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BiophysTO Lunchtime Talks Past Events /

01 - 03
May 2020
8:15 a.m. - 8:15 p.m.
TBA
Chemical Biophysics Symposium
The Chemical Biophysics Symposium (CBP) is a student-organized conference, which provides an informal venue for discussions on some of the most intriguing topics at the interface of chemistry, biology, and physics.
06
Apr 2017
noon - 1 p.m.
St. George, MP606
Dr. Oliver Ernst
TBA
23
Mar 2017
4 p.m. - 5 p.m.
St. George, MP102
Dr. Cristina Marchetti
TBA
09
Mar 2017
noon - 1 p.m.
St. George, MP606
Dr. Kandice Tanner
Probing the biophysical regulation of the de novo tumor microenvironment
23
Feb 2017
noon - 1 p.m.
St. George, MP606
Dr. Roman Melnyk
How Bacterial Toxins Deliver Proteins Across Membranes and into Cells
Protein translocases, found in all kingdoms of life, facilitate the transport of proteins across biological membranes. How these membrane-embedded translocases recognize and transport their heterogeneous and structurally unwieldy protein substrates across membranes is poorly understood.
09
Feb 2017
noon - 1 p.m.
St. George, MP606
Dr. Gregoire Altan-Bonnet
Single-cell modeling of the dysfunctional signaling in Chronic Lymphocytic Leukemia
Novel methods in biological physics are becoming critical in clinical application, to functionally interpret cancer genomic alterations. For Chronic Lymphocytic Leukemia (CLL), a heterogeneous disease of B-lymphocytes maturing under constitutive B-cell receptor (BCR) stimulation, the functional role of diverse clonal mutations remains largely unknown. We present here a combination of single-cell measurements and computational modeling to demonstrate that alterations in BCR signaling dynamics underlie the progression of B-cells toward malignancy. We apply nonlinear dynamics methods to reveal emergent dynamic features, namely bimodality, hypersensitivity, and hysteresis, in the BCR signaling pathway of primary CLL B-cells. We demonstrate that such signaling abnormalities in CLL quantitatively derive from BCR clustering and constitutive signaling with positive feedback reinforcement, as demonstrated through single-cell analysis of signaling motifs, computational modeling, and superresolution imaging. Such dysregulated signaling segregates CLL patients by disease severity and clinical presentation. Our findings provide a novel quantitative framework and illustrate how approaches borrowed from biological physics help assess complex and heterogeneous cancer pathology.
26
Jan 2017
noon - 1 p.m.
St. George, MP606
Dr. Sevan Hopyan
TBA
12
Jan 2017
noon - 1 p.m.
St. George, MP606
Dr. Tony Harris
TBA
08
Dec 2016
4 p.m. - 5 p.m.
St. George, MP102
Dr. Massimo Vergassola
TBA
01
Dec 2016
noon - 1 p.m.
UTM (streamed to MP606)
Dr. Guillaume Salbreux
Physics of Tissue Morphogenesis: from cellular forces to tissue shape
17
Nov 2016
noon - 1 p.m.
MP606
Dr. Carlos Ramos
Studies on structure, function and interactions of the heat shock protein Hsp40
03
Nov 2016
noon - 1 p.m.
St. George, MP606
Dr. Will Navarre
How bacterial gene silencing proteins contribute to the evolution of pathogens
20
Oct 2016
noon - 1 p.m.
UTM
Dr. Kari Dalnoki-Veress
TBA
06
Oct 2016
noon - 1 p.m.
St. George, MP606
Dr. Gil Prive
Protein-lipid complexes in the lysosome
22
Sep 2016
noon - 1 p.m.
St. George, MP606
Dr. Simon Sharpe
TBA
08
Sep 2016
noon - 1 p.m.
St. George, MP606
Dr. Patrick Barth
Reprogramming membrane protein function by design
21
Apr 2016
noon - 1 p.m.
TBA
Dr. Jonathon Rocheleau
The design and application of genetically encoded Apollo-NADP+ sensors to image cellular metabolism in tissues
07
Apr 2016
noon - 1 p.m.
Davenport Room, Chemistry Building
Dr. Craig Peterson
Chromatin Remodeling Machines
24
Mar 2016
noon - 1 p.m.
TBA
Dr. Nelly Pante
How viruses cross the gate much traveled: Transport of viruses into the cell nucleus
10
Mar 2016
noon - 1 p.m.
UTM, Davis Building 3129
Dr. Elizabeth Rhoades
Order from disorder - defining structure in disordered proteins
In contrast to globular proteins, intrinsically disordered proteins do not form stable, compact structures under physiological conditions. Rather, often their functions are derived from their properties as extended, flexible polymers.
25
Feb 2016
midnight - 1 p.m.
TBA
Dr. Hue Sun Chan
How Does an Enzyme Unknot DNA? Statistical Mechanics of Disentangling by Topoisomerases
11
Feb 2016
midnight - 1 p.m.
Davenport Room, Chemistry Building
Dr. Chris Yip
New Initiatives in Combinatorial Microscopies: From Single Molecules to Developmental Events
28
Jan 2016
midnight - 1 p.m.
TBA
Dr. Chris Bergevin
The Active Ear
The ear is a remarkable detector: It is both highly sensitive and selective, and operates over a large dynamic range spanning more than 12 orders of magnitude. Not only does it respond to sound, but emits it as well. These sounds, known as otoacoustic emissions (OAEs), provide a means to probe the fundamental biophysics underlying transduction and amplification in the ear. This talk will describe the empirical nature of OAE data, as well as theoretical approaches describing the underlying biomechanics using coupled oscillators. While this modeling focuses on the auditory system, an underlying goal is to identify emergent behavior (e.g., phase coherence) that arises universally in qualitatively similar complex biological systems (e.g., neural networks).
14
Jan 2016
midnight - 1 p.m.
Davenport Room, 3rd Floor, 80 St. George Street
Dr. Ran Kafri
Hearing the shape of life: mathematical explorations of cell biology.
Hidden inside of a single individual living cell there exists a dynamical system of multiple, interrelated, chemical processes. Collectively, it is these dynamics and chemical interrelations that define life.
17
Dec 2015
noon - 1 p.m.
Davenport Room, 3rd Floor, 80 St. George Street
Dr. Walid Houry
Formation of an amyloid state by a bacterial protein: structure and consequences

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