Thursday - gone but still a scientist, SCIENCE!
Your Scientist ID:
Christ King Secondary School, Cork, 1996-2002. UCC 2002-2004. Cork Insitute of Technology 2004-2007. Dublin Institute of Technology, 2008-2011. Dublin City University 2011-present
BSc. Biomedical Science (CIT 2007), BSc. Biomedical Science Hons. (DIT 2011), MSc. Biomedical Diagnostics (DCU 2012)
Science jobs: Hospital, chemistry lab, water testing lab. Weekend jobs: McDonalds, Tesco, Waterstones, New Look, phoneshop
I am a PhD researcher, participating in the BioAT programme
Dublin City University
My Work: I study the sugars on the surface cells and how they change as a cell dies
Every single one of your cells is covered in sugar molecules that can provide clues about how well the cell is doing. In particular I look at a type of blood cell called a lymphocyte, and how its sugar changes as it dies. The type of lymphocyte I am interested in is an important part of your immune system, that produces special proteins that help to destroy invading viruses and bacteria. As these cells die, they lose their outmost sugars, and that lets other cells of the immune system see that they are dying and removes them from our bodies.
My work involves growing these cells in flasks, killing them, and then looking for the changes in the sugars using sugar-binding-proteins and a device called a flow cytometer. The sugar-binding proteins recognise different types of sugars on the cells surface, so by using specific proteins I can look for particular sugars. There’s a dye attached to the protein, so when it sticks to the cell we can detect that using either a microscope or my favourite machine, the flow cytometer. The flow cytometer is a device that allows you to pass thousands of cells, one by one, past a laser and detect if the protein-dye is attached. I collect thousands of cellsworth of information and try to interpret it.
I’m from Cork, and I’ve been living in Dublin for six years. I’ve a BSc. in Biomedical Science, a Masters in Biomedical Diagnostics, and I started my PhD in 2011. In my spare time I do plenty of crochet, knitting and machine sewing. I use Linux on my laptop and do little bits of programming here and there. I’m an active member of TOG, the Dublin Hackerspace, where I turn up to the craftnight and help out on various projects such as the fabric cadaver and the twitter knitter. Me, wrestling the intestines of a prototype cadaver made at ScienceHackDay 2013.
My Typical Day: Feeding or killing cells, labelling cells, firing lasers at cells, sitting at the laptop
Most days I spent a chunk of time in front of my laptop, analysing data, looking for papers or trying to write up some of my work.
I have to feed cells two to three times a week. I have a flask of lymphocytes floating in media, and when they’ve used up the nutrients in the media and dropped out too much waste product, I need to put some of them in fresh media (and discard the rest that I don’t need).
Two days prior to an experiment, I prepare my cells by causing them to die by apoptosis. I then stain my cells, and go down to the flow cytometer to measure them. Then I get to analyse more data!
I also study my cells using western blots. I take the cells and add lots of detergent to break them down. I put them at the top of a gel and use electricity to drag the individual proteins through the gel. The proteins separate by size and I can use more electricity to transfer them onto a membrane which I can then stain to identify some properties of the proteins.
Some days I get to go to meetings or seminars.
What I'd do with the money: I’d book a fancy theatre for an outreach event I’ve wanted to run for aaaaaages
There’s a series of great standup/variety nights for scientists that get run in the UK, such as Science Showoff and Bright Club. I’d love to run one in Dublin, but with a super fancy theatrical venue.
How would you describe yourself in 3 words?
Feminist Hacker Scientist
Who is your favourite singer or band?
I don’t have one, as I don’t really listen to music
What's your favourite food?
Probably popcorn, it’s easy to make and you can go with plain butter and salt or go fancy with smoked paprika caramel with parmesan (very delicious)
What did you want to be after you left school?
A Scientist (any sort, initially a physicists, then a biomedical scientist)
Were you ever in trouble at school?
Plenty! I used to get very annoyed when I would be given out to for wearing trousers instead of the uniform skirt (sometimes I would arrive too late on my scooter to change into the skirt)
What was your favourite subject at school?
Science! For my leaving cert, I got to do physics, biology, chemistry AND applied maths. I was quite lucky, as a lot of people I’ve met since haven’t had the option on doing chemistry or physics, not to mind say all three science subjects!
What or who inspired you to become a scientist?
I spent a lot of time reading the science books in the library after I got bored of Nancy Drew and the Three Investigators. There was lots of books on the weather and space and dinosaurs, which I liked a lot.
If you weren't a scientist, what would you be?
If you had 3 wishes for yourself what would they be? - be honest!
I’d like to have a motorcycle again. I’d love an amazing kitchen with a proper oven (the oven in the place we’re renting is awful :( )
Tell us a joke.
Only one? … Why are bacteria rubbish at maths? …….. Because they multiply by dividing
The tissue culture suite, everything in the hood is sterile and must be kept like that. If it wasn’t sterile, bacteria would get into the flasks with the mamalian cells and out grow them
The inside of the flow cytometer. The DANGER ELECTRICITY door covers where cells can be sorted in droplets by giving each drop a charge and deflecting them with high voltage plates.
This is a common way to look at the proteins in a cell. The cell is lysed (disolved), its proteins are then separated on a gel using electricity and then stained so we can see them.
When you culture cells in a flask, you have ot make sure there aren’t too many. This is what I see when I count them when I feed them. Blue circles are dead cells, white circles are live cells. You count the number in the grid and multiply by the dilution factor to find out how many you have per mL.