Effect of Protein Environment on the Shape Resonances of RNA Nucleobases: Insights From a Model System

Fuente: arXiv
Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Arora, Sneha, J, Jishnu Narayanan S, Haritan, Idan, Adhikary, Amitava, Dutta, Achintya Kumar
Format: Preprint
Veröffentlicht: 2025
Schlagworte:
Online-Zugang:
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
_version_ 1866911026988974080
author Arora, Sneha
J, Jishnu Narayanan S
Haritan, Idan
Adhikary, Amitava
Dutta, Achintya Kumar
author_facet Arora, Sneha
J, Jishnu Narayanan S
Haritan, Idan
Adhikary, Amitava
Dutta, Achintya Kumar
contents In this work, the effect of amino acid environment on the nucleobase-centered anion radical shape resonances is investigated by employing uracil as a model system for pyrimidine base in RNA. Anionic uracil-glycine complexes have been used to model the RNA-protein interactions. The resonance positions and widths of these complexes have been simulated using the equation of motion coupled cluster method coupled with resonance via Padé approach. Our work shows that in the transient negative ion (TNI, or, the anion radical of glycine:uracil complex), glycine stabilizes the nucleobase-centered resonances through hydrogen bonding, increasing the lifetime of TNI. At the same time, a glycine-centered resonance shows the ability of amino acids to capture the electron density and move it away from the uracil nucleobase. At the micro-solvation level, this modeling indicates that amino acids would have more influence on nucleobase-centered resonances in the TNI than that displayed by the corresponding aqueous environment.
format Preprint
id arxiv_https___arxiv_org_abs_2505_01020
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Effect of Protein Environment on the Shape Resonances of RNA Nucleobases: Insights From a Model System
Arora, Sneha
J, Jishnu Narayanan S
Haritan, Idan
Adhikary, Amitava
Dutta, Achintya Kumar
Chemical Physics
In this work, the effect of amino acid environment on the nucleobase-centered anion radical shape resonances is investigated by employing uracil as a model system for pyrimidine base in RNA. Anionic uracil-glycine complexes have been used to model the RNA-protein interactions. The resonance positions and widths of these complexes have been simulated using the equation of motion coupled cluster method coupled with resonance via Padé approach. Our work shows that in the transient negative ion (TNI, or, the anion radical of glycine:uracil complex), glycine stabilizes the nucleobase-centered resonances through hydrogen bonding, increasing the lifetime of TNI. At the same time, a glycine-centered resonance shows the ability of amino acids to capture the electron density and move it away from the uracil nucleobase. At the micro-solvation level, this modeling indicates that amino acids would have more influence on nucleobase-centered resonances in the TNI than that displayed by the corresponding aqueous environment.
title Effect of Protein Environment on the Shape Resonances of RNA Nucleobases: Insights From a Model System
topic Chemical Physics
url https://arxiv.org/abs/2505.01020