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Biology subjects

Chan, F. Y.

Publications and source records attributed to Chan, F. Y..

2 recordsLinked to original sources

A look beyond topography: transient phenomena of Escherichia coli cell division captured with high-speed in-line force mapping

Life on the nanoscale has been made accessible in recent decades by the development of techniques that are fast and non-invasive. High-speed atomic force microscopy (HS-AFM) is one such technique that has proven to shed light on elusive mechanisms involving single proteins. Extending HS-AFM to effortlessly incorporate mechanical property mapping while maintaining fast imaging speed allows us to look deeper than topography and reveal more details of the nanoscale mechanisms that govern life. Here, we present high-speed in-line force mapping (HS-iFM), which enables the recording of mechanical properties and topography maps with high spatiotemporal resolution. Employing this method, a detailed study of the dynamic nanoscale mechanical properties of living Escherichia coli bacteria reveals localized stiffening during division, intricate details of the division process, formation and diffusion of pores in the membrane, and the impact of depressurization of a cell. All of these phenomena were recorded with a frame time as low as 15 s and a spatial resolution of 5.5 nm/pixel in topography and 22 nm/pixel in force maps, allowing the capture of transient phenomena on bacterial surfaces in striking detail.

biophysics↗

Flow-independent accumulation of motor-competent non-muscle myosin II in the contractile ring is essential for cytokinesis

Cytokinesis in animal cells requires the assembly of a contractile actomyosin ring, whose subsequent constriction physically separates the two daughter cells. Non-muscle myosin II (myosin) is essential for cytokinesis, but the role of its motor activity remains poorly defined. Here, we examine cytokinesis in C. elegans one-cell embryos expressing myosin motor mutants generated by genome editing. Motor-dead myosin, which is capable of binding F-actin, does not support cytokinesis, and embryos co-expressing motor-dead and wild-type myosin are delayed in cytokinesis. Partially motor-impaired myosin also delays cytokinesis and renders contractile rings more sensitive to reduced myosin levels. Thus, myosin motor activity, rather than its ability to cross-link actin filaments, drives contractile ring assembly and constriction. We further demonstrate that myosin motor activity is required for long-range cortical actin flows, but that flows per se play a minor role in contractile ring assembly. Our results suggest that flow-independent recruitment of motor-competent myosin to the cell equator is both essential and rate-limiting for cytokinesis.

cell biology↗