Seminars

Gašper Tkačik explores whether the language of information in biology can become a predictive scientific theory. The lecture connects information transfer from DNA to proteins, positional signals that guide cell fate during development, neural information processing, and the storage and inheritance of information in evolving genomes. It brings physics, information theory and quantitative biology together to examine these processes across biological scales. Tkačik is Professor at the Institute of Science and Technology Austria. Shinya Kuroda provides commentary; Arisa Ema moderates. Online via Zoom Webinar. Wednesday 14 October 2026, 14:00–15:00 JST (Asia/Tokyo; UTC+9). Public advance registration is required through the organizer’s event page. The lecture is in English with Japanese interpretation. Organized by Tokyo College, The University of Tokyo Institutes for Advanced Study.

Ilaria Ferlenghi discusses a career spanning structural biology, cryo-electron microscopy, vaccine research and development, and the growing role of artificial intelligence and machine learning in scientific innovation and entrepreneurship.

Real-time measurement of local biomolecule concentrations in living tissue requires sensors that are stable, selective and minimally invasive. This seminar examines single-walled carbon nanotubes, whose durable near-infrared fluorescence and sensitivity to their surroundings support optical biosensing. Biopolymer functionalization gives the nanotubes biological compatibility and selectivity for particular molecular targets. Spectroscopy, microscopy and machine-learning-assisted analysis are used to characterize sensor interactions and extract biological information, with applications spanning live-cell imaging, wearable sensing and continuous monitoring.

Clarice D. Aiello examines evidence that quantum effects influence biological function, including magnetic sensing used in animal navigation, cellular metabolism and enzyme activity, and the capture of light energy in photosynthesis. The talk reviews proposed biophysical mechanisms and their implications for human, plant and environmental biology, while considering the difficulty of connecting observations from nanometre scales to whole organisms. A central question is whether quantum mechanics can be established or ruled out as the explanation for physiologically relevant effects, and whether those effects can be controlled for useful applications. Potential directions include biomimetic electromagnetic probes, quantum-computing architectures that operate at room temperature, improved solar-energy devices and new therapies. Progress will require work across disciplines and scales, with theory and experiment developed together.

Paul S. Weiss (UCLA) explores low-energy interactions and balanced cycling in natural systems as models for efficient synthetic devices and recycling. Because the relevant energies fall below visible-photon energies, tunnelling spectroscopy and imaging are used to probe these processes. Replicating biochemical cycling and low-energy transport could reduce the energy needed for devices and materials recovery. The work seeks missing physical principles, including spin conservation in chiral molecules and polarizability in biological and synthetic systems. This perspective has led to thermal-control advances in scale, speed and magnitude. Atomic-resolution imaging, spectroscopy and functional measurements help build precise structures while revealing heterogeneous nanoscale behaviour. The talk relates these advances to the physical, electronic, mechanical, thermal and chemical connections between materials and their surroundings that determine future nanomaterial measurements and devices.

How do humans stabilize an inverted pendulum, and why does a balanced pole eventually fall? Drawing on 25 years of fingertip pole-balancing research, this talk examines neural correction delays: longer poles move more slowly relative to the nervous system’s response time. Delay-differential models can stabilize the upright position, yet skilled people still experience falls. The proposed explanation is microchaos arising from interactions among delay, sensory dead zones and frequency-dependent force encoding. A region of transient falling solutions lies next to stable microchaotic dynamics. Such microchaos is absent in virtual frontal-plane balancing tasks, while models of standing postural sway lack the corresponding transient regime. The comparison suggests that human falls, unlike pole falls, are more plausibly associated with medical events or slips and trips.

To orchestrate complex behaviors in mammals, the cerebral cortex must continuously transmit its processing results to subcortical regions. While internal cortical processing relies on highly selective sparse codes, these descending cortical output streams employ an enigmatic dense code, characterized by high firing rates and low feature selectivity. This dense population code presents a profound paradox: how can downstream regions extract precise, cognitively relevant signals when most cortical output neurons can be active at any moment? We address this paradox by testing the hypothesis that cortex does not lose information when switching to a dense code. Instead, it utilizes a mechanism for sparse-to-dense coding transformations discovered by my laboratory: thalamocortical synapses target specifically the dendritic initiation zone for calcium action potentials (APs), which enables cortical output neurons to transmit multiple information streams simultaneously via a multiplexed 1-2-3 AP syntax. I will provide first evidence that this remarkable synaptic specificity and coding syntax generalize across long-range pathways. Information coupling via an anatomically and biophysically distinct dendritic nexus may hence be a ubiquitous mechanism for sparse-to-dense coding transformations in cortex. Dissecting these mechanistic origins of cortical output streams is only now possible due to a unique in vivo – in silico approach, perfected over two decades, that my laboratory developed for bridging the gaps between dendritic and population-level computations

Richard Huang investigates how DNA nanostructures deform under uneven hydrodynamic forces, a question relevant to drug delivery, vaccines and biosensors. Coarse-grained molecular dynamics and mechanical models first examine linear and circular DNA in extensional flow. Drag concentrates tension near the middle of linear duplexes, disrupting base pairs and causing overstretching. Deforming minicircles straighten along their sides while concentrating bending into opposing tips and localized kinks. Models based on DNA elasticity and hydrodynamic-force distributions explain these responses, then extend to wireframe DNA origami to study force transmission and how local structural transitions produce whole-particle deformation. The results inform structures designed for stability or controlled deformation in flow. Online via Zoom. Friday 2 October 2026, 12:00–13:00 EDT (America/New_York; UTC−4). Open the Zoom link on the official event page; the audience explicitly includes the public. Richard Huang is affiliated with MIT. Organized by MIT Department of Mathematics — Computational Research in Boston and Beyond Seminar.

