Evidence map›Paper›PMID 35275940›Full record

ArticlePloS one2022

Close correlation between thiolate basicity and certain NMR parameters in cysteine and cystine microspecies.

Juliana Ferreira de Santana, Arash Mirzahosseini, Beáta Mándity, Dóra Bogdán, István Mándity, Béla Noszál

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.9field-weighted citation impact, top 28% 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

2 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. 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

6 authors at 2 institutions in 1 country.

Juliana Ferreira de SantanaDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest, Hungary.
Arash MirzahosseiniDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest, Hungary.
Beáta MándityMTA TTK Lendület Artificial Transporter Research Group, Institute of Materials and Environmental Chemistry, Research Center for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Dóra BogdánMTA TTK Lendület Artificial Transporter Research Group, Institute of Materials and Environmental Chemistry, Research Center for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
István MándityMTA TTK Lendület Artificial Transporter Research Group, Institute of Materials and Environmental Chemistry, Research Center for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary.
Béla NoszálDepartment of Pharmaceutical Chemistry, Semmelweis University, Budapest, Hungary.ORCID 0000-0003-3898-3084
Semmelweis University · HUInstitute of Materials and Environmental Chemistry · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The imbalance between prooxidants and antioxidants in biological systems, known as oxidative stress, can lead to a disruption of redox signaling by the reactive oxygen/nitrogen species and is related to severe diseases. The most vulnerable moiety targeted by oxidant species in the redox signaling pathways is the thiol (SH) group in the cysteine residues, especially in its deprotonated (S-) form. Cysteine, along with its oxidized, disulfide-containing form, cystine, constitute one of the most abundant low molecular weight biological redox couples, providing a significant contribution to the redox homeostasis in living systems. In this work, NMR spectra from cysteine, cystine, and cysteine-containing small peptides were thoroughly studied at the submolecular level, and through the chemical shift data set of their certain atoms it is possible to estimate either thiolate basicity or the also related standard redox potential. Regression analysis demonstrated a strong linear relationship for chemical shift vs thiolate logK of the cysteine microspecies data. The αCH 13C chemical shift is the most promising estimator of the acid-base and redox character.

Indexed as

CysteineCystineGlutathioneOxidation-ReductionReactive Nitrogen SpeciesReactive Oxygen SpeciesSulfhydryl CompoundsCysteineCystineGlutathioneReactive Nitrogen SpeciesReactive Oxygen SpeciesSulfhydryl Compounds

Identifiers

PMID35275940
PMCPMC8916652
OpenAlexW4220964357

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.