This summer I had the opportunity
to visit the Albert Einstein College of Medicine in New York City, in order to
gain new research experiences outside my normal field of study. My normal
research in Dr. Zangle’s lab at UCLA involves studying the mechanical
properties of cells, but this summer I will be learning biochemical techniques
in the context of protein engineering and characterization.
This was my first week of research
at the Albert Einstein College of Medicine and already the experience is so
different from anything I could have expected. one of the really surprising
things to me is that pipette tips are not considered sharps (even the
serological pipettes, which was shocking to me). It has been a good experience
so far; this is my first time working in a biochemistry lab. We use a technique
in the lab called phage display to create novel proteins through directed
evolution. By inducing mutations in e.
coli, and repackaging the DNA into phage particles, we are able to then
select for the phage expressing our protein of interest. By repeating this
process over and over, we can continue to select for phage with increased
binding affinity to our protein of interest. The first week went well, but I am
still getting the hang of the laboratory techniques used in the lab, bacterial
cell culture, and phage selection.
The first weekend I decided that
since I am in New York for the summer I should try to make the most of this
opportunity. As such I decided to take the train down to Princeton University
in New Jersey, and went for a walk around the campus. It was really fun and
while I was there I had an opportunity to have dinner with my cousin Sarah who
I had not seen in years. Overall it was a good weekend and a good first week in
New York.
Picture Captions:
Picture 1: Albert Einstein College of Medicine, located in
the Bronx.
Picture 2: Automatic sonicator for lysing cells and
fragmenting DNA. We use this instead of detergent so that DNA does not gunk up
our mixture, and because the protein we are interested in isolating from the e.
coli needs to be released from occlusion bodies in the cell.
Picture 3: So my normal cell culture experience involves
using a biosafety hood and extremely sanitary conditions. This is my first time
doing cell culture on a bench top using a flame to maintain sanitary
conditions.
Picture 4: This is the first time I have ever had to run a
gel (in this case a western blot). It is so much harder to do than LS3 prepared
me for. Interpreting the data is relatively straightforward but not breaking
the gel is an art form.
Picture 5: View crossing over the Harlem River from the
Bronx into Manhattan.
Picture 6: Whitman College of Princeton University.
Princeton was really beautiful and I really enjoyed spending the day there. The
mixed architecture (has elements from the Gothic and Romanesque periods as well
as a few others) is awesome as well, and so much different the Romanesque
architecture at UCLA.
Picture 7: This is a walkway at Princeton just behind
Whitman College. The university is so beautiful, it is hard not to just post
all my pictures that I took (although I posted them on facebook so if you are
interested you can see them all there).
So far this has been an awesome experience and I can’t wait
to start again this week!
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