Hexagonal Plasmonic Arrays for High-Throughput Multicolor Single-Molecule Studies

被引:1
作者
Herkert, Ediz Kaan [1 ]
Lau, Lukas [1 ]
Pons Lanau, Roger [1 ]
Garcia-Parajo, Maria F. [1 ,2 ]
机构
[1] Barcelona Inst Sci & Technol, ICFO Inst Ciencies Foton, Barcelona 08860, Spain
[2] ICREA, E-08010 Barcelona, Spain
基金
欧盟地平线“2020”;
关键词
nanophotonic biosensors; single-molecule detection; multicolor fluorescence detection; high-throughput sensing; plasmonics; FLUORESCENCE CORRELATION SPECTROSCOPY; MODE WAVE-GUIDES; MEMBRANE; ALUMINUM; PLATFORM;
D O I
10.1021/acsami.4c04744
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Nanophotonic biosensors offer exceptional sensitivity in the presence of strong background signals by enhancing and confining light in subwavelength volumes. In the field of nanophotonic biosensors, antenna-in-box (AiB) designs consisting of a nanoantenna within a nanoaperture have demonstrated remarkable single-molecule fluorescence detection sensitivities under physiologically relevant conditions. However, their full potential has not yet been exploited as current designs prohibit insightful correlative multicolor single-molecule studies and are limited in terms of throughput. Here, we overcome these constraints by introducing aluminum-based hexagonal close-packed AiB (HCP-AiB) arrays. Our approach enables the parallel readout of over 1000 HCP-AiBs with multicolor single-molecule sensitivity up to micromolar concentrations using an alternating three-color excitation scheme and epi-fluorescence detection. Notably, the high-density HCP-AiB arrays not only enable high-throughput studies at micromolar concentrations but also offer high single-molecule detection probabilities in the nanomolar range. We demonstrate that robust and alignment-free correlative multicolor studies are possible using optical fiducial markers even when imaging in the low millisecond range. These advancements pave the way for the use of HCP-AiB arrays as biosensor architectures for high-throughput multicolor studies on single-molecule dynamics.
引用
收藏
页码:41271 / 41280
页数:10
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