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Magnesium ion-driven folding and conformational switching kinetics of tetracycline binding aptamer: implications for in vivo riboswitch engineering

Kaiser, Christoph ; Vogel, Marc ; Appel, Bettina ; Weigand, Julia ; Müller, Sabine ; Suess, Beatrix ; Wachtveitl, Josef (2023)
Magnesium ion-driven folding and conformational switching kinetics of tetracycline binding aptamer: implications for in vivo riboswitch engineering.
In: Journal of molecular biology, 435 (20)
doi: 10.1016/j.jmb.2023.168253
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

Engineering in vitro selected RNA aptamers into in vivo functional riboswitches represents a long-standing challenge in molecular biology. The highly specific aptamer domain of the riboswitch undergoes a conformational adjustment in response to ligand sensing, which in turn exerts the regulatory function. Besides essential factors like structural complexity and ligand binding kinetics, the active role of magnesium ions in stabilizing RNA tertiary structures and assisting in ligand binding can be a vital criterion. We present spectroscopic studies on the magnesium ion-driven folding of the Tetracycline binding aptamer. Using fluorescent labels, the aptamer pre-folding and subsequent ligand binding is monitored by magnesium titration experiments and time-resolved stopped-flow measurements. A minimum concentration of 0.5 mM magnesium is required to fold into a magnesium ion-stabilized binding-competent state with a preformed binding pocket. Tetracycline binding causes a pronounced conformational change that results in the establishment of the triple helix core motif, and that further propagates towards the closing stem. By a dynamic acquisition of magnesium ions, a kink motif is formed at the intersection of the triple helix and closing stem regions. This ultimately entails a stabilization of the closing stem which is discussed as a key element in the regulatory function of the Tetracycline aptamer.

Typ des Eintrags: Artikel
Erschienen: 2023
Autor(en): Kaiser, Christoph ; Vogel, Marc ; Appel, Bettina ; Weigand, Julia ; Müller, Sabine ; Suess, Beatrix ; Wachtveitl, Josef
Art des Eintrags: Bibliographie
Titel: Magnesium ion-driven folding and conformational switching kinetics of tetracycline binding aptamer: implications for in vivo riboswitch engineering
Sprache: Englisch
Publikationsjahr: 26 August 2023
Verlag: Elsevier
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Journal of molecular biology
Jahrgang/Volume einer Zeitschrift: 435
(Heft-)Nummer: 20
DOI: 10.1016/j.jmb.2023.168253
Kurzbeschreibung (Abstract):

Engineering in vitro selected RNA aptamers into in vivo functional riboswitches represents a long-standing challenge in molecular biology. The highly specific aptamer domain of the riboswitch undergoes a conformational adjustment in response to ligand sensing, which in turn exerts the regulatory function. Besides essential factors like structural complexity and ligand binding kinetics, the active role of magnesium ions in stabilizing RNA tertiary structures and assisting in ligand binding can be a vital criterion. We present spectroscopic studies on the magnesium ion-driven folding of the Tetracycline binding aptamer. Using fluorescent labels, the aptamer pre-folding and subsequent ligand binding is monitored by magnesium titration experiments and time-resolved stopped-flow measurements. A minimum concentration of 0.5 mM magnesium is required to fold into a magnesium ion-stabilized binding-competent state with a preformed binding pocket. Tetracycline binding causes a pronounced conformational change that results in the establishment of the triple helix core motif, and that further propagates towards the closing stem. By a dynamic acquisition of magnesium ions, a kink motif is formed at the intersection of the triple helix and closing stem regions. This ultimately entails a stabilization of the closing stem which is discussed as a key element in the regulatory function of the Tetracycline aptamer.

ID-Nummer: pmid:37640152
Zusätzliche Informationen:

Artikel-ID: 168253

Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie
10 Fachbereich Biologie > Synthetic RNA biology
Hinterlegungsdatum: 05 Sep 2023 06:46
Letzte Änderung: 11 Okt 2023 07:08
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