Undergrad research – more fun for the professor?

Ever since I was a young undergraduate researcher at a small liberal arts college (SLAC), I knew that I wanted to work at a similar institution. Along the way, I have collaborated with some of the top scientists in my field, at large research-focused universities where a single researcher can get lost in a slew of graduate students and post-docs. Now that I’ve finished my first year teaching at McDaniel and I’m mentoring several undergraduate researchers, I know that I made the right choice.

Some of you might wonder “What’s so great about undergrad research?” Many PI’s (principal investigators; heads of research labs) prefer to have an army of researchers that are already trained to do the work on that lab’s specific project. Here are just some of the advantages of working with undergrads at McDaniel College.

Undergrad Enthusiasm

I am so impressed with the vigor with which my students dive into their projects. My style of mentoring is in line with the old adage “Give someone a fish, they eat for a day; teach someone to fish, they will eat for a lifetime.” I try to give my students the tools that they need to ask and answer their own questions. First I introduce them to a set of questions in line with my research program for which I think the student can yield some answers. I provide each student with some peer-reviewed literature to help them understand where their question “fits” into the broader picture and show them the techniques available to them in the Staab Lab.

Staab Lab June18, 2014

Katelyn McCabe processing larval fish specimens; Paola Villegas examining slides that she stained yesterday; Rachel Statler optimizing high speed videos; Sophia Fricke and Nick Azat preparing solutions for a histological stain.

Once they have these resources, the sky is the limit! The research this summer has truly been student driven, while I am in the background providing support (materials, advice on methods, training in scientific communication, etc.). Indeed, many of the techniques that are occurring in the lab this summer were brought to me by curious students, rather than my forcing methods on them. More importantly, the students are thinking deeply about their projects, asking spin-off questions, and chasing after those answers. It is thrilling to mentor them through this process.

Resourcefulness and sense of community at a SLAC

When an experiment requires expensive equipment or materials, we question the purchase more carefully than someone at a Research 1 university. In fact, many techniques can be modified so that we can bypass expensive purchases This resourcefulness helps us gain a deeper understanding of the protocols and the functionality of the equipment.

For example, in the Staab lab, we process tissue for histological techniques. Tissue processors are machines that automatically transfer a piece of tissue from one solution to the next, without you having to think much about the process. These machines cost about $50,000. But we can manually transfer the tissue into each solution, and if we understand why we are using each solution, we can better monitor how the temperature, timing, and chemistry of the solution are affecting the tissue.

Not only that, but there is a sense of collegiality and sharing among the research labs.

Here is another more simple example of resourcefulness (and a request!): specimen jars can cost hundreds of dollars from scientific supply stores, but why not save those empty pickle/pasta sauce/olive jars for our pickled fishes? It’s true what they say about one person’s trash…

Sample in a jar

Honing my own scientific skills

Let’s be honest, some of that undergrad enthusiasm leads to big dreams of projects that could fill three Ph.D dissertations. It’s my job to reel in the students and help them realize how to completely answer one question before moving on to the next one. It is tempting for all of us to jump to the next shiny project (SQUIRREL!) but it is important to complete each part of the puzzle before building upon it.

The human element

My reasons for getting into science are likely much different than those at a large research university and as such, my responsibilities differ here at McDaniel. Rather than focusing on grant proposals and a high output of data, I am more concerned that my students obtain a rich learning experience that will prepare them for a lifetime of answering questions. Little might they know, they are providing me with a similarly rich learning experience.

Dicty and the DNA Drama

This summer, I don’t even miss my shorts and flip-flops.  I prefer the lab coat, actually.

Each phase of the fruiting body formation is shown.

Dicty Fruiting Body Development

I have willingly traded summer essentials for lab gear and the opportunity to work with Dr. Parrish in her Dicty lab.  We have spent the past three and a half weeks working on Dictyostelium discoideum.  This social amoeba is fascinating, as it is unicellular when properly fed, but cells will aggregate and differentiate to form a multicellular fruiting body which will release spores once conditions improve.  For my particular project, I am focused on a gene similar to the L534 gene in Mimivirus.  This L534 gene is responsible for coding a mRNA decapping enzyme.  My interest is in characterizing this similar gene in Dicty by observing the phenotype of Dicty without this gene.

Cell cultures are displayed on a device used for counting the cell concentration.

AX3** cell culture on left and L534 KO cell culture on right, on a haemocytometer for cell counting. (Click for a larger image.)

Previous research students have created the Dicty L534* knockout, and my task is to study the impact of the L534 gene’s absence to develop a better understanding of the gene’s function and importance in Dicty’s development and survival.  There are three stages of my research which will provide details that we are seeking about the L534 gene in Dicty:

  1. Confirming the Knockout
  2. Observing Growth Rate
  3. Observing Cell Differentiation

The Dicty cultures have finally become healthy enough for completing these phases of the L534 knockout characterization, however, we have reached a snag in our master plan.  To confirm the success of the knockout, we must extract genomic DNA from the Dicty and amplify it though PCR as well as visualize it through gel electrophoresis.  We have completed the extraction and PCR, and we have run the gel, but much to our dismay, the DNA seem to have been degraded.  Confirming the knockout is imperative to the continuation of the L534 characterization, as without the proper knockout of L534, we could not study the effects of the gene.  And so, we have reached a determinant point.  We will be repeating the genomic DNA extraction, PCR, and gel, and the outcome will either “make it or break it.” Stay tuned for the resolution to our obstacle…


*For convenience, we call the gene of interest in Dicty “L534,” though this is the name of the similar gene in Mimivirus rather than the actual name of the gene in Dicty. **The AX3 Dicty cells will serve as the wild type as a means of comparison.  The AX3 cell culture is a strain of Dicty that can be grown axenically, meaning that it is grown on a nutritional substitute (HL5 medium) rather than the bacteria on which it normally feeds.

