TY - JOUR
T1 - Programmable Matter
T2 - The Nanoparticle Atom and DNA Bond
AU - Samanta, Devleena
AU - Zhou, Wenjie
AU - Ebrahimi, Sasha B.
AU - Petrosko, Sarah Hurst
AU - Mirkin, Chad A.
N1 - Funding Information:
This article is part of the Advanced Materials Hall of Fame article series, which recognizes the excellent contributions of leading researchers to the field of materials science. This material is based upon work supported by the Air Force Office of Scientific Research award FA9550‐17‐1‐0348 (colloidal crystallization) and as part of the Center for Bio‐Inspired Energy Science, an Energy Frontier Research Center funded by the U.S. Department of Energy, Office of Science, Basic Energy Sciences under Award # DE‐SC0000989 (responsive DNA bonds).
Publisher Copyright:
© 2022 Wiley-VCH GmbH.
PY - 2022/3/24
Y1 - 2022/3/24
N2 - Colloidal crystal engineering with DNA has led to significant advances in bottom-up materials synthesis and a new way of thinking about fundamental concepts in chemistry. Here, programmable atom equivalents (PAEs), comprised of nanoparticles (the “atoms”) functionalized with DNA (the “bonding elements”), are assembled through DNA hybridization into crystalline lattices. Unlike atomic systems, the “atom” (e.g., the nanoparticle shape, size, and composition) and the “bond” (e.g., the DNA length and sequence) can be tuned independently, yielding designer materials with unique catalytic, optical, and biological properties. In this review, nearly three decades of work that have contributed to the evolution of this class of programmable matter is chronicled, starting from the earliest examples based on gold-core PAEs, and then delineating how advances in synthetic capabilities, DNA design, and fundamental understanding of PAE-PAE interactions have led to new classes of functional materials that, in several cases, have no natural equivalent.
AB - Colloidal crystal engineering with DNA has led to significant advances in bottom-up materials synthesis and a new way of thinking about fundamental concepts in chemistry. Here, programmable atom equivalents (PAEs), comprised of nanoparticles (the “atoms”) functionalized with DNA (the “bonding elements”), are assembled through DNA hybridization into crystalline lattices. Unlike atomic systems, the “atom” (e.g., the nanoparticle shape, size, and composition) and the “bond” (e.g., the DNA length and sequence) can be tuned independently, yielding designer materials with unique catalytic, optical, and biological properties. In this review, nearly three decades of work that have contributed to the evolution of this class of programmable matter is chronicled, starting from the earliest examples based on gold-core PAEs, and then delineating how advances in synthetic capabilities, DNA design, and fundamental understanding of PAE-PAE interactions have led to new classes of functional materials that, in several cases, have no natural equivalent.
KW - DNA
KW - colloidal crystal engineering
KW - nanoparticles
KW - programmable atom equivalent
KW - spherical nucleic acids
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U2 - 10.1002/adma.202107875
DO - 10.1002/adma.202107875
M3 - Review article
C2 - 34870875
AN - SCOPUS:85124494894
SN - 0935-9648
VL - 34
JO - Advanced Materials
JF - Advanced Materials
IS - 12
M1 - 2107875
ER -