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DNA-Functionalized Metal–Organic Framework Nanoparticles for Intracellular Delivery of Proteins
Author(s) -
Shunzhi Wang,
Yijing Chen,
Shuya Wang,
Peng Li,
Chad A. Mirkin,
Omar K. Farha
Publication year - 2019
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/jacs.8b12705
Subject(s) - chemistry , oligonucleotide , nucleic acid , transfection , scavenger receptor , intracellular , nanoparticle , dna , biophysics , cell , nanotechnology , drug delivery , combinatorial chemistry , biochemistry , gene , lipoprotein , materials science , cholesterol , biology , organic chemistry
Due to their large size, charged surfaces, and environmental sensitivity, proteins do not naturally cross cell-membranes in intact form and, therefore, are difficult to deliver for both diagnostic and therapeutic purposes. Based upon the observation that clustered oligonucleotides can naturally engage scavenger receptors that facilitate cellular transfection, nucleic acid-metal organic framework nanoparticle (MOF NP) conjugates have been designed and synthesized from NU-1000 and PCN-222/MOF-545, respectively, and phosphate-terminated oligonucleotides. They have been characterized structurally and with respect to their ability to enter mammalian cells. The MOFs act as protein hosts, and their densely functionalized, oligonucleotide-rich surfaces make them colloidally stable and ensure facile cellular entry. With insulin as a model protein, high loading and a 10-fold enhancement of cellular uptake (as compared to that of the native protein) were achieved. Importantly, this approach can be generalized to facilitate the delivery of a variety of proteins as biological probes or potential therapeutics.

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