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Zagoriy, E.

Publications and source records attributed to Zagoriy, E..

2 recordsLinked to original sources

Structural reorganization underlying stress-induced cytoplasmicsolidification in yeast

Cells employ diverse strategies to rapidly adapt to sudden environmental changes. In yeast, cytoprotective solidification in response to starvation and energy depletion (ED) has been reported and associated with extensive mesoscale macromolecular assembly. Yet, the structural and molecular basis underlying such whole-cell level liquid-to-solid phase transitions remain unknown. Here, we use cryo-electron tomography to characterize the subcellular organization of intact yeast cells exposed to ED and other stressors, and to untangle the effects of molecular crowding versus cytoplasmic acidification previously suggested to underpin solidification. We visualize self-assembly of macromolecules and complexes into ordered assemblies and condensates under ED, and quantify ribosome and polysomes concentrations to probe changes in cytoplasmic crowding. Combined with live-cell microscopy, we pinpoint supramolecular assembly induced by acidification, rather than a uniform increase in intracellular crowding, as the structural basis of cytoplasmic solidification that supports yeast cells adaptation in response to environmental stresses.

molecular biology↗

Native molecular architectures of centrosomes in C. elegans embryos

Centrosomes organize microtubules that are essential for mitotic divisions in animal cells. They consist of centrioles surrounded by Pericentriolar Material (PCM). Questions related to mechanisms of centriole assembly, PCM organization, and microtubule formation remain unanswered, in part due to limited availability of molecular-resolution structural analyses in situ. Here, we use cryo-electron tomography to visualize centrosomes across the cell cycle in cells isolated from C. elegans embryos. We describe a pseudo-timeline of centriole assembly and identify distinct structural features including a cartwheel in daughter centrioles, and incomplete microtubule doublets surrounded by a star-shaped density in mother centrioles. We find that centriole and PCM microtubules differ in protofilament number (13 versus 11) indicating distinct nucleation mechanisms. This difference could be explained by atypical {gamma}-tubulin ring complexes with 11-fold symmetry identified at the minus ends of short PCM microtubules. We further characterize a porous and disordered network that forms the interconnected PCM. Thus, our work builds a three-dimensional structural atlas that helps explain how centrosomes assemble, grow, and achieve function.

cell biology↗