Every minute, cells make millions of new proteins which must be transported to the correct location, folded, modified and assembled with other proteins in order to function properly. Failure at any of these maturation steps can reduce protein function and lead to the accumulation of aberrant protein intermediates, resulting in disease.
Uncovering the molecular basis of triage during protein synthesis
IL-17, a regulator of the immune system, impacts behaviour
The state of the immune system has effects on brain function, but despite suggestions that immunoregulators can affect people’s mood and behaviour, we are only beginning to understand how these two major body systems interact. The contributions of a neuron to circuit activity and behaviour depend on its responsiveness to upstream inputs, and its ability to drive downstream outputs.
New insights into the structure and dynamics 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. Research by Kiyoshi Nagai’s group in the LMB’s Structural Studies Division, has previously revealed the structure of the spliceosome in a fully active, substrate-bound state, immediately after its first catalytic reaction. The group has now expanded upon this work revealing the near-atomic level structure of the spliceosome just before mRNA formation.
New hypothesis for the formation of macropinocytic cups
Macropinocytosis, the cellular uptake of fluids from the environment, is employed by a variety of cells and requires the formation of a cup-shaped structure that protrudes from the cell’s surface and captures gulps of medium. Polymerisation of actin under the plasma membrane drives the extension of macropinocytic cups. However, until now it has been unclear how the actin forming the walls of the cup is shaped into a ring.
Recovering stalled ribosomes
Ribosomes are cellular molecular machines that link amino acids together in the order specified by messenger RNA (mRNA) to make proteins. Near the end of the mRNA molecule a specific nucleotide sequence, known as a stop codon, signals for protein synthesis to terminate by recruiting release factors that release the newly made protein from the ribosome and recycle the ribosome to start another round of protein synthesis.
However, some mRNA molecules are defective.
New technologies enable systematic recoding of genomes
The design and synthesis of genomes provides a powerful approach for understanding and engineering biology. The development of methods that can accurately replace the genome in sections, provide feedback on precisely where a given design fails and on how to repair it, and that can be rapidly repeated for whole genome replacement would accelerate our ability to understand and manipulate the information encoded in genomes. Using E.