Evidence map›Paper›PMID 35102310›Full record

ReviewNature protocols2022

High-resolution imaging of bacterial spatial organization with vertical cell imaging by nanostructured immobilization (VerCINI).

Kevin D Whitley, Stuart Middlemiss, Calum Jukes, Cees Dekker, Séamus Holden

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Article
  2. Review
  3. Journal of bacteriology · 2025
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Kevin D WhitleyCentre for Bacterial Cell Biology, Biosciences Insitute, Newcastle University, Newcastle upon Tyne, UK. kevin.whitley@ncl.ac.uk.ORCID http://orcid.org/0000-0001-9719-6916
Stuart MiddlemissCentre for Bacterial Cell Biology, Biosciences Insitute, Newcastle University, Newcastle upon Tyne, UK.
Calum JukesCentre for Bacterial Cell Biology, Biosciences Insitute, Newcastle University, Newcastle upon Tyne, UK.
Cees DekkerDepartment of Bionanoscience, Kavli Institute of Nanoscience Delft, Delft University of Technology, Delft, the Netherlands.ORCID http://orcid.org/0000-0001-6273-071X
Séamus HoldenCentre for Bacterial Cell Biology, Biosciences Insitute, Newcastle University, Newcastle upon Tyne, UK. seamus.holden@ncl.ac.uk.ORCID http://orcid.org/0000-0002-7169-907X

Funding

Biotechnology and Biological Sciences Research CouncilWellcome Trust (Wellcome) 206670/Z/17/Z
6 · The paper itself

Abstract

Light microscopy is indispensable for analysis of bacterial spatial organization, yet the sizes and shapes of bacterial cells pose unique challenges to imaging. Bacterial cells are not much larger than the diffraction limit of visible light, and many species have cylindrical shapes and so lie flat on microscope coverslips, yielding low-resolution images when observing their short axes. In this protocol, we describe a pair of recently developed methods named VerCINI (vertical cell imaging by nanostructured immobilization) and µVerCINI (microfluidic VerCINI) that greatly increase spatial resolution and image quality for microscopy of the short axes of bacteria. The concept behind both methods is that cells are imaged while confined vertically inside cell traps made from a nanofabricated mold. The mold is a patterned silicon wafer produced in a cleanroom facility using electron-beam lithography and deep reactive ion etching, which takes ~3 h for fabrication and ~12 h for surface passivation. After obtaining a mold, the entire process of making cell traps, imaging cells and processing images can take ~2-12 h, depending on the experiment. VerCINI and µVerCINI are ideal for imaging any process along the short axes of bacterial cells, as they provide high-resolution images without any special requirements for fluorophores or imaging modalities, and can readily be combined with other imaging methods (e.g., STORM). VerCINI can easily be incorporated into existing projects by researchers with expertise in bacteriology and microscopy. Nanofabrication can be either done in-house, requiring specialist facilities, or outsourced based on this protocol.

Indexed as

MicroscopyNanostructuresBacteriaFluorescent DyesSiliconFluorescent DyesSilicon

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.