Bulletin of the American Physical Society
APS March Meeting 2020
Volume 65, Number 1
Monday–Friday, March 2–6, 2020; Denver, Colorado
Session G22: Biopolymers: Nucleic Acids and Structural
11:15 AM–1:39 PM,
Tuesday, March 3, 2020
Room: 303
Sponsoring
Units:
DBIO DSOFT
Chair: Ralf Bundschuh, Ohio State Univ - Columbus
Abstract: G22.00011 : Existence of the B-Form DNA helix in nanoDNA liquid crystals and its variation due to aggregate assembly*
View Presentation Abstract
Presenter:
Gregory Smith
(University of Colorado, Boulder)
Authors:
Gregory Smith
(University of Colorado, Boulder)
Tommaso Fraccia
(ESPCI Paris, Intitut Pierre-Gilles de Gennes)
Mikhail Zhernenkov
(NSLS-II, Brookhaven National Laboratory)
Tommaso Bellini
(University of Milan)
Noel Anthony Clark
(University of Colorado, Boulder)
We show using diffraction of a synchrotron X-ray microbeam that liquid crystalline aggregates of 12mer nanoDNA, such as the Drew-Dickerson Dodecamer (DD), demonstrate a B-form DNA double helix with a comparable degree of order to that seen in longer DNA, such as the calf-thymus DNA used by Rosalind Franklin to produce the historic Photo 51. This finding is significant because it shows that B-form helical order persists in liquid crystals of DD even though the backbone of the column contains a double-strand break at every twelfth position and the DD segments are not part of a full structured crystal. The coherence of the B-form helix is influenced by the mode of aggregate self-assembly, where aggregates assembled by a base-paired sticky-end produce much longer helical correlation lengths than those formed by hydrophobic blunt-ends. Finally, we found that aggregates of blunt-end 4mer oligomers shorter than half of a single B-form helical turn no longer display the B-form helical diffraction pattern but order with a different structure. This study gives fundamental insight into the extent to which the classical DNA helix is affected by discontinuity in the polymer backbone.
*
Funding provided by NSF MRSEC Grant DMR-1420736 and NSF Biomaterials Grant DMR-1611272.
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