Defining the proteolytic landscape during enterovirus infection.

Viruses cleave cellular proteins to remodel the host proteome. The study of these cleavages has revealed mechanisms of immune evasion, resource exploitation, and pathogenesis. However, the full extent of virus-induced proteolysis in infected cells is unknown, mainly because until recently the technology for a global view of proteolysis within cells was lacking. Here, we report the first comprehensive catalog of proteins cleaved upon enterovirus infection and identify the sites within proteins where the cleavages occur. We employed multiple strategies to confirm protein cleavages and assigned them to one of the two enteroviral proteases. Detailed characterization of one substrate, LSM14A, a p body protein with a role in antiviral immunity, showed that cleavage of this protein disrupts its antiviral function. This study yields a new depth of information about the host interface with a group of viruses that are both important biological tools and significant agents of disease

Report (U.S. Atomic Energy Commission)

Unit developed at Knolls Atomic Power Laboratory for extraction and overcomes the disadvantages of the batch countercurrent units currently in use

THE 1A HYBRID FLOWSHEET

A preliminary hybrid 1A flowsheet in which the extraction section operates substantially acid while the scrub section is acid deficient is presented. The effects of added nitric acid on the performance of the acid deficient 1A flowsheet are considered, and the need for control of the entering stream acidities in such flowsheets is evaluated. Data on batch-countercurrent decontamination and plutonium recovery are included. (J.R.D.

The 1A Hybrid Flowsheet

A preliminary hybrid 1A flowsheet in which the extraction section operates substantially acid while the scrub section is acid deficient is presented. The effects of added nitric acid on the performance of the acid deficient 1A flowsheet are considered, and the need for control of the entering stream acidities in such flowsheets is evaluated. Data on batch-countercurrent decontamination and plutonium recovery are included. (J.R.D.

Global analysis of posttranslational protein arginylation.

Posttranslational arginylation is critical for embryogenesis, cardiovascular development, and angiogenesis, but its molecular effects and the identity of proteins arginylated in vivo are largely unknown. Here we report a global analysis of this modification on the protein level and identification of 43 proteins arginylated in vivo on highly specific sites. Our data demonstrate that unlike previously believed, arginylation can occur on any N-terminally exposed residue likely defined by a structural recognition motif on the protein surface, and that it preferentially affects a number of physiological systems, including cytoskeleton and primary metabolic pathways. The results of our study suggest that protein arginylation is a general mechanism for regulation of protein structure and function and outline the potential role of protein arginylation in cell metabolism and embryonic development

Novel cell types and developmental lineages revealed by single-cell RNA-seq analysis of the mouse crista ampullaris

This study provides transcriptomic characterization of the cells of the crista ampullaris, sensory structures at the base of the semicircular canals that are critical for vestibular function. We performed single-cell RNA-seq on ampullae microdissected from E16, E18, P3, and P7 mice. Cluster analysis identified the hair cells, support cells and glia of the crista as well as dark cells and other nonsensory epithelial cells of the ampulla, mesenchymal cells, vascular cells, macrophages, and melanocytes. Cluster-specific expression of genes predicted their spatially restricted domains of gene expression in the crista and ampulla. Analysis of cellular proportions across developmental time showed dynamics in cellular composition. The new cell types revealed by single-cell RNA-seq could be important for understanding crista function and the markers identified in this study will enable the examination of their dynamics during development and disease