Evidence map›Paper›PMID 34168837›Full record

ArticleChemical science2021

Evaluation of fully-functionalized diazirine tags for chemical proteomic applications.

Louis P Conway, Appaso M Jadhav, Rick A Homan, Weichao Li, Juanita Sanchez Rubiano, Richard Hawkins, R Michael Lawrence, Christopher G Parker

Open access · diamondAbstract read
In one paragraph

Article in Chemical science, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
7.0field-weighted citation impact, top 2% of its field
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

35 citing papers in PubMed, 83 citations in OpenAlex.

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  8. Target Agnostic Photoaffinity Labelling by Sulfonylhydrazones.Angewandte Chemie (International ed. in English) · 2025
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  10. Synthetic Lipid Biology.Chemical reviews · 2025
    Review
  11. Light-Activated Reactivity of Nitrones with Amino Acids and Proteins.Angewandte Chemie (International ed. in English) · 2025
    Article
  12. Review
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  14. Article
  15. Article
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  17. Article
  18. Review
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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

8 authors at 2 institutions in 2 countries.

Louis P ConwayDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.
Appaso M JadhavDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.ORCID https://orcid.org/0000-0002-4892-0792
Rick A HomanDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.
Weichao LiDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.
Juanita Sanchez RubianoDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.
Richard HawkinsDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.ORCID https://orcid.org/0000-0002-7481-5419
R Michael LawrenceResearch and Development, Bristol Myers Squibb Company Princeton NJ USA.
Christopher G ParkerDepartment of Chemistry, The Scripps Research Institute Jupiter FL USA cparker@scripps.edu.ORCID https://orcid.org/0000-0001-8509-9289
Scripps Research Institute · USBristol-Myers Squibb (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The use of photo-affinity reagents for the mapping of noncovalent small molecule-protein interactions has become widespread. Recently, several 'fully-functionalized' (FF) chemical tags have been developed wherein a photoactivatable capture group, an enrichment handle, and a functional group for synthetic conjugation to a molecule of interest are integrated into a single modular tag. Diazirine-based FF tags in particular are increasingly employed in chemical proteomic investigations; however, despite routine usage, their relative utility has not been established. Here, we systematically evaluate several diazirine-containing FF tags, including a terminal diazirine analog developed herein, for chemical proteomic investigations. Specifically, we compared the general reactivity of five diazirine tags and assessed their impact on the profiles of various small molecules, including fragments and known inhibitors revealing that such tags can have profound effects on the proteomic profiles of chemical probes. Our findings should be informative for chemical probe design, photo-affinity reagent development, and chemical proteomic investigations.

Identifiers

PMID34168837
PMCPMC8188597
OpenAlexW3163343314

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LicenceCC BY
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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.