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Published September 2016 | Supplemental Material
Journal Article Open

Nanoparticle‐Templated Molecular Recognition Platforms for Detection of Biological Analytes

Abstract

Molecular recognition of biological analytes with optical nanosensors provides both spatial and temporal biochemical information. A recently developed sensing platform exploits near-infrared fluorescent single-wall carbon nanotubes combined with electrostatically pinned heteropolymers to yield a synthetic molecular recognition technique that is maximally transparent through biological matter. This molecular recognition technique is known as corona phase molecular recognition (CoPhMoRe). In CoPhMoRe, the specificity of a folded polymer toward an analyte does not arise from a pre-existing polymer-analyte chemical affinity. Rather, specificity is conferred through conformational changes undergone by a polymer that is pinned to the surface of a nanoparticle in the presence of an analyte and the subsequent modifications in fluorescence readout of the nanoparticles. The protocols in this article describe a novel single-molecule microscopy tool (near-infrared fluorescence and total internal reflection fluorescence [nIRF TIRF] hybrid microscope) to visualize the CoPhMoRe recognition process, enabling a better understanding of synthetic molecular recognition. We describe this requisite microscope for simultaneous single-molecule visualization of optical molecular recognition and signal transduction. We elaborate on the general procedures for synthesizing and identifying single-walled carbon nanotube-based sensors that employ CoPhMoRe via two biologically relevant examples of single-molecule recognition for the hormone estradiol and the neurotransmitter dopamine.

Additional Information

© 2016 John Wiley & Sons. Issue Online: 13 September 2016. Version of Record online: 13 September 2016. This work was supported by a Burroughs Wellcome Fund Career Award at the Scientific Interface (CASI), a Brain and Behavior Research foundation young investigator grant, and a Beckman Foundation Investigator Award. A.G.B. acknowledges a U.C. Berkeley Chancellor's Fellowship and an NSF Graduate Research Fellowship. G.S.D. acknowledges a Schlumberger Foundation Fellowship. A.G.B. wrote the introduction, Basic Protocols 1 and 2, and Support Protocols 1 and 2. G.S.D. wrote Basic Protocols 3 and 4, Support Protocols 3, 4, and 5, and commentary parts of this paper. A.G.B. and G.S.D. collaboratively edited the manuscript with guidance from M.P.L. The authors would like to thank Roger Chang for helpful discussions. Supporting Materials. All supporting material figure and text files discussed in this article can only be accessed from the online version of this article. Authors of this manuscript declare no conflicts of interest.

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