| Literature DB >> 28088861 |
Matz Liebel1, James T Hugall1, Niek F van Hulst1,2.
Abstract
Label-free detection, analysis, and rapid tracking of nanoparticles is crucial for future ultrasensitive sensing applications, ranging from understanding of biological interactions to the study of size-dependent classical-quantum transitions. Yet optical techniques to distinguish nanoparticles directly among their background remain challenging. Here we present amplified interferometric scattering microscopy (a-iSCAT) as a new all-optical method capable of detecting individual nanoparticles as small as 15 kDa proteins that is equivalent to half a GFP. By balancing scattering and reflection amplitudes the interference contrast of the nanoparticle signal is amplified 1 to 2 orders of magnitude. Beyond high sensitivity, a-iSCAT allows high-speed image acquisition exceeding several hundreds of frames-per-second. We showcase the performance of our approach by detecting single Streptavidin binding events and by tracking single Ferritin proteins at 400 frames-per-second with 12 nm localization precision over seconds. Moreover, due to its extremely simple experimental realization, this advancement finally enables a cheap and routine implementation of label-free all-optical single nanoparticle detection platforms with sensitivity operating at the single protein level.Keywords: Interferometric scattering; balanced interference; digital holography; iSCAT; interference microscopy; label-free; single particle tracking; single-molecule detection; superresolution
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Year: 2017 PMID: 28088861 DOI: 10.1021/acs.nanolett.6b05040
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189