Cell biology: Moving faster in a crowd

"Crowding is common in living systems at different length scales, from busy hallways down to dense cellular cytoplasm," said Ayusman Sen, Verne M. Willaman Professor of Chemistry and Distinguished Professor of Chemistry and Chemical Engineering at Penn State and one of the leaders of the research team. "The insides of cells are very, very crowded with proteins, macromolecules and organelles. Molecules that are involved in chemical reactions required by the cell must be transported through this crowded, viscous environment to find their partner reagents. If the environment is uniformly crowded, movement slows, but we know that the inside of a cell is non-uniform; there are gradients of macromolecules and other species. So, we were interested in how these gradients would influence transport at the nanoscale."

The researchers compared the movement of various "tracer" colloids -- insoluble particles suspended in a liquid -- through different environments using microfluidics. A microfluidic device can be filled with different solutions in which the researchers establish gradients -- from high to low -- of "crowder" macro-molecules in the fluid. The tracers, which can be large or small, hard or soft and deformable, are fluorescently labeled allowing the researchers to track their movement with a confocal microscope.

"We were surprised to see that the tracers moved faster in gradients of crowders than they did through a fluid with no crowders at all," said Farzad Mohajerani, a graduate student in chemical engineering at Penn State and co-first author of the paper. "We think that the densely packed crowders actually put a pressure on the tracers to force them toward less dense areas. Large tracer molecules moved faster than small ones, and soft, deformable tracers moved faster than hard ones."

"The soft, deformable tracers are better representatives of actual species moving around in cells," said Matthew Collins, a graduate student in chemistry at Penn State and co-first author of the paper. "We think that they can move faster because, unlike hard particles, they can squeeze through tighter areas."

"Our experiments and model not only show that molecules can move faster through gradients of macromolecular crowding, we think that these rates of movement may increase further inside actual living cells where other active moving molecules could increase the crowding pressure," said Sen.