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Rosana Collepardo-Guevara

Researcher at University of Cambridge

Publications -  69
Citations -  2381

Rosana Collepardo-Guevara is an academic researcher from University of Cambridge. The author has contributed to research in topics: Chemistry & Biology. The author has an hindex of 19, co-authored 48 publications receiving 1459 citations. Previous affiliations of Rosana Collepardo-Guevara include National Autonomous University of Mexico & New York University.

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Bimolecular reaction rates from ring polymer molecular dynamics: Application to H + CH4→ H2 + CH3

TL;DR: The results indicate that the previous assessment of the accuracy of the RPMD approximation for atom-diatom reactions remains valid for more complex polyatomic reactions, and suggest that the sensitivity of the QTST and QI rate coefficients to the choice of the transition state dividing surface becomes more of an issue as the dimensionality of the reaction increases.
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Liquid network connectivity regulates the stability and composition of biomolecular condensates with many components

TL;DR: The physical parameters dictating the stability and composition of multicomponent biomolecular condensates are investigated using a minimal coarse-grained model and it is demonstrated that the molecular connectivity of the condensed-liquid network determines the stability (e.g., in temperature, pH, salt concentration), where stability is positively correlated with connectivity.
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Bimolecular reaction rates from ring polymer molecular dynamics.

TL;DR: An efficient procedure for calculating the rates of bimolecular chemical reactions in the gas phase within the ring polymer molecular dynamics approximation, which is illustrated with applications to the three-dimensional H + H(2), Cl + HCl, and F + H
Posted ContentDOI

Reentrant liquid condensate phase of proteins is stabilized by hydrophobic and non-ionic interactions

TL;DR: It is shown that proteins implicated in cellular LLPS, including FUS, TDP-43, Brd4, Sox2, and Annexin A11, which form condensates at low salt concentrations, can reenter a phase-separated regime at high salt concentrations.