Scientists have a better understanding of a mechanism that
allows cells to internalize beneficial nutrients and not-so-beneficial viruses,
thanks to collaboration among researchers from two South Dakota universities
and the National Institutes of Health.
South
Dakota State University associate professor Adam Hoppe, South Dakota School of
Mines & Technology professor Steve Smith and NIH scientists Justin Taraska
and Kem Sochacki combined three unique types of microscopy to track how a protein
called clathrin triggers cell membrane bending. They found that clathrin, which
creates a honeycomb shaped scaffold on the cell membrane, has an unexpected
amount of plasticity when pinching off small portions of the cell membrane.
Their work was published in the Jan. 29, 2018, issue of Nature Communications.
Hoppe
and Smith work collaboratively through the South Dakota BioSystems Networks and
Translational Research (BioSNTR)
center, which is funded through the South Dakota Research Innovation Center
program and the National Science Foundation’s Established Program to Stimulate Competitive Research program.
A greater understanding of how cells internalize material will help BioSNTR researchers
working with Sioux Falls-based SAB Biotheraputics to develop new alternative
treatments for influenza.
The
contributions of NIH scientists Justin Taraska and Kem Sochacki were made
possible through a federally funded intramural research program.
“It was an awesome team science effort and an
important model for success,” said Hoppe, a cell biologist and BioSNTR director. His
research focuses on developing antiviral and anticancer therapeutics.
“This is a
fundamental ‘how does the cell work’ kind of question that has radiating
impacts on a multitude of disease processes and important physiological
functions in plants, animals and humans,” Hoppe explained. “The process, known
as endocytosis, is one of the main mechanisms by which cells internalize
material from the environment and remodel their surfaces.”
Hoppe and his team essentially filmed live cells internalizing
their own membrane using fluorescence on a nanoscale. Then they used a laser
beam to differentiate horizontal and vertical orientations and chemically froze
the cells at various stages to capture high-resolution images of membrane
bending.
“Endocytosis in human cells is primarily driven by clathrin,
which forms a honeycomb lattice that grabs a piece of membrane and pulls it
inside the cell. Viruses hijack this process to get into cells; it’s also how many
drugs are delivered into a cell,” explained Taraska, a senior investigator in
the Laboratory of Molecular and Cellular Imaging at the National Heart, Lung
and Blood Institute, part of the NIH. He and his team scanned the cells using
super resolution light imaging with fluorescence and electron microscopy,
correlating the two by laying one image on top of the other.
Smith, a physicist and director of the SD Mines nanoscience
and nanoengineering program, said, “This a big technical accomplishment. Three
teams separated by thousands of miles examined the same cell, down to the
nanometer level— that’s an incredible accomplishment!”
He and his team used atomic force microscopy to precisely
measure the clathrin structure and resulting vesicles, including their height
and diameter. Each cell had 50 to 100 vesicles.
The three-pronged approach gave the researchers confidence in
their findings—and their collaboration is continuing.
“This collaboration was unique, combining three advanced
techniques and taking advantage of everyone’s unique expertise,” Taraska said.
“It worked because everyone was sharing and coming together to tackle a single important
problem.”
Smith agreed, “BioSNTR brings people together with different
kinds of tools and expertise to shed light on processes that we don’t
understand. It’s about forming a team and giving them a mission.”