Sequence-specific polyampholyte phase separation in membraneless organelles (1605.09019v2)

Abstract: Liquid-liquid phase separation of charge/aromatic-enriched intrinsically disordered proteins (IDPs) is critical in the biological function of membraneless organelles. Much of the physics of this recent discovery remains to be elucidated. Here we present a theory in the random phase approximation to account for electrostatic effects in polyampholyte phase separations, yielding predictions consistent with recent experiments on the IDP Ddx4. The theory is applicable to any charge pattern and thus provides a general analytical framework for studying sequence dependence of IDP phase separation.

Sequence-specific Polyampholyte Phase Separation in Membraneless Organelles

The paper "Sequence-specific polyampholyte phase separation in membraneless organelles" by Yi-Hsuan Lin, Julie D. Forman-Kay, and Hue Sun Chan, presents a significant advancement in understanding the biophysical properties contributing to phase separation of intrinsically disordered proteins (IDPs) within biological systems. The paper primarily focuses on elucidating the role of sequence-specific charge patterns in the phase behavior of IDPs, particularly polyampholytes, which consist of both positively and negatively charged monomers.

Summary of Research and Theoretical Framework

The authors build upon prior knowledge suggesting that many IDPs, despite lacking a fixed three-dimensional structure, are essential in various cellular functions due to their ability to form biomolecular condensates through phase separation. These include membraneless organelles that are crucial in cellular processes like signaling and gene regulation.

In this research, the authors propose a theoretical framework based on the random phase approximation (RPA) to address electrostatic interactions inherent in polyampholyte phase separation. The model accommodates any sequence-dependent charge pattern, providing a comprehensive analytical tool not only for experimental interpretations but also for exploring new IDP behaviors.

Notably, the paper applies this theoretical model to the IDP Ddx4, a well-researched protein known for its phase separation abilities in forming liquid-like droplets capable of influencing RNA dynamics. Experimental observations suggested that the phase separation of Ddx4 is highly dependent on its unique charge distribution, rather than merely its overall charge balance.

Key Numerical Results

The research quantifies the phase separation propensity between the wildtype Ddx4 and its charge-scrambled mutant, Ddx4$^{\rm N1}$CS. The paper calculates critical temperatures indicating a notable alteration upon charge scrambling. In quantitative terms, the wildtype Ddx4 displays a higher critical temperature and a diminished critical concentration compared to the mutant. This difference underscores the importance of specific charge sequences rather than net charge in dictating phase behavior.

Implications and Future Directions

The implications of this work are profound in both theoretical and practical aspects. The paper enhances the understanding of charge sequence-specific effects in IDP phase behavior, which is vital for the design of biomimetic materials and understanding pathological conditions where phase separation is disrupted.

Moreover, the theory, augmented by Flory-Huggins (FH) mean-field accounts for short-range interactions such as $\pi$-$\pi$ stacking, better reflects experimentally observed behaviors. This combination suggests that sequence information and non-electrostatic interactions are equally critical in understanding IDP phase separation, as highlighted by the results obtained for Ddx4$^{\rm N1}$.

Looking towards the future, the paper suggests exploration of other IDPs using the developed theoretical model to generalize its applicability. A natural progression would involve integrating additional specific interaction types into the model, to closely mimic biological environments.

This paper represents an essential step toward a deeper, sequence-level understanding of biomolecular condensation, with broader implications for cellular biology and materials science. The approach and resulting insights provide a framework for future investigations into how intrinsic sequence features dictate phase behaviors and the emergent properties of biologically relevant systems.