Comprehensive view of microscopic interactions between DNA-coated colloids.

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Abstrakt

Tytuł:: Comprehensive view of microscopic interactions between DNA-coated colloids.
Autorzy:: Cui F; Department of Physics, New York University, New York, NY, USA.
Marbach S; Courant Institute of Mathematical Sciences, New York University, New York, NY, USA.; CNRS, Sorbonne Université, Physicochimie des Electrolytes et Nanosystèmes, Interfaciaux, F-75005, Paris, France.
Zheng JA; Department of Physics, New York University, New York, NY, USA.
Holmes-Cerfon M; Courant Institute of Mathematical Sciences, New York University, New York, NY, USA.
Pine DJ; Department of Physics, New York University, New York, NY, USA. .; Department of Chemical & Biomolecular Engineering, New York University, New York, NY, USA. .
Źródło:: Nature communications [Nat Commun] 2022 Apr 28; Vol. 13 (1), pp. 2304. Date of Electronic Publication: 2022 Apr 28.
Typ publikacji:: Journal Article; Research Support, U.S. Gov't, Non-P.H.S.; Research Support, Non-U.S. Gov't
Język:: English
Imprint Name(s):: Original Publication: [London] : Nature Pub. Group
MeSH Terms:: Colloids*/chemistry
DNA*/chemistry
Base Sequence ; Crystallization ; Nanotechnology
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Substance Nomenclature:: 0 (Colloids)
9007-49-2 (DNA)
Entry Date(s):: Date Created: 20220428 Date Completed: 20220502 Latest Revision: 20221112
Update Code:: 20240105
PubMed Central ID:: PMC9051097
DOI:: 10.1038/s41467-022-29853-w
PMID:: 35484104
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The self-assembly of DNA-coated colloids into highly-ordered structures offers great promise for advanced optical materials. However, control of disorder, defects, melting, and crystal growth is hindered by the lack of a microscopic understanding of DNA-mediated colloidal interactions. Here we use total internal reflection microscopy to measure in situ the interaction potential between DNA-coated colloids with nanometer resolution and the macroscopic melting behavior. The range and strength of the interaction are measured and linked to key material design parameters, including DNA sequence, polymer length, grafting density, and complementary fraction. We present a first-principles model that screens and combines existing theories into one coherent framework and quantitatively reproduces our experimental data without fitting parameters over a wide range of DNA ligand designs. Our theory identifies a subtle competition between DNA binding and steric repulsion and accurately predicts adhesion and melting at a molecular level. Combining experimental and theoretical results, our work provides a quantitative and predictive approach for guiding material design with DNA-nanotechnology and can be further extended to a diversity of colloidal and biological systems.
(© 2022. The Author(s).)

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