HIV is a retrovirus, meaning it has to copy its RNA genome into DNA in order to infect cells. While much has been learned about the virus, investigators don’t understand how it evades our immune system so successfully. A long-standing question has been how the HIV virus copies its genome using raw materials from the cell without being detected by immune sensors.
HIV uses capsid pores to import nucleotides and evade innate immunity
An evolutionarily conserved pathway controls proteasome homeostasis
Cell survival depends on adaptive signalling pathways to ensure that the supply of vital components matches the fluctuating needs of the cell. The proteasome is essential for the selective degradation of most cellular proteins and thereby controls virtually all cellular processes. The current prevailing view is that protein degradation is largely regulated at the level of ubiquitination.
Structure of the catalytic spliceosome
The spliceosome is a molecular machine, which together with RNA polymerases and ribosomes plays a critical role in basic gene expression. Due to its highly dynamic nature the structure of the spliceosome has remained elusive until now. Research by Kiyoshi Nagai’s group, in the LMB’s Structural Studies Division, has for the first time captured the spliceosome in a fully active, substrate-bound state, immediately after first catalytic reaction.
NBLAST – a new online tool to compare neurons
Researchers in Greg Jefferis’s group in the LMB’s Neurobiology Division have developed a new online tool to analyse images of neurons. This tool, known as NBLAST, is free and available to all. NBLAST enables researchers to measure the similarity between neurons and organise them into neuron families, akin to tools such as BLAST that allow protein sequences to be compared.
Neuroscience is seeing a period of major growth in the structural characterisation of neurons.
In vivo visualisation and quantification of the circadian clock protein Period2
Circadian clocks are found across all higher species, controlling daily rhythms of behaviour and physiology. They are thought to “tick” by producing and then degrading circadian proteins on a 24 hour cycle. At a molecular level, they typically involve expression of “clock” genes that are inhibited approximately every 24 hours by the proteins they encode.
A protein quality control system for mislocalised proteins
In order to function properly, many of the cell’s proteins need to be segregated to membrane-bound organelles and assembled into multi-protein complexes. Newly made proteins that fail to be localised or assembled properly must be promptly recognised by the cell and destroyed. These pathways of protein quality control are important because the accumulation of aberrant proteins can lead to neurodegeneration and various other diseases.