Evidence map›Paper›PMID 38162388›Full record

ArticleNature photonics2023

Bond-selective fluorescence imaging with single-molecule sensitivity.

Haomin Wang, Dongkwan Lee, Yulu Cao, Xiaotian Bi, Jiajun Du, Kun Miao, Lu Wei

Abstract read
In one paragraph

Article in Nature photonics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. The Fantastic Single-Molecule Techniques.Chemical & biomedical imaging · 2026
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Single-Molecule Vibrational Thermometry.The journal of physical chemistry. B · 2025
    Article
  12. Article
  13. Review
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Article
  20. Review
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

7 authors.

Haomin WangDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Dongkwan LeeDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Yulu CaoDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Xiaotian BiDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Jiajun DuDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Kun MiaoDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.
Lu WeiDivision of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.

Funding

Super-resolution Chemical Imaging for BiomedicineDP2GM140919 · NIGMS · CALIFORNIA INSTITUTE OF TECHNOLOGY · PI WEI, LU · 2020 to 2020
$2.3M
NIGMS NIH HHS DP2 GM140919
6 · The paper itself

Abstract

Bioimaging harnessing optical contrasts and chemical specificity is of vital importance in probing complex biology. Vibrational spectroscopy based on mid-infrared (mid-IR) excitation can reveal rich chemical information about molecular distributions. However, its full potential for bioimaging is hindered by the achievable sensitivity. Here, we report bond selective fluorescence-detected infrared-excited (BonFIRE) spectral microscopy. BonFIRE employs two-photon excitation in the mid-IR and near-IR to upconvert vibrational excitations to electronic states for fluorescence detection, thus encoding vibrational information into fluorescence. The system utilizes tuneable narrowband picosecond pulses to ensure high sensitivity, biocompatibility, and robustness for bond-selective biological interrogations over a wide spectrum of reporter molecules. We demonstrate BonFIRE spectral imaging in both fingerprint and cell-silent spectroscopic windows with single-molecule sensitivity for common fluorescent dyes. We then demonstrate BonFIRE imaging on various intracellular targets in fixed and live cells, neurons, and tissues, with promises for further vibrational multiplexing. For dynamic bioanalysis in living systems, we implement a high-frequency modulation scheme and demonstrate time-lapse BonFIRE microscopy of live HeLa cells. We expect BonFIRE to expand the bioimaging toolbox by providing a new level of bond-specific vibrational information and facilitate functional imaging and sensing for biological investigations.

Identifiers

PMID38162388
PMCPMC10756635

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Registered trials

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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.