Cryopreservation constrains manufacturing and clinical delivery of immune cells such as NK and T cells. DMSO protects against freezing but becomes toxic at physiological temperatures; associated infusion morbidity can require washing or divided dosing that diminishes therapeutic effectiveness. This talk presents an alternative in which reversible, cytocompatible hydrogels encapsulate cells before freezing without DMSO. The speaker examines evidence that encapsulation cushions osmotic stress, suppresses kinetic and phase transitions, and reduces injury caused by extracellular ice growth and fusion. The discussion covers recovery efficiency, function after thawing, control of biological stress responses, and the challenges of extending the approach to clinical-scale cell preservation.

Mark Harnett presents work on how synaptic organization, nonlinear dendritic processing, and neuronal activity patterns interact to support computation, flexibility, and learning in the adult mammalian neocortex. The Brain and Cognitive Sciences colloquium is followed by a reception.

Thesis presentation by Tiffany Zhang, graduate fellow in the Vinogradova Lab at The Rockefeller University, on chemical proteomics approaches revealing post-translational remodeling of endosomal pathways during macrophage activation. Open to the tri-institutional community.

Klemens Rottner (Helmholtz Centre for Infection Research, Braunschweig) presents evidence that profilin acts as a master regulator of actin filament dynamics essential for cell migration and growth, controlling both formin- and Arp2/3 complex-dependent actin assembly pathways.

Different brain cell types exhibit distinct metabolic signatures that link energy economy to cellular function. Astrocytes and neurons, for instance, diverge dramatically in their reliance on glycolysis versus oxidative phosphorylation, underscoring that metabolic fuel efficiency is not uniform across cell types. A key factor shaping this divergence is the structural organization of the mitochondrial respiratory chain into supercomplexes. Specifically, complexes I (CI) and III (CIII) form a CI–CIII supercomplex, but the degree of this assembly varies by cell type. In neurons, CI is predominantly integrated into supercomplexes, resulting in highly efficient mitochondrial respiration and minimal reactive oxygen species (ROS) generation. Conversely, in astrocytes, a larger fraction of CI remains unassembled, freely existing apart from CIII, leading to reduced respiratory efficiency and elevated mitochondrial ROS production. Despite this apparent inefficiency, astrocytes boast a highly adaptable metabolism capable of responding to diverse stressors. Their looser CI–CIII organization allows for flexible ROS signaling, which activates antioxidant programs via transcription factors like Nrf2. This modular architecture enables astrocytes not only to balance energy production but also to support neuronal health and influence complex organismal behaviors.

Explore how microfluidic chips can enhance your imaging experiments by increasing control, throughput, or flexibility. In this remote, personalized workshop, participants will receive expert guidance, support and chips to run tests on their own microscopes.

Nervous system function relies on the polarized architecture of neurons, established by directional transport of pre- and postsynaptic cargoes. While delivery of postsynaptic components depends on the secretory pathway, the identity of the membrane compartment(s) that supply presynaptic active zone (AZ) and synaptic vesicle (SV) proteins is largely unknown. I will discuss our recent advances in our understanding of how key components of the presynaptic machinery for neurotransmitter release are transported and assembled focussing on our studies in genome-engineered human induced pluripotent stem cell-derived neurons. Specifically, I will focus on the composition and cell biological identity of the axonal transport vesicles that shuttle key components of neurotransmission to nascent synapses and on machinery for axonal transport and its control by signaling lipids. Our studies identify a crucial mechanism mediating the delivery of SV and active zone proteins to developing synapses and reveal connections to neurological disorders. In the second part of my talk, I will discuss how exocytosis and endocytosis are coupled to maintain presynaptic membrane homeostasis. I will present unpublished data regarding the role of membrane tension in the coupling of exocytosis and endocytosis at synapses. We have identified an endocytic BAR domain protein that is capable of sensing alterations in membrane tension caused by the exocytotic fusion of SVs to initiate compensatory endocytosis to restore plasma membrane area. Interference with this mechanism results in defects in the coupling of presynaptic exocytosis and SV recycling at human synapses.

Binary and analog variation of synapses between cortical pyramidal neurons

n the neurosciences the need for some 'overarching' theory is sometimes expressed, but it is not always obvious what is meant by this. One can perhaps agree that in modern science observation and experimentation is normally complemented by 'theory', i.e. the development of theoretical concepts that help guiding and evaluating experiments and measurements. A deeper discussion of 'brain theory' will require the clarification of some further distictions, in particular: theory vs. model and brain research (and its theory) vs. neuroscience. Other questions are: Does a theory require mathematics? Or even differential equations? Today it is often taken for granted that the whole universe including everything in it, for example humans, animals, and plants, can be adequately treated by physics and therefore theoretical physics is the overarching theory. Even if this is the case, it has turned out that in some particular parts of physics (the historical example is thermodynamics) it may be useful to simplify the theory by introducing additional theoretical concepts that can in principle be 'reduced' to more complex descriptions on the 'microscopic' level of basic physical particals and forces. In this sense, brain theory may be regarded as part of theoretical neuroscience, which is inside biophysics and therefore inside physics, or theoretical physics. Still, in neuroscience and brain research, additional concepts are typically used to describe results and help guiding experimentation that are 'outside' physics, beginning with neurons and synapses, names of brain parts and areas, up to concepts like 'learning', 'motivation', 'attention'. Certainly, we do not yet have one theory that includes all these concepts. So 'brain theory' is still in a 'pre-newtonian' state. However, it may still be useful to understand in general the relations between a larger theory and its 'parts', or between microscopic and macroscopic theories, or between theories at different 'levels' of description. This is what I plan to do.