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      Confluence of Theory and Experiment Reveal the Catalytic Mechanism of the Varkud Satellite Ribozyme

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          Abstract

          The Varkud Satellite (VS) ribozyme catalyzes site-specific RNA cleavage and ligation, and serves as an important model system to understand RNA catalysis. Here we combine stereospecific phosphorothioate substitution, precision nucleobase mutation and linear free energy relationship measurements with molecular dynamics, molecular solvation theory, and ab initio quantum mechanical/molecular mechanical free energy simulations to gain insight into catalysis. Through this confluence of theory and experiment, we unify the existing body of structural and functional data to unveil the catalytic mechanism in unprecedented detail, including the degree of proton transfers in the transition state. Further, we provide evidence for a critical Mg 2+ ion in the active site that interacts with the scissile phosphate and anchors the general base guanine in position for nucleophile activation. This novel role for Mg 2+ adds to the diversity of known catalytic RNA strategies and unifies functional features observed in the VS, hairpin, and hammerhead ribozyme classes.

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          Most cited references52

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          Hachimoji DNA and RNA: A genetic system with eight building blocks

          We report DNA- and RNA-like systems built from eight nucleotide “letters” (hence the name “hachimoji”) that form four orthogonal pairs. These synthetic systems meet the structural requirements needed to support Darwinian evolution, including a polyelectrolyte backbone, predictable thermodynamic stability, and stereoregular building blocks that fit a Schrödinger aperiodic crystal. Measured thermodynamic parameters predict the stability of hachimoji duplexes, allowing hachimoji DNA to increase the information density of natural terran DNA. Three crystal structures show that the synthetic building blocks do not perturb the aperiodic crystal seen in the DNA double helix. Hachimoji DNA was then transcribed to give hachimoji RNA in the form of a functioning fluorescent hachimoji aptamer. These results expand the scope of molecular structures that might support life, including life throughout the cosmos.
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            Chemistry and Biology of Self-Cleaving Ribozymes.

            Self-cleaving ribozymes were discovered 30 years ago, but their biological distribution and catalytic mechanisms are only beginning to be defined. Each ribozyme family is defined by a distinct structure, with unique active sites accelerating the same transesterification reaction across the families. Biochemical studies show that general acid-base catalysis is the most common mechanism of self-cleavage, but metal ions and metabolites can be used as cofactors. Ribozymes have been discovered in highly diverse genomic contexts throughout nature, from viroids to vertebrates. Their biological roles include self-scission during rolling-circle replication of RNA genomes, co-transcriptional processing of retrotransposons, and metabolite-dependent gene expression regulation in bacteria. Other examples, including highly conserved mammalian ribozymes, suggest that many new biological roles are yet to be discovered.
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              • Article: not found

              Three-dimensional molecular theory of solvation coupled with molecular dynamics in Amber.

              We present the three-dimensional molecular theory of solvation (also known as 3D-RISM) coupled with molecular dynamics (MD) simulation by contracting solvent degrees of freedom, accelerated by extrapolating solvent-induced forces and applying them in large multi-time steps (up to 20 fs) to enable simulation of large biomolecules. The method has been implemented in the Amber molecular modeling package, and is illustrated here on alanine dipeptide and protein G.
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                Author and article information

                Journal
                101499734
                35773
                Nat Chem
                Nat Chem
                Nature chemistry
                1755-4330
                1755-4349
                16 November 2019
                20 January 2020
                February 2020
                29 July 2020
                : 12
                : 2
                : 193-201
                Affiliations
                [* ] Laboratory for Biomolecular Simulation Research, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8087, USA
                [] Institute for Quantitative Biomedicine, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8087, USA
                [] Department of Chemistry and Chemical Biology, Rutgers, The State University of New Jersey, Piscataway, NJ 08854-8087, USA
                [] Department of Chemistry, The University of Chicago, Chicago, IL 60637, USA
                [¥ ] Department of Biochemistry and Molecular Biology, The University of Chicago, Chicago, IL 60637, USA
                [§ ] Foundation for Applied Molecular Evolution, Firebird Biomolecular Sciences LLC, 13709 Progress Boulevard, Alachua, FL 32615, USA
                Author notes

                Author Contributions

                A.G. and B.P.W. contributed equally to this work. A.G. performed the computations and B.P.W. performed the experiments. A.G., B.P.W., J.A.P., and D.M.Y. co-wrote the paper. T.J.G. developed enabling software and provided technical support to various aspects of computational studies. N.L. synthesized phosphoramidites and oligonucleotides. S.H. and S.A.B. provided the hachimoji RNA substrate. S.R. characterized the stereochemistry of the phosphorothioate substrates. J.A.P. and D.M.Y. conceived and co-directed all experimental and computational aspects of the work. All correspondence and requests for materials should be addressed to J.A.P. and D.M.Y.

                Article
                NIHMS1543039
                10.1038/s41557-019-0391-x
                7389185
                31959957
                b3223e17-2662-4e43-8a4c-4d5c86356d4d

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                Chemistry
                Chemistry

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