Reconstructing Sub-Cellular Structure with Plasmonic Metamaterials The ability to resolve intracellular structure has opened new opportunities for deciphering complex chemical interactions, for relating the composition and organization of organelles to cellular processes, and for observing the infection of cells by viruses. This project describes how plasmonic metamaterials can resolve sub-cellular structure in three dimensions (3D), with sub-diffraction resolution, and without the use of fluorescent labels. These new types of metal nanostructures can be integrated with standard optical microscopes. Because the light that emerges from a metal film perforated with a finite number of nanoholes (a patch) is periodically modulated in 3D, these plasmonic metamaterials can be used for determining the structure of thick, transparent samples like cells. Unlike in conventional optics, where lenses are situated far from the object, these planar metallic lens structures can be constructed directly on glass coverslips. Hence, higher resolution can be achieved because the light does not disperse prior to or after impinging on the sample. We propose to investigate two classes of plasmonic structures for the label-free imaging of cells: (1) gold films perforated with microscale patches of nanoscale holes, which can achieve 3D imaging by deconstructing interference patterns from structured beams of light and (2) gold pyramidal particles, which can be used to identify the spatial locations of specific biomarkers within cells.

Agency
National Institute of Health (NIH)
Institute
Office of The Director, National Institutes of Health (OD)
Type
NIH Director’s Pioneer Award (NDPA) (DP1)
Project #
5DP1OD003899-04
Application #
8134816
Study Section
Special Emphasis Panel (ZGM1-NDPA-B (P2))
Program Officer
Wehrle, Janna P
Project Start
2008-09-30
Project End
2012-07-31
Budget Start
2011-08-01
Budget End
2012-07-31
Support Year
4
Fiscal Year
2011
Total Cost
$754,875
Indirect Cost
Name
Northwestern University at Chicago
Department
Chemistry
Type
Schools of Arts and Sciences
DUNS #
160079455
City
Evanston
State
IL
Country
United States
Zip Code
60201
Rotz, Matthew W; Holbrook, Robert J; MacRenaris, Keith W et al. (2018) A Markedly Improved Synthetic Approach for the Preparation of Multifunctional Au-DNA Nanoparticle Conjugates Modified with Optical and MR Imaging Probes. Bioconjug Chem 29:3544-3549
Rotz, Matthew W; Culver, Kayla S B; Parigi, Giacomo et al. (2015) High relaxivity Gd(III)-DNA gold nanostars: investigation of shape effects on proton relaxation. ACS Nano 9:3385-96
Dam, Duncan Hieu M; Culver, Kayla S B; Kandela, Irawati et al. (2015) Biodistribution and in vivo toxicity of aptamer-loaded gold nanostars. Nanomedicine 11:671-9
Dam, Duncan Hieu M; Culver, Kayla S B; Odom, Teri W (2014) Grafting aptamers onto gold nanostars increases in vitro efficacy in a wide range of cancer cell types. Mol Pharm 11:580-7
Dam, Duncan Hieu M; Lee, Raymond C; Odom, Teri W (2014) Improved in vitro efficacy of gold nanoconstructs by increased loading of G-quadruplex aptamer. Nano Lett 14:2843-8
Hua, Yi; Suh, Jae Yong; Zhou, Wei et al. (2012) Talbot effect beyond the paraxial limit at optical frequencies. Opt Express 20:14284-91
Dam, Duncan Hieu M; Lee, Jung Heon; Sisco, Patrick N et al. (2012) Direct observation of nanoparticle-cancer cell nucleus interactions. ACS Nano 6:3318-26
Dam, Duncan Hieu M; Culver, Kayla S B; Sisco, Patrick N et al. (2012) Shining light on nuclear-targeted therapy using gold nanostar constructs. Ther Deliv 3:1263-7
Suh, Jae Yong; Huntington, Mark D; Kim, Chul Hoon et al. (2012) Extraordinary nonlinear absorption in 3D bowtie nanoantennas. Nano Lett 12:269-74
Stoerzinger, Kelsey A; Lin, Julia Y; Odom, Teri W (2011) Nanoparticle SERS substrates with 3D Raman-active volumes. Chem Sci 2:1435-1439

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