James E. Evans

The paper determines the near-atomic structure of the P-SSP7 virion and identifies five rotational registers defining modular portal-capsid assembly.

The paper develops a 4D whole-cell model of Prochlorococcus marinus MED4 to show how spatial organization and redox PTMs regulate carbon fixation under light disturbance.

This paper introduces a 5-beam c-SIM technique that improves optical sectioning and lateral resolution in non-fluorescent samples by suppressing coherent defocus effects.

The paper uses visual proteomics to identify functional spirosomes in Clostridium thermocellum during biomass degradation.

The paper shows that anionic fluorescent dyes up to 1 kDa pass through plasmodesmata while smaller cationic ones do not, suggesting plasmodesmal pores may have positive charges.

The paper integrates AMGs and phage assembly into a genome-scale metabolic model to predict their impact on host metabolism and phage production, revealing synergistic and antagonistic effects.

This study improves virus visualization in soil using a simple spin filtration method combined with cryo-electron microscopy, revealing previously unseen morphotypes.

This paper develops a scalable and high-quality method for producing marine cyanophage P-SSP7, enabling efficient structural studies and reducing cryo-EM data collection time.

This paper demonstrates cryo-EM can solve protein structures directly from cell-free expression mixtures with minimal purification, reducing time and reagent use.

This study investigates how cyanobacteria and Chloroflexota cooperate in forming microbial mats through motility and biofilm formation.

This paper expresses and characterizes family-2 glycosyltransferases using a cell-free system, showing their catalytic activity and kinetic properties.

The paper investigates the tunable hetero-assembly of a plant pseudoenzyme-enzyme complex, revealing variable stoichiometry and structural insights into their interactions.

This study expresses and purifies full-length InaZ, an ice nucleating protein, using a wheat-germ cell-free system and confirms its functionality and structural organization as fibrils.

This paper demonstrates a wheat-germ cell-free protein expression pipeline that generates high-purity proteins for structural biology analysis.

The paper uses multimodal imaging and multi-omics techniques to study O. tauri's cellular responses to nitrogen and carbon ratio changes, revealing shifts in lipid and starch metabolism.

This study optimizes growth conditions for Ostreococcus tauri in a photobioreactor, achieving 4-times faster growth and 10-fold higher biomass.

The study identifies Ostreococcus tauri as an oleaginous green alga with unique lipid droplet secretion mechanisms resembling pea-pod structures.