Mia Brown: Making a Difference in the Lab
As children, we all wanted to be
firefighters, doctors, presidents, or princesses. If you were anything like me,
you just wanted to make a difference in people’s lives for the better. For a
while, I thought about being a pediatrician, then a nurse, then an optometrist,
then an oncologist, and finally a pharmacist. Once I reached college, I was
determined that was the job for me. I proceeded to start my college career as a
chemistry major with emphasis in pharmacy. I stuck to my guns about my career
choice until I started my break away. Unfortunately, I did not have the
opportunity to study abroad due to issues at home, so I decided to do something
local.
Over the summer of 2016, I started my
internship at the Greenwood Genetic Center at the research department. My
supervisor, Dr. Luigi Boccuto, is the assistant director of research looking at
autism and Phelan McDermid Syndrome, or PMS. As part of my job, I was to run sequences
of patient DNA to check for mutations in the 22q13 gene, which is believed to
be affiliated with autism and PMS. The first part of the summer was very
simple. I went through training and started performing my responsibilities.
The later part is when things became more difficult. My grandmother of 73 years old fell down the stairs and broke her femur. My father was deployed to Iraq, and my mother travels for work. My mother, brother, and I worked together to take care of her and my 93 year old great grandmother. To make sure they had food to eat, I would stay all morning to prepare breakfast and lunch for them, then go to the Greenwood Genetic Center. My mom and brother would take care of preparing dinner for them while I was away. Once we had our system in place, it was easy for me to keep going with all my responsibilities at the Greenwood Genetic Center and at home. I learned a lot about time management because of these unforeseen issues. I learned how to set up multiple experiments and run them all quickly and efficiently. I became so efficient, in fact, that I was able to keep up with the other interns even though I was there less often than they were.
The later part is when things became more difficult. My grandmother of 73 years old fell down the stairs and broke her femur. My father was deployed to Iraq, and my mother travels for work. My mother, brother, and I worked together to take care of her and my 93 year old great grandmother. To make sure they had food to eat, I would stay all morning to prepare breakfast and lunch for them, then go to the Greenwood Genetic Center. My mom and brother would take care of preparing dinner for them while I was away. Once we had our system in place, it was easy for me to keep going with all my responsibilities at the Greenwood Genetic Center and at home. I learned a lot about time management because of these unforeseen issues. I learned how to set up multiple experiments and run them all quickly and efficiently. I became so efficient, in fact, that I was able to keep up with the other interns even though I was there less often than they were.
One day, my supervisor came to me and
gave me a list of patient DNA samples and genes to run. He said he wanted them
done in a few days for the physician to be able to treat the patient. As I ran
my sequences, I came across something I was not prepared to see. I noticed a
mutation in one of our patients that I couldn’t find in the archive. At first I
thought I had made a mistake with the sequencing process, so I proceeded to
repeat the process and ended with the same results. I started to become a
little discouraged and went to my supervisor about the problem. When he saw
that the same exact mutation came up twice, he said that this was a real
mutation and not a mistake. He proceeded to look into what the mutation was,
and found that it was an extremely rare mutation. There is a 1/1,000 chance
that patients with PMS will have this specific mutation.
As I continued to look into the other patient DNA samples, I found the same mutation in another patient. When I reported the findings, my supervisor was able to send off the information to the physician properly treat the patients. This is when I discovered what I really wanted to do with my life.
As I continued to look into the other patient DNA samples, I found the same mutation in another patient. When I reported the findings, my supervisor was able to send off the information to the physician properly treat the patients. This is when I discovered what I really wanted to do with my life.
Finding those rare mutations and giving
the physician the information he/she needed to treat the patient gave me a
sense of euphoria. I knew that research was what I wanted to do. That moment
changed my whole perspective of my future for the better. I no longer felt
lost. From that moment, I started looking more and more into the chemistry of
what I was doing instead of the biology. I became curious about the proteins
being produced by the point mutations in the DNA and asked my supervisor to
clarify it for me. He explained that it is still being researched, and it is
very difficult to research.
I started looking more and more into how it is being researched, and it appeared to still be in the development stages. Nothing I saw seemed very concrete, so I started brainstorming my own ideas for fun. I had a fairly straight forward idea and began researching whether it might work or not. When I found no evidence of it ever being done, I started looking into how I would actually do the experiment. After a few weeks of research, I came up with my own hypothesis of testing proteins for their function using cadmium selenide quantum dots as a biological tag.
I started looking more and more into how it is being researched, and it appeared to still be in the development stages. Nothing I saw seemed very concrete, so I started brainstorming my own ideas for fun. I had a fairly straight forward idea and began researching whether it might work or not. When I found no evidence of it ever being done, I started looking into how I would actually do the experiment. After a few weeks of research, I came up with my own hypothesis of testing proteins for their function using cadmium selenide quantum dots as a biological tag.
By the time summer was over, I went to
Dr. Dukes in the chemistry department about my idea. He was impressed with the
new concept, since his specialty is in nanotechnology, specifically CdSe
nanoparticles. I began to continue my research at Lander University with Dr.
Dukes testing my theories. Instead of using CdSe, we ended up using gold
quantum dots since they were easier to synthesize. I picked a protein that we
already knew the function of that did not require other organelles or cells to
work.
The enzyme chosen was alcohol dehydrogenase, or ADH, which is used to break down alcohol in the body. This meant that I could make an enzyme assay using this protein and NAD+ to be reduced to NADH by the protein. The NADH content could be measured in a nanodrop that was generously provided by Dr. Lee in the biology department. In one of my solutions, I had the control setup with just the assay, and the other solution contained the quantum dots. I measured each solution every 5 minutes for 3 hours to see which solution produced the most NADH and at what rate. I found the solution with the quantum dots changed how well the enzyme functioned, which was exactly what I thought would happen.
From having completed my break away, I learned a lot about myself. I learned that I have an analytically creative mind. I can think of new ways to perform tasks that may or may not be more efficient. I learned that I am better at time management than I thought I was. Finally, I learned that even in the lab, not working directly with patients, you can still make a difference.
The enzyme chosen was alcohol dehydrogenase, or ADH, which is used to break down alcohol in the body. This meant that I could make an enzyme assay using this protein and NAD+ to be reduced to NADH by the protein. The NADH content could be measured in a nanodrop that was generously provided by Dr. Lee in the biology department. In one of my solutions, I had the control setup with just the assay, and the other solution contained the quantum dots. I measured each solution every 5 minutes for 3 hours to see which solution produced the most NADH and at what rate. I found the solution with the quantum dots changed how well the enzyme functioned, which was exactly what I thought would happen.
From having completed my break away, I learned a lot about myself. I learned that I have an analytically creative mind. I can think of new ways to perform tasks that may or may not be more efficient. I learned that I am better at time management than I thought I was. Finally, I learned that even in the lab, not working directly with patients, you can still make a difference.
Graduated
from Lander University in the spring of 2017 with a degree in Chemistry. During
her time at Lander University, she was a part of the jazz ensemble playing
tenor saxophone for all four years. She also tutored at the academic success
center her senior year in Calculus, Physics, Chemistry, and Statistics. For her
break away, she did an internship at the Greenwood Genetic Center in the
research department and continued her research at Lander University. Following
graduating, Mia will start her new job as a Chemistry teacher at Greenwood
District 50 in the fall of 2017. She plans to continue her education to get her
Master’s or Doctoral degree in chemical education to continue teaching and
continue her research at a University level.