8qe4: Difference between revisions
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==Formation of left-handed helices by C2'-fluorinated nucleic acids under physiological salt conditions== | |||
<StructureSection load='8qe4' size='340' side='right'caption='[[8qe4]]' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[8qe4]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=8QE4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8QE4 FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</td></tr> | |||
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=GF2:2-DEOXY-2-FLUOROGUANOSINE+5-(DIHYDROGEN+PHOSPHATE)'>GF2</scene></td></tr> | |||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8qe4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8qe4 OCA], [https://pdbe.org/8qe4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8qe4 RCSB], [https://www.ebi.ac.uk/pdbsum/8qe4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8qe4 ProSAT]</span></td></tr> | |||
</table> | |||
<div style="background-color:#fffaf0;"> | |||
== Publication Abstract from PubMed == | |||
Recent findings in cell biology have rekindled interest in Z-DNA, the left-handed helical form of DNA. We report here that two minimally modified nucleosides, 2'F-araC and 2'F-riboG, induce the formation of the Z-form under low ionic strength. We show that oligomers entirely made of these two nucleosides exclusively produce left-handed duplexes that bind to the Zalpha domain of ADAR1. The effect of the two nucleotides is so dramatic that Z-form duplexes are the only species observed in 10 mM sodium phosphate buffer and neutral pH, and no B-form is observed at any temperature. Hence, in contrast to other studies reporting formation of Z/B-form equilibria by a preference for purine glycosidic angles in syn, our NMR and computational work revealed that sequential 2'F...H2N and intramolecular 3'H...N3' interactions stabilize the left-handed helix. The equilibrium between B- and Z- forms is slow in the 19F NMR time scale (>/=ms), and each conformation exhibited unprecedented chemical shift differences in the 19F signals. This observation led to a reliable estimation of the relative population of B and Z species and enabled us to monitor B-Z transitions under different conditions. The unique features of 2'F-modified DNA should thus be a valuable addition to existing techniques for specific detection of new Z-binding proteins and ligands. | |||
Formation of left-handed helices by C2'-fluorinated nucleic acids under physiological salt conditions.,El-Khoury R, Cabrero C, Movilla S, Kaur H, Friedland D, Dominguez A, Thorpe JD, Roman M, Orozco M, Gonzalez C, Damha MJ Nucleic Acids Res. 2024 Jul 22;52(13):7414-7428. doi: 10.1093/nar/gkae508. PMID:38874502<ref>PMID:38874502</ref> | |||
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |||
[[Category: | </div> | ||
<div class="pdbe-citations 8qe4" style="background-color:#fffaf0;"></div> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Large Structures]] | |||
[[Category: Synthetic construct]] | |||
[[Category: Cabrero C]] | |||
[[Category: Damha M]] | |||
[[Category: El-Khoury R]] | |||
[[Category: Friedland D]] | |||
[[Category: Gonzalez C]] | |||
[[Category: Movilla S]] | |||
[[Category: Orozco M]] | |||
[[Category: Roman M]] | |||
[[Category: Thorpe JD]] | |||
Latest revision as of 06:13, 31 July 2024
Formation of left-handed helices by C2'-fluorinated nucleic acids under physiological salt conditions
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