Research Areas - (214) Biophysics

Full path: Biology > Biophysics

Department(s)/lab(s): BioNanoscience / Kavli Institute of Nanoscience | Arjen Jakobi Lab — Cryo-EM Structural Cell Biology @ TU Delft
Summary:

Arjen Jakobi (Associate Professor, BioNanoscience) uses cryo-electron microscopy and tomography for structural cell biology. Research: (1) cryo-ET in-cell structural biology — resolving protein complexes at near-atomic resolution inside vitrified cells; (2) autophagy and membrane remodelling — structural mechanism of autophagosome biogenesis; (3) integrin signalling complexes. Develops algorithms for sub-tomogram averaging and de-novo model building.

Department(s)/lab(s): Biological Engineering | Jasanoff Lab @ MIT
Summary:

PREFERRED. Jasanoff's lab develops genetically encoded and nanoparticle/small-molecule MRI sensors (for calcium, dopamine, serotonin, and other neurochemical targets) that convert molecular binding events into brain-wide, noninvasive MRI contrast changes, effectively giving whole-brain 'molecular fMRI' with a growing palette of chemically distinct reporters; recent work includes liposomal nanoprobes actuated by engineered water channels for higher-sensitivity detection.

Department(s)/lab(s): Physics & Astronomy – Biophysics | Jones Lab (Optical Tweezers Biophysics) @ UCL
Summary:

Jones's group develops optical tweezers instrumentation for biological applications. Research directions: (1) Single-cell mechanics — using optical traps to apply calibrated forces to cells and measure viscoelastic properties relevant to cancer invasion and immune response; (2) Motor protein biophysics — measuring force-velocity curves of kinesin/myosin motors at the single-molecule level; (3) Optical sorting — holographic optical tweezers for cell sorting by mechanical phenotype; (4) Instrument development — fast-switching AOD-based traps, quantitative phase imaging combined with force measurement. Sensitive to pN forces, combining biosensing with fundamental biophysics.

Department(s)/lab(s): BioNanoscience / Kavli Institute of Nanoscience | Chirlmin Joo Lab — Single-Molecule RNA and CRISPR @ TU Delft
Summary:

Chirlmin Joo (Full Professor, BioNanoscience) uses single-molecule fluorescence to study RNA dynamics and CRISPR-Cas. Research: (1) single-molecule FRET and direct RNA imaging — visualizing RNA folding, ribozyme catalysis, and mRNA translation dynamics; (2) CRISPR-Cas mechanism — real-time observation of Cas9 and Cas13 target search and cleavage; (3) nanopore-based protein sensing integration with optical tools. ERC Grant.

Department(s)/lab(s): Imaging Physics (ImPhys) | Kalkman Lab (OCT Spectroscopy) @ TU Delft
Summary:

Jeroen Kalkman develops optical tomography and spectroscopy methods for biomedical imaging. Research: (1) Fourier-domain OCT including spectroscopic OCT for tissue structural and functional imaging; (2) novel light sources and detectors for skin cancer detection (NWO KIC project NextDeLights); (3) scattering media imaging. His work is relevant to advanced biosensing with optical coherence.

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Department(s)/lab(s): Chemical Engineering and Biotechnology | Laser Analytics Group @ Cambridge
Summary:

Kaminski's Laser Analytics Group develops laser-based super-resolution and fluorescence-lifetime imaging methods (STED, SIM, dSTORM, FLIM) and applies them, with long-time collaborator Gabriele Kaminski Schierle, to visualise amyloid protein aggregation in live cells and organisms as a route to understanding neurodegenerative disease; the group also directs the EPSRC Centre for Doctoral Training in Sensor Technologies.

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Department(s)/lab(s): Chemical Engineering and Biotechnology | Molecular Neuroscience Group @ Cambridge
Summary:

Kaminski Schierle heads the Molecular Neuroscience Group, applying super-resolution and functional fluorescence imaging (developed with Clemens Kaminski) to gain molecular-level understanding of protein misfolding in Alzheimer's, Parkinson's and Huntington's disease models, including live-cell and whole-organism (C. elegans) imaging of amyloid aggregation.

Department(s)/lab(s): Physics (Biological Physics, Condensed Matter Physics) | Gene Machines (Kapanidis Group) @ Oxford
Summary:

Kapanidis' Gene Machines group develops single-molecule fluorescence methods (including ALEX/FRET and super-resolution microscopy) to observe transcription and other gene-expression machinery in real time in bacteria and viruses, and leverages this toolkit to build ultrasensitive DNA-based biosensors for pathogen and antibiotic-resistance detection.

Department(s)/lab(s): School of Chemistry | Kassal Group @ USyd
Summary:

Kassal is the leading Australian theorist of quantum effects in light harvesting. He established the distinction between coherent processes and coherent states in photosynthesis — showing that under incoherent sunlight at steady state, wavelike motion per se does not enhance efficiency, while environment-assisted transport and supertransfer genuinely can — and has since developed a classification of the mechanisms by which coherence (excitonic, vibrational, or of the light field itself) can improve energy transport. He also pioneered quantum-computer algorithms for chemistry. A distinct and directly relevant thread is the theory of spectroscopy with non-classical light: what entangled or squeezed photons can reveal about molecular coherence that classical light cannot. 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 work is the theoretical counterpart to the quantum-biology ambitions of the NV community: where NV ensembles at pT/sqrt(Hz) try to detect the magnetic signatures of biological spin chemistry, Kassal asks what quantum coherence is actually doing in those systems and whether quantum light can interrogate it.

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Department(s)/lab(s): Neurobiology | Kasthuri Lab @ UChicago
Summary:

Kasthuri pioneered automated large-volume serial electron microscopy ('connectomics') to reconstruct complete synaptic wiring diagrams of the brain, and is now exploring synchrotron X-ray and photoemission electron microscopy (with the King lab) to remove imaging-speed bottlenecks and scale reconstructions toward whole-mouse and eventually human brains, comparing development, aging, and species differences. This is squarely the kind of resolution-pushing biological imaging the filter targets, achieving nanometer-scale synaptic resolution across cubic-millimeter-to-whole-brain volumes.