Each year scientists pair up with UK parliamentarians to gain an insight into each other’s worlds, as part of the Royal Society’s Parliamentary Pairing Scheme. Glenn Masson, a postdoc from the MRC Laboratory of Molecular Biology in Cambridge, shares his experience of welcoming an MP into his lab.
Daniel Zeichner, MP for Cambridge, arrived on my doorstep at midday. My lab doorstep that is, at the MRC Laboratory of Molecular Biology (LMB). He was here to shadow my day and see what we researchers spend our days doing with public funding.
Image credit: MRC Laboratory of Molecular Biology
My week in Parliament – the first leg of our exchange – exposed me to the breadth of MP’s interests. As we briskly made our way around Westminster, national and European headlines ran alongside constituents’ concerns; Daniel’s attention was dragged from one issue to the next at an unrelenting pace.
This image has been created by a team at the MRC Laboratory of Molecular Biology (MRC LMB) in collaboration with the University of Exeter and Birkbeck College and, for the first time, shows a detailed structure of a ‘lysenin pore’. Dr Christos Savva, an Electron Microscopy Facility scientist at the MRC LMB spoke to Sylvie Kruiniger about why understanding these structures could be the key to treating many different diseases.
It may look like some kind of technicolour mushroom but this teeny structure is actually a cell-attacking pore made of just nine proteins.
Sir John Sulston is best known for the leading role he played in the Human Genome Project. But earlier in his career, he studied the development of the nematode worm. Sarah Harrop tells the story behind a lab notebook entry which contributed to a Nobel Prize-winning breakthrough.
A page from John Sulston’s 1980 lab notebook showing his cell-tracking method (Image: Wellcome Images under CC BY 4.0)
These intricate biro scribblings are from the 1980 lab notebook of Sir John Sulston, completed when he was a young postdoc at the MRC Laboratory of Molecular Biology (LMB) in Cambridge. They’re the result of hours spent staring at the embryos of nematode worms under the microscope, hand-drawing their tiny cells as they divided.
Early 1980s technology wasn’t up to photographing the cells at a high enough resolution to see them dividing. So John took on the ambitious task of watching and recording each and every cell division of the developing embryo to trace the origin of each cell. Read more