The Sequence-Specific Cellular Uptake of Spherical Nucleic Acid Nanoparticle Conjugates
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AbstractThe sequence-dependent cellular uptake of spherical nucleic acid nanoparticle conjugates (SNAs) is investigated. This process occurs by interaction with class A scavenger receptors (SR-A) and caveolae-mediated endocytosis. It is known that linear poly(guanine) (poly G) is a natural ligand for SR-A, and it has been proposed that interaction of poly G with SR-A is dependent on the formation of G-quadruplexes. Since G-rich oligonucleotides are known to interact strongly with SR-A, it is hypothesized that SNAs with higher G contents would be able to enter cells in larger amounts than SNAs composed of other nucleotides, and as such, cellular internalization of SNAs is measured as a function of constituent oligonucleotide sequence. Indeed, SNAs with enriched G content show the highest cellular uptake. Using this hypothesis, a small molecule (camptothecin) is chemically conjugated with SNAs to create drug-SNA conjugates and it is observed that poly G SNAs deliver the most camptothecin to cells and have the highest cytotoxicity in cancer cells. Our data elucidate important design considerations for enhancing the intracellular delivery of spherical nucleic acids.
All Author(s) ListNarayan S.P., Choi C.H.J., Hao L., Calabrese C.M., Auyeung E., Zhang C., Goor O.J.G.M., Mirkin C.A.
Journal nameSmall
Detailed descriptionTo ORKTS: Suguna P. Narayan and I contributed equally to this work as co-first authors.
Year2015
Month9
Day1
Volume Number11
Issue Number33
PublisherWiley - V C H Verlag GmbbH & Co.
Place of PublicationGermany
Pages4173 - 4182
ISSN1613-6810
eISSN1613-6829
LanguagesEnglish-United Kingdom
Keywordscellular uptake, guanine, nanoparticles, sequence-specific, spherical nucleic acids

Last updated on 2020-26-09 at 02:51