Paper detail

Multiplexed plasmonic nanoantennas for high throughput single molecule nanoscale dynamics in living cells

Single molecule detection has revolutionised the fields of chemistry and biology by offering powerful ways to study individual molecules under different scenarios. Nanophotonic structures, including plasmonic antennas, significantly overcome the concentration limit at which single molecule events can be observed, enabling their detection at concentrations that are relevant to biological and chemical processes. Although antennas can be fabricated in large arrays, probing dynamic events requires high temporal resolution, which is best achieved by serial antenna interrogation. Unfortunately, this precludes the simultaneous recording from multiple antennas at different sample locations, and is time consuming, resulting in poor statistics and low-throughput data acquisition, abating the true potential of arrays. Here we exploit arrays of antenna-in-box nanostructures in combination with sCMOS readout to interrogate nanoscale volumes from 225 antennas simultaneously. Recording at 1 kHz allowed multiplexed dynamic measurements from 50 nanoantennas simultaneously with a temporal resolution dictated by the camera framerate and the photons emitted per molecule during a single passage. We demonstrate the capability for high-throughput arrayed detection of single molecule dynamics at the nanoscale in the membrane of living cells, and determine the axial location of membrane molecular components with 1 nm accuracy and temporal resolution below 1 ms.

preprint2022arXivOpen access

Signal facts

What is known right now

Open access4 authors2 topics

Next steps

Decide what to do with this paper

Use like or dislike for the fast social read. The more specific scholarly feedback stays available below when needed.

Log in to curate

Reading frame

Keep the important context close to the paper

Keep the important signals around this paper in one place: votes, save state, collection context, reviews and the metadata you need before deciding what to do next.

Institutions

Add specific reaction

Move through the context

Research map

Open full explorer

Move through nearby people, institutions, topics and adjacent work without leaving the paper page.

Building this map preview

BZPEER is loading the nearby papers, people, topics and institutions for this page.

Structured reviews

0 review(s)

ContributeLeave structured feedbackUse the review template when you have a concrete strength, concern or method question.Open review form

No structured reviews yet. High-signal critique starts here.

Work discussion

0 comment(s)

DiscussAdd a high-signal commentKeep quick notes, caveats and replication pointers separate from formal reviews.Open comment form

No discussion yet. The first strong comment sets the tone.