLFT/STORM-type) probes and molecular sensors. In the broader landscape of NV-centre ensemble quantum sensing (DEER, nano-NMR, T1 relaxometry) operating near pT/sqrt(Hz) sensitivity, this work is paralleled by molecular photoswitches enabling optical super-resolution.

Nobel laureate W. E. Moerner, who first detected and studied single molecules optically, now develops engineered point-spread-function and orientation-resolved single-molecule localization microscopy methods to track individual biomolecules and their rotational dynamics in cells with nanometer precision, well beyond the optical diffraction limit.

Monzel holds the biophysics/biophotonics professorship at Stuttgart's 2nd Institute of Physics. The group develops multiparametric imaging spectroscopy and high-resolution light microscopy -- combining super-resolution, fluorescence-fluctuation and lifetime-resolved methods -- to read out several observables at once in living cells and in biomimetic model membranes, and pairs this with magnetic nanoparticles used to apply and sense forces on cell-surface receptors (magnetogenetic control of signalling). Single-molecule analysis inside cells is an explicit focus. Relative to the established NV-ensemble quantum-sensing playbook (DEER, nanoscale NMR, T1 relaxometry at pT/sqrt(Hz) ensemble sensitivity), this is the closest thing at Stuttgart to a natural biological host for in-cell quantum sensing: the group already does single-molecule-resolution live-cell imaging and already works with magnetic nanoparticles, so nanodiamond relaxometry/thermometry would slot in with the readout stack it already runs. Relatively new appointment -- good moment to join.

Mulvaney directs the ARC Centre of Excellence in Exciton Science and runs Melbourne's nanoscience laboratory. The group's distinctive capability is single-particle and single-emitter optical spectroscopy: photon-antibunching and blinking statistics from individual quantum dots and perovskite nanocrystals, photothermal and dark-field spectroscopy of individual metal nanoparticles, and the electrochemical control of single-nanocrystal charge state. Applications run from LEDs and solar cells to quantum-dot probes for single-particle tracking in cells. Positioned against the established body of NV-ensemble quantum sensing work — DEER, nanoscale NMR and T1 relaxometry protocols operating at pT/sqrt(Hz) field sensitivity — his single-emitter photon-statistics measurements share the shot-noise-limited photon-counting methodology of NV-ensemble ODMR readout, and the group's nanocrystal probes are direct competitors/complements to nanodiamond in cellular sensing. Large, well-resourced group.

Nussberger holds the biophysics chair at Stuttgart's Institute of Biomaterials and Biomolecular Systems. The group studies how proteins cross and insert into membranes -- mitochondrial protein translocases (TOM complex), apoptosis-related pore formation -- using single-channel electrophysiology, single-molecule fluorescence and structural methods, and has pushed this into an explicit nanopore/biosensing line: engineered protein and DNA-based pores as single-molecule sensors, including the DNA-origami nanosyringe for directed membrane translocation published with Na Liu's group. Relative to the established NV-ensemble quantum-sensing playbook (DEER, nanoscale NMR, T1 relaxometry at pT/sqrt(Hz) ensemble sensitivity), the relevance is the readout channel: nanopore sensing is the electrical single-molecule counterpart to optical single-molecule detection, and the group's membrane expertise is exactly what an in-cell quantum-sensing project needs when the question becomes how to get the probe across a bilayer.

Prigozhin develops multicolor electron microscopy using cathodoluminescent nanoprobe protein tags and time-resolved cryo-vitrification methods to capture the nanoscale, sub-second dynamics of GPCR signaling and biomolecular condensate formation, aiming to add molecular-scale color and temporal resolution to electron microscopy's inherent nanoscale spatial resolution.