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Biology subjects

Genthial, R.

Publications and source records attributed to Genthial, R..

2 recordsLinked to original sources

A spectral demixing method for high-precision multi-color localization microscopy

Single molecule localization microscopy (SMLM) with a dichroic image splitter can provide invaluable multi-color information regarding colocalization of individual molecules, but it often suffers from technical limitations. So far, demixing algorithms give suboptimal results in terms of localization precision and correction of chromatic aberrations. Here we present an image splitter based multi-color SMLM method (splitSMLM) that offers much improved localization precision & drift correction, compensation of chromatic aberrations, and optimized performance of fluorophores in a specific buffer to equalize their reactivation rates for simultaneous imaging. A novel spectral demixing algorithm, SplitViSu, fully preserves localization precision with essentially no data loss and corrects chromatic aberrations at the nanometer scale. Multi-color performance is further improved by using optimized fluorophore and filter combinations. Applied to three-color imaging of the nuclear pore complex (NPC), this method provides a refined positioning of the individual NPC proteins and reveals that Pom121 clusters act as NPC deposition loci, hence illustrating strength and general applicability of the method.

biophysics↗

Spindle alignment is uncoupled with Kar9 symmetry breaking

Spindle positioning must be tightly regulated to ensure asymmetric cell divisions are successful. In budding yeast, spindle positioning is mediated by the asymmetric localization of microtubule +end tracking protein Kar9. Kar9 asymmetry is believed to be essential for spindle alignment. However, the temporal correlation between symmetry breaking and spindle alignment has not been measured. Here, we establish a method of quantifying Kar9 symmetry breaking and find that Kar9 asymmetry is not well coupled with early spindle alignment. We report the majority of asymmetric cells are not stably aligned. Rather, stable alignment, a state we define as perfect alignment, is correlated with Kar9 localization to the bud compartment, regardless of symmetry state. Our findings suggest that Kar9 asymmetry alone is insufficient for perfect alignment and reveal a possible role for Swe1 in regulating spindle alignment efficiency.

cell biology↗