New study sheds light on molecular machinery of nervous system
A University of Arkansas research team shed new light on the molecular properties that drive the nervous system. Their work was recently published in Biochemistry, one of the top journals in the field. Kelsey Sparks, an alumna of the J. William Fulbright College of Arts and Sciences and the Honors College, who is currently pursuing a medical degree at the University of Arkansas for Medical Sciences, led the research effort as an undergraduate, working for three years on what became her capstone honors thesis.
Sparks is the first author on the article, giving her primary credit for the discoveries. Other undergraduate coauthors were Fulbright and Honors College alumna and Sturgis Fellow Rebekah Langston, who currently holds a research position at the National Institutes of Health, and Renatra Gist, an alumna of Tennessee State University who completed a summer National Science Foundation-sponsored Research Experience for Undergraduates at the U of A.
The paper, "Comparisons of Interfacial Phe, Tyr, and Trp Residues as Determinants of Orientation and Dynamics for GWALP Transmembrane Peptides," was featured on the front of Biochemistry's website, an unprecedented honor for undergraduate work, according to honors faculty mentor Roger Koeppe, Distinguished Professor of chemistry.
"It was a nice surprise when Dr. Koeppe emailed me," Sparks said. "It's an honor to have our research published in Biochemistry."
Using nuclear magnetic resonance spectroscopy, the U of A team altered the amino acid sequences of model peptides and incorporated deuterium labels to study how they move within a model for the outer membrane of a cell.
"It's like doing an MRI on a molecule," Koeppe said.
Several of their findings were surprising: for example, some of the amino acids that could form hydrogen bonds with membrane lipids caused their host helices to move faster than their non-hydrogen bonding counterparts.
"You would think that hydrogen bonds would slow things down, since water is slower than gas," Koeppe said. The team also discovered that peptide rotations are sensitive to changes in the thickness of membranes. The paper contributes to knowledge of the molecular properties that allow the nervous system to work, and ultimately could contribute to the understanding and treatment of neurological diseases such as Alzheimer's or Parkinson's.
"We're working at the first level – the physics of it," Koeppe cautioned. "We're not developing medical products, but we're trying to improve the basic understanding. The remarkable thing is that these undergraduate students were making discoveries in such a complex area. They're at the forefront in this field."
The Honors College supported Sparks' work with a research and travel grant. Other members of the research team who are coauthors on the article are Nicholas J. Gleason, Denise V. Greathouse and Koeppe.
Research on the molecular frontier of membrane biophysics continues in Koeppe's lab, where five Honors College students are currently exploring additional questions related to the research published in Biochemistry.
More information: "Comparisons of Interfacial Phe, Tyr, and Trp Residues as Determinants of Orientation and Dynamics for GWALP Transmembrane Peptides." Kelsey A. Sparks, Nicholas J. Gleason, Renetra Gist, Rebekah Langston, Denise V. Greathouse, and Roger E. Koeppe, II. Biochemistry 2014 53 (22), 3637-3645 DOI: 10.1021/bi500439x
Journal information: Biochemistry
Provided by University of Arkansas