The spontaneous self-assembly of proteins and nucleic acids into biomolecular condensates has been shown to ubiquitously contribute to the functional compartmentalization of the cell. However, their liquid-to-solid transformation (i.e., aging) driven by interprotein β-sheet transitions represents a hallmark of multiple neurode-generative disorders. We perform molecular dynamics simulations to elucidate the role of different biomolecules in regulating the aging kinetics of TDP-43, an RNA-binding protein linked to amyotrophic lateral sclerosis and frontotemporal dementia. We find that while arginine-rich peptides accelerate the nucleation of interprotein β-sheet structures, the inclusion of RNAs and the HSP70 chaperone slows down their emergence. Interestingly, we observe a correlation between the protein compactness—governed by the condensate composition—and aging kinetics. Moreover, we find that near-interfacial regions of TDP-43 condensates exhibit faster interprotein transitions than the core of the condensate. Together, our findings underscore the major role of client biomolecules in controlling the propensity of multicomponent condensates to form harmful solidlike states.
The spontaneous self-assembly of proteins and nucleic acids into biomolecular condensates has been shown to ubiquitously contribute to the functional compartmentalization of the cell. However, their liquid-to-solid transformation (i.e., aging) driven by interprotein β-sheet transitions represents a hallmark of multiple neurode-generative disorders. We perform molecular dynamics simulations to elucidate the role of different biomolecules in regulating the aging kinetics of TDP-43, an RNA-binding protein linked to amyotrophic lateral sclerosis and frontotemporal dementia. We find that while arginine-rich peptides accelerate the nucleation of interprotein β-sheet structures, the inclusion of RNAs and the HSP70 chaperone slows down their emergence. Interestingly, we observe a correlation between the protein compactness—governed by the condensate composition—and aging kinetics. Moreover, we find that near-interfacial regions of TDP-43 condensates exhibit faster interprotein transitions than the core of the condensate. Together, our findings underscore the major role of client biomolecules in controlling the propensity of multicomponent condensates to form harmful solidlike states. Read More
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