Evidence map›Paper›PMID 42275002›Full record

ArticleACS chemical biology2026

Stability-Based Proteomic Methods Add Value to Activity-Based Protein Profiling Studies.

You Zou, Diego J Sanson, Jianli Wu, Gibeom Nam, Ssu-Yu Chen, Jiyong Hong, Jen-Tsan Chi, Michael C Fitzgerald

Abstract read
In one paragraph

Article in ACS chemical biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

You ZouDepartment of Chemistry, Duke University, Durham, North Carolina 27708, United States.
Diego J SansonDepartment of Chemistry, Duke University, Durham, North Carolina 27708, United States.
Jianli WuDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, United States.
Gibeom NamDepartment of Chemistry, Duke University, Durham, North Carolina 27708, United States.ORCID 0009-0002-0587-2126
Ssu-Yu ChenDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, United States.
Jiyong HongDepartment of Chemistry, Duke University, Durham, North Carolina 27708, United States.ORCID 0000-0002-5253-0949
Jen-Tsan ChiDepartment of Molecular Genetics and Microbiology, Duke University Medical Center, Durham, North Carolina 27710, United States.
Michael C FitzgeraldDepartment of Chemistry, Duke University, Durham, North Carolina 27708, United States.ORCID 0000-0002-6719-4722

Funding

Noncovalent interaction of mutant KRAS inhibitorsR21CA297690 · NCI · DUKE UNIVERSITY · PI CHI, JEN-TSAN ASHLEY · 2025 to 2025
$411k
NCI NIH HHS R21 CA297690
6 · The paper itself

Abstract

Covalent inhibitors offer powerful therapeutic advantages over noncovalent inhibitors, but like noncovalent inhibitors, they require comprehensive profiling to define their on- and off-target activities. Here, we report on the use of two stability-based proteomic methods, stability of proteins from rates of oxidation (SPROX) and thermal protein profiling (TPP), to identify protein targets of covalent inhibitors using the KRAS

Indexed as

ProteomicsCell Line, TumorHumansProtein Stability

Identifiers

PMID42275002
PMCPMC13338933

What OpenQuestion holds

Textmetadata
LicenceTDM
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.