Ardavan leads the Quantum Spin Dynamics group, studying quantum coherent phenomena in condensed matter. Central to the lab's quantum sensing relevance: (1) molecular spin qubits — using pulsed EPR/DEER to characterise and control multi-spin registers ({Cr7Ni} molecular rings, nitroxide radical chains) assembled into qubit networks, measuring coherence times, inter-qubit couplings, and demonstrating spin-electric coupling in molecular magnets; (2) DNA-assembled molecular quantum devices — using DNA nanostructures to precisely position molecular spin qubits for multi-qubit sensing and quantum information applications; (3) surface atom spin resonance — STM-based coherent spin control of individual atoms on surfaces at nanosecond timescales. Uses X-band through W-band pulsed EPR at Centre for Advanced Electron Spin Resonance (CAESR), Oxford.

Boecking leads the Molecular Machines Group and is acting director of the EMBL Australia Node in Single Molecule Science. The group reconstitutes molecular machines — clathrin coat disassembly, HIV capsid assembly and uncoating, pore-forming toxins — and watches them work one molecule at a time by TIRF, interferometric scattering (mass photometry) and fluorescence fluctuation methods, resolving short-lived intermediates that ensemble kinetics averages into invisibility. He trained originally in surface chemistry and biosensors with Gooding, which gives the group unusual competence in engineering the surfaces these assays run on. 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 — the argument for single-molecule methods over ensemble ones is identical to the argument for pushing NV sensing below its pT/sqrt(Hz) ensemble regime: the interesting biology lives in heterogeneity and in transient states that averaging destroys. Strong methodological neighbour for a quantum-biosensing candidate.

Dickinson's group develops advanced optical microscopy methods for biological and biomedical imaging. Research directions: (1) STORM super-resolution microscopy — stochastic optical reconstruction for nanoscale imaging of biological structures at ~20 nm lateral resolution; imaging cytoskeletal dynamics, cellular organelles, and pathological structures; (2) Optical coherence tomography (OCT) — depth-resolved, label-free imaging for biomedical diagnostics (retinal, cardiovascular tissues); (3) Laser speckle imaging — blood flow and perfusion measurements in tissues; (4) Multiphoton microscopy — second harmonic generation (SHG) and two-photon for collagen structure imaging in connective tissues and cancer. Part of the Manchester Photon Science Institute biophotonics theme.

Fletcher combines optical and force microscopy (AFM, optical tweezers) with purified-protein and single-cell assays to measure the mechanics of cell movement and immune-cell activation, and has also developed low-cost imaging instrumentation (foldscopes, phone-based microscopes) for global health.

Gambardella leads the Magnetism and Interface Physics group at ETH D-MATL. Research directions: (1) Scanning probe magnetometry — using NV-center cantilevers (collaboration with Degen) and magneto-optical Kerr microscopy to image spin textures (skyrmions, domain walls) in thin-film heterostructures with sub-100 nm resolution; (2) Spin-orbit torques — current-induced magnetization switching via interfacial spin-orbit coupling; spin Hall and Rashba effects for spintronic devices; (3) Single-atom magnetism — STM and X-ray absorption for element-specific orbital and spin moments of individual atoms on surfaces; (4) XMCD at synchrotron — quantitative element-specific magnetic spectroscopy. Quantum sensing angle: spin-orbit driven phenomena, high-resolution magnetic imaging.

Hoogenboom leads a biophysics group at UCL specializing in high-speed atomic force microscopy. Research directions: (1) High-speed AFM — imaging conformational dynamics of DNA, proteins (including membrane channels), and chromatin at ms time resolution and sub-nm spatial resolution in aqueous conditions; (2) Nuclear pore complex — mapping transport selectivity and structure of NPCs in native nuclear envelopes using AFM; (3) Antimicrobial mechanisms — imaging membrane disruption by antimicrobial peptides in real time; (4) AFM-based force spectroscopy — measuring single-molecule interaction forces in chromatin and protein assemblies. Strong relevance to biological sensing at the single-molecule level.

Pioneers living bioelectronics integrating semiconductor nanostructures with biological systems. Primary directions: (1) silicon nanowire / nanoporous silicon photoelectrochemical interfaces for optical neuromodulation with subcellular spatial resolution; (2) intracellular silicon nanowire probes for recording action potentials from individual organelles; (3) bioinspired flexible mesh electronics for in vivo neural and cardiac interfaces. QuBBE member. 2026 Marian and Stuart Rice Research Award.

Willem Vanderlinden uses high-resolution biophysical tools to study protein-nucleic acid interactions. Research: (1) magnetic tweezers for pN-scale force and torque measurements on single DNA molecules and nucleoprotein complexes during retroviral integration, DNA supercoiling, and chromatin remodelling; (2) high-speed AFM imaging of nucleoprotein complexes and chromosomal organisation; (3) quantitative single-molecule statistical analysis of DNA topology. His approach provides cutting-edge spatial resolution to study chromatin biophysics and mobile DNA elements at the single-molecule level.

Wickham builds DNA origami nanostructures — programmable, self-assembling scaffolds with nanometre-precision addressability — and uses them as molecular machines, drug-delivery vehicles and, most relevantly, as rulers and probes for single-molecule measurement. DNA origami is the standard platform for DNA-PAINT super-resolution and for positioning fluorophores, nanoparticles or spin labels at defined separations, and her group works on dynamic, reconfigurable devices that respond to biological triggers. 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 — DNA origami is the leading candidate technology for positioning target molecules at a controlled standoff from a near-surface NV ensemble, which is the central geometric problem in pushing NV nanoscale NMR and DEER from pT/sqrt(Hz) ensembles down to single-molecule sensitivity. Genuinely complementary skill set for a quantum-sensing candidate.