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Self-Replicating DNA-Based Nanoassemblies

delete2024-06-25
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PRE
AI
N
Nahida Akter
B
B. Safeenaz Alladin‐Mustan
Y
Yuning Liu
J
Jisu An
J
Julianne M. Gibbs *
DOI:10.1021/jacs.4c04089delete
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摘要

摘要

En 中文
The properties of DNA that make it an effective genetic material also allow it to be ideal for programmed self-assembly. Such DNA-programmed assembly has been utilized to construct responsive DNA origami and wireframe nanoassemblies, yet replicating these hybrid nanomaterials remains challenging. Here we report a strategy for replicating DNA wireframe nanoassemblies using the isothermal ligase chain reaction lesion-induced DNA amplification (LIDA). We designed a triangle wireframe structure that can be formed in one step by ring-closing of its linear analog. Introducing a small amount of the wireframe triangle to an excess of the linear analog and complementary fragments, one of which contains a destabilizing abasic lesion, leads to rapid, sigmoidal self-replication of the wireframe triangle via cross-catalysis. Using the same cross-catalytic strategy we also demonstrate rapid self-replication of a hybrid wireframe triangle containing synthetic vertices as well as the self-replication of circular DNA. This work reveals the suitability of isothermal ligase chain reactions such as LIDA to self-replicate complex DNA architectures, opening the door to incorporating self-replication, a hallmark of life, into biomimetic DNA nanotechnology.
Keyword:
ROLLING-CIRCLE AMPLIFICATION
STABILITY
NANOSTRUCTURES
NANOTUBES
GEOMETRY

期刊

Journal of the American Chemical Society 封面图
Journal of the American Chemical Society
IF:
15.6
论文数:
20.0W
被引数:
60.2W

机构

U
university of alberta
学者数:
5.1W
论文数: 4.9W
被引数: 65
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