Evidence map›Paper›PMID 37686361›Full record

ArticleInternational journal of molecular sciences2023

Changes in Hemoglobin Properties in Complex with Glutathione and after Glutathionylation.

Iuliia D Kuleshova, Pavel I Zaripov, Yuri M Poluektov, Anastasia A Anashkina, Dmitry N Kaluzhny, Evgeniia Yu Parshina, Georgy V Maksimov, Vladimir A Mitkevich, Alexander A Makarov, Irina Yu Petrushanko

Abstract read
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Article in International journal of molecular sciences, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

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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

7 citing papers in PubMed.

  1. Redox Potential (EMolecules (Basel, Switzerland) · 2025
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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

10 authors.

Iuliia D KuleshovaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0009-0006-4384-3907
Pavel I ZaripovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0003-1627-1350
Yuri M PoluektovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0002-9710-7490
Anastasia A AnashkinaEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.
Dmitry N KaluzhnyEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0001-7090-3334
Evgeniia Yu ParshinaFaculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.ORCID 0000-0001-7072-0693
Georgy V MaksimovFaculty of Biology, Lomonosov Moscow State University, Moscow 119234, Russia.ORCID 0000-0002-7377-0773
Vladimir A MitkevichEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0002-1517-1983
Alexander A MakarovEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.
Irina Yu PetrushankoEngelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow 119991, Russia.ORCID 0000-0003-0787-415X

Funding

Russian Science Foundation 19-14-00374
6 · The paper itself

Abstract

Hemoglobin is the main protein of red blood cells that provides oxygen transport to all cells of the human body. The ability of hemoglobin to bind the main low-molecular-weight thiol of the cell glutathione, both covalently and noncovalently, is not only an important part of the antioxidant protection of red blood cells, but also affects its affinity for oxygen in both cases. In this study, the properties of oxyhemoglobin in complex with reduced glutathione (GSH) and properties of glutathionylated hemoglobin bound to glutathione via an SS bond were characterized. For this purpose, the methods of circular dichroism, Raman spectroscopy, infrared spectroscopy, tryptophan fluorescence, differential scanning fluorimetry, and molecular modeling were used. It was found that the glutathionylation of oxyhemoglobin caused changes in the secondary structure of the protein, reducing the alpha helicity, but did not affect the heme environment, tryptophan fluorescence, and the thermostability of the protein. In the noncovalent complex of oxyhemoglobin with reduced glutathione, the secondary structure of hemoglobin remained almost unchanged; however, changes in the heme environment and the microenvironment of tryptophans, as well as a decrease in the protein's thermal stability, were observed. Thus, the formation of a noncovalent complex of hemoglobin with glutathione makes a more significant effect on the tertiary and quaternary structure of hemoglobin than glutathionylation, which mainly affects the secondary structure of the protein. The obtained data are important for understanding the functioning of glutathionylated hemoglobin, which is a marker of oxidative stress, and hemoglobin in complex with GSH, which appears to deposit GSH and release it during deoxygenation to increase the antioxidant protection of cells.

Indexed as

AntioxidantsOxyhemoglobinsGlutathioneHemeHemoglobinsHumansOxygenTryptophanAntioxidantsGlutathioneHemeHemoglobinsOxygenOxyhemoglobinsTryptophancircular dichroismdifferential scanning fluorometryglutathioneglutathionylationhemoglobininfrared spectroscopymolecular modelingRaman scatteringtryptophan fluorescence

Identifiers

PMID37686361
PMCPMC10487563

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