EPE Research: Florida and the First Training Week

During the last week in May I had the privilege of attending the annual conference of the American College of Sports Medicine (ACSM) in Orlando, Florida with Dr. McKenzie and Dr. Laird from our research team, along with my roommate for the trip, biomechanist, and avid Disney fan,  Mr. Petrie.  Dr. McKenzie and I presented a poster about our research from last summer.  We hope everyone at the conference enjoyed their lesson about the most physiologically beneficial method for walking on an inclined treadmill.  Some of the key points I learned are listed below:

  • The ACSM annual meeting covers a broad range of topics and features a number of sessions on the basic sciences
  • The conference itself is CRAZY with numerous sessions taking place at the same time and people dipping in and out of sessions at will.
  • For better health, focus on being active, not on weight or waist circumference
  • If you’re having trouble getting motivated to workout, make the activity a means to an end, rather the end itself (this includes taking stairs over elevators, standing more often, using your body as a mode of transportation- more than just your right foot, etc.)

During my week in Florida, the rest of the group faithfully finished all of the pre-testing such that we were able to stay on schedule and begin the training portion of our study this past week.  For the training portion of the study, participants were matched and subsequently randomized into two different training groups operating under the following conditions:

  • Standard training group- 3 min. at 60-65% maximum heart rate (max. HR), 27 min at 75-80% max. HR, 2 min. 60-65% max. HR
  • High Intensity Interval Training (HIIT) group- 3 min. at 60-65% max HR followed by four bouts of alternating 4 min. at 90-95% max. HR and 3 min. at 60-65% max. HR

Both protocols are designed such that total work is the same.  In both protocols, individuals arrive to the lab four times a week (Monday, Tuesday, Thursday, and Friday) to perform their training task for the day.  The beauty of using heart rate to measure intensity is that it accounts for days when the participant is feeling “off” and it adjusts the intensity as fitness level increases.  Already, we have noticed drastic differences in the ways that participants respond to the training load.  Most of the participants in the standard training protocol appear to have adjusted fairly well; while only about half of the participants in the HIIT protocol appear to have adjusted, the other half are in visible distress throughout most of their training sessions.  During one training session, a participant, having difficulty coping with the training, emphatically told me “I hate you Matt!”

Here’s to hoping we make it through another week of training visibly distressed HIIT participants.

-Matt Peterson (HIIT team)

So ‘Sexta Can Wait

[Hey, this is Meg; It says Amanda because she logged in for me.]

My project is finally underway after several issues with the set-up. I had started out with the first group of manduca in their boxes, but they decided to make like Houdini and disappear on me. So I got a new group of eggs and set them up in tubes to grow until they are too large to escape. I had to wait what felt like a week for them to hatch, but finally they are all hatched and growing. Most have reached second instar by now, and pretty soon I will be moving them to their boxes.

None have reached third instar yet, when I will take their measurements and record their responses to being handled. So right now, I am just waiting for the little darlings to grow bigger so I can move on to the next part of the project. However, today I did notice that two partnered caterpillars were going at it in their tube: the larger one chasing the smaller one around and biting him. This seems to be unusual, as I have not observed it with any of the others; usually they bite when their face randomly ends up near another caterpillar’s body, but this particular bully seemed to have ill intention. We shall see if this has any effect on either of their responses later.

Fishing & Feeding in the Larval Behavior Lab

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Summer is one of my favorite times at McDaniel, because this is when I put aside the demands of teaching, and the administrative chores of being a professor, and get to focus on research with students!  This summer the Jacobs lab is focusing on larval behavior and feeding in two very different systems: dragonfly larvae, and tobacco hornworms.  I’ll let the student researchers introduce their specific questions in later blog posts, but for now I’ll introduce the teams:

IMG_20140529_111850540_HDRJosh Viar and Meghan Sturgill are my field team – they are spending the summer investigating the distribution and behavior of dragonfly larvae in a range of local ponds.  Their project is entirely field-based, and involves hunting in the mud for dragonfly larvae, observing their behavior for hours in large floating arenas, and sampling for fish with minnow traps and fishing poles.  In other words, if you like to splash around outdoors and aren’t afraid of a little mud, they have designed the perfect summer project!

IMG_20140604_130838675Meg Knauff and Amanda Horst are my lab team – they are spending the summer investigating the effects of diet on growth, feeding, and behavior of the tobacco hornworm, Manduca sexta.  They have designed an ambitious and labor-intensive project, and are working in close collaboration to make it happen.  This was a project they started in my larval biology course in the spring, and it was so interesting that we just had to continue it over the summer!

Greta_fishingFinally, every lab needs a mascot!  My daughter Greta (7 months) sometimes visits my office or comes along on field work.  As a working mom, I’m grateful for the more flexible schedule of summer, which allows me to spend more time with her, and to McDaniel for being a supportive workplace for women in science!  So far we haven’t put her to work fishing, but she’s ready!