TY - JOUR
T1 - Relation between single-molecule properties and phase behavior of intrinsically disordered proteins
AU - Dignon, Gregory L.
AU - Zheng, Wenwei
AU - Best, Robert B.
AU - Kim, Young C.
AU - Mittal, Jeetain
N1 - Publisher Copyright:
© 2018 National Academy of Sciences. All rights reserved.
PY - 2018/10/2
Y1 - 2018/10/2
N2 - Proteins that undergo liquid-liquid phase separation (LLPS) have been shown to play a critical role in many physiological functions through formation of condensed liquid-like assemblies that function as membraneless organelles within biological systems. To understand how different proteins may contribute differently to these assemblies and their functions, it is important to understand the molecular driving forces of phase separation and characterize their phase boundaries and material properties. Experimental studies have shown that intrinsically disordered regions of these proteins are a major driving force, as many of them undergo LLPS in isolation. Previous work on polymer solution phase behavior suggests a potential correspondence between intramolecular and intermolecular interactions that can be leveraged to discover relationships between single-molecule properties and phase boundaries. Here, we take advantage of a recently developed coarse-grained framework to calculate the θ temperature Tθ, the Boyle temperature TB, and the critical temperature Tc for 20 diverse protein sequences, and we show that these three properties are highly correlated. We also highlight that these correlations are not specific to our model or simulation methodology by comparing between different pairwise potentials and with data from other work. We, therefore, suggest that smaller simulations or experiments to determine Tθ or TB can provide useful insights into the corresponding phase behavior.
AB - Proteins that undergo liquid-liquid phase separation (LLPS) have been shown to play a critical role in many physiological functions through formation of condensed liquid-like assemblies that function as membraneless organelles within biological systems. To understand how different proteins may contribute differently to these assemblies and their functions, it is important to understand the molecular driving forces of phase separation and characterize their phase boundaries and material properties. Experimental studies have shown that intrinsically disordered regions of these proteins are a major driving force, as many of them undergo LLPS in isolation. Previous work on polymer solution phase behavior suggests a potential correspondence between intramolecular and intermolecular interactions that can be leveraged to discover relationships between single-molecule properties and phase boundaries. Here, we take advantage of a recently developed coarse-grained framework to calculate the θ temperature Tθ, the Boyle temperature TB, and the critical temperature Tc for 20 diverse protein sequences, and we show that these three properties are highly correlated. We also highlight that these correlations are not specific to our model or simulation methodology by comparing between different pairwise potentials and with data from other work. We, therefore, suggest that smaller simulations or experiments to determine Tθ or TB can provide useful insights into the corresponding phase behavior.
KW - Intrinsically disordered proteins
KW - Liquid-liquid phase separation
KW - Membraneless organelles
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U2 - 10.1073/pnas.1804177115
DO - 10.1073/pnas.1804177115
M3 - Article
C2 - 30217894
AN - SCOPUS:85054376040
SN - 0027-8424
VL - 115
SP - 9929
EP - 9934
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 40
ER -