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  1. Article ; Online: In Vitro Evolution Reveals Noncationic Protein-RNA Interaction Mediated by Metal Ions.

    Giacobelli, Valerio G / Fujishima, Kosuke / Lepšík, Martin / Tretyachenko, Vyacheslav / Kadavá, Tereza / Makarov, Mikhail / Bednárová, Lucie / Novák, Petr / Hlouchová, Klára

    Molecular biology and evolution

    2022  Volume 39, Issue 3

    Abstract: RNA-peptide/protein interactions have been of utmost importance to life since its earliest forms, reaching even before the last universal common ancestor (LUCA). However, the ancient molecular mechanisms behind this key biological interaction remain ... ...

    Abstract RNA-peptide/protein interactions have been of utmost importance to life since its earliest forms, reaching even before the last universal common ancestor (LUCA). However, the ancient molecular mechanisms behind this key biological interaction remain enigmatic because extant RNA-protein interactions rely heavily on positively charged and aromatic amino acids that were absent (or heavily under-represented) in the early pre-LUCA evolutionary period. Here, an RNA-binding variant of the ribosomal uL11 C-terminal domain was selected from an approximately 1010 library of partially randomized sequences, all composed of ten prebiotically plausible canonical amino acids. The selected variant binds to the cognate RNA with a similar overall affinity although it is less structured in the unbound form than the wild-type protein domain. The variant complex association and dissociation are both slower than for the wild-type, implying different mechanistic processes involved. The profile of the wild-type and mutant complex stabilities along with molecular dynamics simulations uncovers qualitative differences in the interaction modes. In the absence of positively charged and aromatic residues, the mutant uL11 domain uses ion bridging (K+/Mg2+) interactions between the RNA sugar-phosphate backbone and glutamic acid residues as an alternative source of stabilization. This study presents experimental support to provide a new perspective on how early protein-RNA interactions evolved, where the lack of aromatic/basic residues may have been compensated by acidic residues plus metal ions.
    MeSH term(s) Amino Acids/genetics ; Ions ; Molecular Dynamics Simulation ; RNA/genetics
    Chemical Substances Amino Acids ; Ions ; RNA (63231-63-0)
    Language English
    Publishing date 2022-02-01
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 998579-7
    ISSN 1537-1719 ; 0737-4038
    ISSN (online) 1537-1719
    ISSN 0737-4038
    DOI 10.1093/molbev/msac032
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Laccase-based synthesis of SIC-RED

    Giacobelli, Valerio G. / Pezzella, Cinzia / Sannia, Giovanni / Olivieri, Giuseppe / Fontanarosa, Carolina / Amoresano, Angela / Piscitelli, Alessandra

    Biocatalysis and Agricultural Biotechnology

    A new dyeing product for protein gel staining

    2018  Volume 15

    Abstract: In the last years, laccases have become leading biocatalysts in green bioprocesses for dye synthesis. Among fungal laccases, the high-redox potential laccase POXA1b from Pleurotus ostreatus is a valuable candidate since it brings together several key- ... ...

    Abstract In the last years, laccases have become leading biocatalysts in green bioprocesses for dye synthesis. Among fungal laccases, the high-redox potential laccase POXA1b from Pleurotus ostreatus is a valuable candidate since it brings together several key-elements: stability and activity in a wide range of pHs and temperatures and the availability of a cost-effective bioprocess for its production. In this work POXA1b catalyzed the coupling of a p-phenylenediamine and α-naphtol, resulting in the production of a new dyeing product, named SIC-RED. The dye was structurally characterized and its performances in protein gel staining tested. The economic feasibility of the process was demonstrated in the case of an Italian small medium enterprise. The results let envisage a real exploitation of the herein enzymatically synthesized dye for protein gel staining.
    Keywords Dye synthesis ; Economic analysis ; High-redox potential laccase ; Protein gel staining ; Proteomics
    Subject code 540
    Language English
    Publishing country nl
    Document type Article ; Online
    ZDB-ID 2642052-1
    ISSN 1878-8181
    ISSN 1878-8181
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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