Ananthanarayanan was awarded the Royal Microscopical Society Life Sciences Award in 2025 for the use of novel microscopies in cell biology. Her group images individual motor proteins — dynein, kinesin — and the mitochondria they transport, in living cells, at single-molecule sensitivity, combining light-sheet and TIRF-class imaging with particle tracking to ask how organelle positioning and mitochondrial dynamics are controlled. The methodological emphasis is on getting single-molecule sensitivity inside a live cell rather than in vitro, which is the hard version of the problem. 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 — this is the closest thing at UNSW to a biological end-user for an in-cell quantum sensor: the mitochondrial systems she studies are precisely where NV nanodiamond thermometry and free-radical relaxometry at pT/sqrt(Hz) have been aimed, and she has the live-cell imaging infrastructure to validate any such measurement independently.

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.

Boxer's group uses vibrational Stark effect spectroscopy -- measuring field-dependent shifts of nitrile, carbonyl, and other IR-active vibrational probes -- to quantify electrostatic fields inside proteins, membranes, and active sites, providing a molecular-scale, spectroscopic route to electric-field sensing distinct from device-based quantum sensors. [Borderline match: a molecular spectroscopic probe of local fields rather than a fabricated quantum sensor; kept for review.]

Branton is a pioneer of nanopore sensing, having shown that single DNA/RNA molecules threading through a nanopore produce ionic-current signatures usable for single-molecule sequencing — foundational work underlying the modern solid-state and biological nanopore-sequencing industry, and a direct fit to the biosensing/single-molecule filter criterion.

Bustamante is a founding figure of single-molecule biophysics, using optical and magnetic tweezers to measure the forces and torques generated by molecular motors (RNA polymerase, viral packaging motors, the ribosome) as they act on individual nucleoprotein complexes. The lab continues to push single-molecule force spectroscopy toward sub-piconewton, millisecond resolution to resolve mechanochemical intermediates invisible to bulk assays.

Nobel laureate Steven Chu's group spans laser cooling/trapping of atoms and single-molecule biophysics, using optical and magnetic tweezers and single-molecule fluorescence to study DNA/RNA folding, molecular motors, and signal transduction -- one of the earliest applications of AMO-derived single-particle measurement precision to living systems.

Cohen's lab develops genetically encoded fluorescent voltage indicators and all-optical electrophysiology ('Optopatch') to simultaneously stimulate and image membrane voltage in individual neurons and cardiomyocytes at the single-cell and network level, combining protein engineering, optics, and theory to push the temporal and spatial resolution of bioelectrical imaging well past conventional patch-clamp limits.

Curmi is a structural and single-molecule biophysicist whose most-cited work is on the light-harvesting antenna proteins of cryptophyte algae, where he and collaborators reported long-lived electronic coherence at ambient temperature — one of the founding results of the quantum-biology field and still one of its most argued-over. His group determines the structures of these antenna complexes and engineers them, and separately works on protein-based molecular motors and on single-molecule fluorescence and FRET measurements of conformational dynamics. 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 — Curmi supplies the biological systems in which quantum coherence is actually claimed to matter; a pT/sqrt(Hz)-class spin sensor capable of watching radical-pair or exciton dynamics in situ would be aimed at exactly the questions his structures raise. Preferred attribute present: genuine quantum-biology substrate rather than a quantum-flavoured metaphor.

Dhiman holds the professorship for Physical Chemistry of Supramolecular Systems at JGU and is affiliated with the Max Planck Graduate Center. Her group uses single-molecule and super-resolution fluorescence microscopy (SMLM/PAINT-type methods) to watch synthetic supramolecular polymers assemble, exchange monomers and age in real time -- i.e. applying the biological super-resolution toolkit to non-biological self-assembling matter, and toward bioinspired/adaptive systems that behave like living materials. Relative to the established NV-ensemble quantum-sensing playbook (DEER, nanoscale NMR, T1 relaxometry at pT/sqrt(Hz) ensemble sensitivity), this is a technique-driven inclusion: the emphasis is squarely on pushing spatial and temporal resolution of dye-based imaging past the ensemble limit, and it is a newer group where a postdoc would have room to shape the direction.

Gambin was the first EMBL Australia group leader appointed to Single Molecule Science. His signature method combines cell-free protein expression with two-colour single-molecule coincidence and fluctuation spectroscopy, which sidesteps purification entirely: proteins are expressed, labelled and measured in lysate, an order of magnitude faster than conventional interaction assays. The biology is protein self-association and aggregation — alpha-synuclein in Parkinson's, cardiac and muscular disease proteins — where the size distribution of oligomers, not the mean, is the quantity of interest. 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 conceptual overlap with quantum biosensing is the insistence on distributions over averages, and his aggregation systems (paramagnetic-species-generating, redox-active amyloid) are a plausible target for T1-relaxometry-based NV detection at pT/sqrt(Hz) in the near term.