Bain develops advanced laser spectroscopy and super-resolution microscopy techniques for biological applications. Research directions: (1) Femtosecond time-resolved STED (stimulated emission depletion) — combining sub-diffraction spatial resolution with picosecond time resolution to study FRET dynamics in live cells with both spatial and lifetime precision; (2) Time-resolved polarized fluorescence — probing orientation distributions and rotational dynamics of fluorophores; (3) CW STED fluorescence lifetime reconstruction — lower-photodose STED for longer live-cell imaging; (4) Single-molecule FRET to study protein-protein interactions; (5) Single-particle tracking of membrane receptors relevant to viral entry and cancer signaling. Former PhD students include Siân Culley (now King's College, SMLM).
Emmanuel Beaurepaire (DR1 CNRS, LOB/École Polytechnique) is a pioneer of multiphoton and harmonic generation deep-tissue microscopy. Research: (1) two-photon excited fluorescence (2PEF) and three-photon deep-tissue brain imaging; (2) second-harmonic generation (SHG) and third-harmonic generation (THG) label-free imaging of collagen, myosin, myelin; (3) multimodal 3-photon light-sheet microscopy with ultrafast lasers; (4) metabolic imaging using FLIM/NADH. Key LOB permanent staff (May 2024). Active collaboration with LCF/Lasers group on ultrafast laser development.
Bohndiek's VISION Lab, run jointly between the Cavendish Laboratory and the Cancer Research UK Cambridge Institute, develops low-cost optical and photoacoustic imaging technologies to study the tumour microenvironment and vasculature, with a strong translational focus on early cancer detection (e.g. hyperspectral endoscopy for oesophageal cancer). The lab is part of a large interdisciplinary team and regularly recruits postdoctoral researchers.
Develops second- and third-harmonic generation (SHG/THG) nonlinear optical microscopy to image collagen and other non-centrosymmetric structural proteins label-free in tissue, with applications to cancer diagnosis and fibrosis, pushing spatial/orientational resolution of structural imaging in intact tissue.
Jean Dalibard's BEC group at LKB studies quantum gases, BEC, and strongly correlated quantum systems. Research: (1) 2D Bose gases and Berezinskii-Kosterlitz-Thouless transition; (2) gauge fields for neutral atoms — synthetic magnetism; (3) quantum simulation with ultracold atoms. Dalibard is a foundational figure in cold-atom physics; his group at LKB/Collège de France is relevant through quantum gas experiments tied to quantum simulation and precision measurement. Borderline case included given BEC foundations for sensing.
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.
Dunsby co-invented oblique plane microscopy (a single-objective light-sheet technique) and develops multidimensional fluorescence lifetime and light-sheet imaging instrumentation for live-cell and tissue imaging, applied to cancer diagnostics and cell biology.
French is Professor and former Head of the Photonics Group (2001–2013). His group at Imperial (with Dunsby and Neil) develops multidimensional fluorescence imaging technology for life sciences and clinical applications. Research portfolio: (1) FLIM — wide-field time-gated FLIM using gated optical intensifiers and TCSPC for single-cell FRET-based biosensing of protein-protein interactions, cell signalling (kinase activity), and drug-target engagement in multi-well plates; (2) Super-resolved microscopy — STED, easySTORM (lower-cost STORM), and SIM+FLIM for mapping molecular function to biological nanostructure below the diffraction limit; (3) FLIM endoscopy — flexible wide-field FLIM endoscopes for label-free cancer diagnostics (autofluorescence lifetime) and osteoarthritis cartilage; (4) Open-source imaging — automated multiwell plate FLIM reader for high-content drug screening. Satellite lab at Francis Crick Institute.
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.
Hinde is a fluorescence-fluctuation physicist embedded in cell biology: she uses pair-correlation function analysis, number-and-brightness, phasor-FLIM and FRET to read out chromatin compaction, protein-chromatin binding dynamics and nucleocytoplasmic transport in living nuclei, at spatial and temporal scales that conventional imaging averages away. The programme is a technique-pushing one — the emphasis is on extracting nanoscale structural information from photon statistics rather than on brute-force localisation — and it is now being coupled to quantum sensing through her QUBIC investigatorship, where the goal is to combine fluorescence readouts with NV-based magnetic and spin-noise contrast in the same cell. 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 — her role in QUBIC is to supply the cell-biological questions and the correlative optical readouts that make pT/sqrt(Hz)-class ensemble sensing biologically interpretable. Preferred attribute present: lifetime- and orientation-resolved methods pushing past the usual resolution limits.