Evidence map›Paper›PMID 40339779›Full record

ArticleAnalytical biochemistry2025

Double alkylation with maleimide-PEG-biotin: An enrichment method for cysteine redox states.

Jung Mi Lim, Rodney L Levine

Abstract read
In one paragraph

Article in Analytical biochemistry, 2025. 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

2 authors.

Jung Mi LimLaboratory of Biochemistry, National Heart, Lung, and Blood Institute, Building 50, Room 2347, 50 South Drive, MSC 8012, Bethesda, 20892-8012, Maryland, USA. Electronic address: jungmi.lim@nih.gov.
Rodney L LevineLaboratory of Biochemistry, National Heart, Lung, and Blood Institute, Building 50, Room 2351, 50 South Drive, MSC 8012, Bethesda, 20892-8012, Maryland, USA. Electronic address: rlevine@nih.gov.

Funding

Oxidative Modification Of ProteinsZIAHL000225 · NHLBI · NATIONAL HEART, LUNG, AND BLOOD INSTITUTE · PI LEVINE, RODNEY L. · 2009 to 2025
$35.2M
Intramural NIH HHS ZIA HL000225
6 · The paper itself

Abstract

Cysteine alkylation is widely used in mass-spectrometric based proteomic studies. The oxidation state of each cysteine can be determined by labeling free thiols with one alkylating agent and disulfides with a second alkylating agent that differs in mass from the first. We have developed an improved method utilizing biotin-conjugated maleimides to specifically label cysteine residues in the thiol state and in disulfide linkage. The biotin tag effectuates very efficient enrichment of cysteine containing peptides, greatly increasing sensitivity for those peptides. We also achieve very high recovery of the biotinylated peptides from an avidin column by elution with hexafluoro-2-propanol (HFIP). The method offers improved mapping of the cysteine proteome and its oxidation state.

Indexed as

BiotinCysteineMaleimidesPolyethylene GlycolsAlkylationOxidation-ReductionBiotinCysteinemaleimideMaleimidesPolyethylene Glycols

Identifiers

PMID40339779
PMCPMC12145231

What OpenQuestion holds

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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.