
Protein Spherical Nucleic Acids for Live-Cell Chemical Analysis
Author(s) -
Devleena Samanta,
Sasha Ebrahimi,
Caroline D. Kusmierz,
Ho Fung Cheng,
Chad A. Mirkin
Publication year - 2020
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.0c06866
Subject(s) - chemistry , nucleic acid , glucose oxidase , fluorophore , analyte , biomolecule , biochemistry , nucleic acid quantitation , fluorescence , combinatorial chemistry , biophysics , biosensor , chromatography , physics , quantum mechanics , biology
We report the development of a new strategy for the chemical analysis of live cells based on protein spherical nucleic acids (ProSNAs). The ProSNA architecture enables analyte detection via the highly programmable nucleic acid shell or a functional protein core. As a proof-of-concept, we use an i-motif as the nucleic acid recognition element to probe pH in living cells. By interfacing the i-motif with a forced-intercalation readout, we introduce a quencher-free approach that is resistant to false-positive signals, overcoming limitations associated with conventional fluorophore/quencher-based gold NanoFlares. Using glucose oxidase as a functional protein core, we show activity-based, amplified sensing of glucose. This enzymatic system affords greater than 100-fold fluorescence turn on in buffer, is selective for glucose in the presence of close analogs (i.e., glucose-6-phosphate), and can detect glucose above a threshold concentration of ∼5 μM, which enables the study of relative changes in intracellular glucose concentrations.