CHAMPAIGN,
Ill. -- Scientists have developed an extremely accurate
imaging technique for looking inside the machinery of a
cell and have found that molecules of myosin "walk" in a
fashion very much like a human.
"Myosin
walks like we walk, but with a 74-nanometer stride that
is more than 10 million times smaller than ours," said Paul
Selvin, a professor of physics at the University of Illinois
at Urbana-Champaign and corresponding author of a paper
to appear in the journal Science, as part of the Science
Express Web site, on June 5.
Myosin
is a tiny molecular motor that converts chemical energy
into mechanical motion. While there are more than a dozen
types of myosin (including myosin II – the main protein
responsible for muscle contractions), Selvin and his collaborators
studied myosin V.
"This
protein is also responsible for movement," Selvin said,
"But not muscular movement. Myosin V is a little cargo transporter
in our cells that moves things around by stepping along
filaments of actin."
Myosin
V is particularly prevalent in nerves. For this reason,
mutations in the protein can lead to seizures and other
neurological problems. "Like many other biomolecular motors,
Myosin V is amazing," Selvin said. "It's tiny, but strong.
It can carry more than 1,000 times its own weight."
Myosin
V has two "legs" connected to a "body," but exactly how
the protein molecule moves its load along helical fibers
of actin has been a mystery. "Studies have suggested two
main models for movement," Selvin said. "One is the hand-over-hand
(or foot-over-foot) 'walking' model in which the two feet
alternate in the lead. The other model is the 'inchworm'
model in which one foot always leads."
The
two models predict significantly different step sizes, Selvin
said, but previous imaging techniques have lacked the resolution
necessary to measure the step size and determine which model
is correct. To measure such minuscule motion, Selvin and
his Illinois colleagues -- physics professor Taekjip Ha
and graduate students Ahmet Yildiz and Sean McKinney --
developed a single-molecule imaging technique that is capable
of locating the position of a fluorescent dye to within
1.5 nanometers. (One nanometer is a billionth of a meter,
or about 10,000 times smaller than the width of a human
hair). This localization represents a 20-fold improvement
over other techniques that use fluorescent dyes.
The
researchers also found a way to extend the lifetime of the
dye from a few seconds to several minutes. Then they teamed
up with physiology professor Yale Goldman and postdoctoral
researcher Joseph Forkey, both at the University of Pennsylvania,
in applying the technique to measuring myosin movement.
"First,
we attach a little fluorescent dye to one of the feet and
we take a picture with a digital camera attached to a microscope
to find exactly where the dye is," Selvin said. "Then we
feed the myosin a little food called adenosine triphosphate,
and it takes a step. We take another picture, locate the
dye, and accurately measure how far the dye moved."
By looking
at the step size, the scientists can tell whether the protein
is walking or inchworming along, Selvin said. If it is walking,
the rear foot takes twice as big a step than if it were
inchworming.
"The
long dye lifetime allowed us to measure many consecutive
steps, which occurred about once every 3 seconds," Selvin
said. "The foot wearing the dye would move forward 74 nanometers,
then pause while the unlabeled foot moved forward. The cycle
would then repeat itself. The 74-nanometer step size we
measured is consistent with a hand-over-hand walking mechanism
and inconsistent with an inchworm mechanism."
As an
additional check, the researchers also labeled the myosin
higher up on the leg, "somewhere in the neighborhood of
the thighbone," Selvin said. "The steps alternated in size
between long and short, just as you'd expect if it was walking.
An inchworm motion, on the other hand, would always yield
the same step size, and so we could rule that out."
There
are hundreds of different types of biomolecular motors,
involved in everything from muscle contraction to moving
chromosomes during cell division, to reloading necessary
ammunition within nerve cells so they can repeatedly fire.
"The cell is a busy place, much like a city where things
are constantly moving around," Selvin said. "It will be
interesting to see whether all the motors move in the same
way."