Co-corresponding authors Tanja Mittag, Ph.D., and Erik Martin, Ph.D., both of the Department of Structural Biology, are studying how liquid-liquid phase separation may ultimately lead to opportunities to therapeutically target parts of the process that may be involved in neurodegenerative diseases.
Scientists at St. Jude Children’s Research Hospital are studying liquid-liquid phase separation (LLPS), a biophysical process through which proteins and nucleic acids in a cell are compartmentalized without a membrane. The work provides new insight into how the strength of the forces that drive phase separation are linked to the speed at which it occurs. The findings were published today in Nature Communications.
Cells need to sort and organize proteins and other components. One way they do so is through LLPS, a process similar to the way oil forms droplets in water. Membraneless organelles, bodies in a cell that behave like liquid droplets, organize certain proteins without enclosing them with a membrane. Instead, the proteins are held together by the biophysical forces that drive LLPS.
Little is known about how biomolecules transition from a one-phase solution to a two-phase mixture, in a process called nucleation. This process has been challenging to evaluate because it requires looking at extremely fast time scales (microseconds to milliseconds). As a result, most studies have looked instead at evolution within systems that are already in the two-phase regime (how droplets fuse and grow).
“We can see during these very early time points that even individual disordered protein molecules that phase separate have quite different properties than disordered proteins that don't phase separate,” said co-corresponding author Tanja Mittag, Ph.D., St. Jude Department of Structural Biology.
Research at St. Jude and elsewhere has shown that LLPS can be involved in neurodegenerative diseases such as amyotrophic lateral sclerosis (ALS) and cancer. A better understanding of LLPS may ultimately lead to opportunities to therapeutically target parts of the process.
Microsecond time measurements give new understanding
The prevailing view of LLPS in biology has been that a change in cellular conditions can spontaneously lead to nucleation, switching a single-phase solution into two phases. In this research, the scientists used a simplified system, with a single protein in water and salt, to study whether the switch actually occurred in such a manner or if additional steps are required to kickstart the process.
With a technique called rapid mixing, time-resolved, small-angle X-ray scattering (TR-SAXS), the researchers were able to observe the earliest stages of the process. They examined the nucleation of a prion-like domain called A1-LCD from the protein hnRNPA1. Mutations of this protein cause ALS and other diseases.
The scientists showed how clusters of A1-LCD form, and how these clusters lead to LLPS. The findings indicate that nucleation contains distinct steps, differentiated by the size of the cluster. When looking at the smallest clusters (with few individual molecules), scientists found that the assembly behavior differed from classical nucleation theory. These deviations potentially explain why phase separation of some biomolecules can happen in milliseconds while it takes hours for others.
“Even in a simplified system, you still have to take into account these kind of non-ideal effects at the early stages of nucleation,” said co-corresponding author Erik Martin, Ph.D., St. Jude Department of Structural Biology. “Before you can start thinking about phase separation assembly or condensation in cells, you need to think about things from a molecular level. There are going to be initial steps to that assembly that aren’t accounted for in previous models.”
Authors and funding
The other authors are Tyler Harmon, the Max Planck Institute for the Physics of Complex Systems; Jesse Hopkins and Srinivas Chakravarthy, Illinois Institute of Technology; J. Jeremias Incicco and Andrea Soranno, Washington University in St. Louis; and Peter Schuck, National Institute of Biomedical Imaging and Bioengineering.
The study used resources facilitated by the National Institute of General Medical Sciences and was funded by a grant from the National Institutes of Health (R01NS121114), the Intramural Research Programs of the National Institute of Biomedical Imaging and Bioengineering, the St. Jude Research Collaborative on the Biology of Liquid Organelles and ALSAC, the fundraising and awareness organization of St. Jude.
St. Jude Children's Research Hospital
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