Evidence map›Paper›PMID 32884863›Full record

ArticlePeerJ2020

Human granulocyte-colony stimulating factor (G-CSF)/stem cell factor (SCF) fusion proteins: design, characterization and activity.

Gitana Mickiene, Indrė Dalgėdienė, Gintautas Zvirblis, Zilvinas Dapkunas, Ieva Plikusiene, Ernesta Buzavaite-Verteliene, Zigmas Balevičius, Audronė Rukšėnaitė, Milda Pleckaityte

Open access · goldAbstract read
In one paragraph

Article in PeerJ, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 36% 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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. Article
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

9 authors at 2 institutions in 1 country.

Gitana MickieneInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.
Indrė DalgėdienėInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.ORCID 0000-0003-4113-4761
Gintautas ZvirblisInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.
Zilvinas DapkunasInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.
Ieva PlikusieneDepartment of Physical Chemistry, Faculty of Chemistry and Geosciences, Vilnius University, Vilnius, Lithuania.
Ernesta Buzavaite-VertelienePlasmonics and Nanophotonics Laboratory, Department of Laser Technology, Center for Physical Sciences and Technology, Vilnius, Lithuania.
Zigmas BalevičiusPlasmonics and Nanophotonics Laboratory, Department of Laser Technology, Center for Physical Sciences and Technology, Vilnius, Lithuania.
Audronė RukšėnaitėInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.
Milda PleckaityteInstitute of Biotechnology, Vilnius University, Vilnius, Lithuania.
Vilnius University · LTCenter for Physical Sciences and Technology · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundStem cell factor (SCF) and granulocyte-colony stimulating factor (G-CSF) are well-characterized vital hematopoietic growth factors that regulate hematopoiesis. G-CSF and SCF synergistically exhibit a stimulatory effect on hematopoietic progenitors. The combination of G-CSF and SCF has been used for mobilization of peripheral blood progenitor cells in cancer and non-cancerous conditions. To overcome challenges connected with the administration of two cytokines, we developed two fusion proteins composed of human SCF and human G-CSF interspaced by an alpha-helix-forming peptide linker.

methodsThe recombinant proteins SCF-Lα-GCSF and GCSF-Lα-SCF were purified in three steps using an ion-exchange and mixed-mode chromatography. The purity and quantity of the proteins after each stage of purification was assessed using RP-HPLC, SDS-PAGE, and the Bradford assays. Purified proteins were identified using high-performance liquid chromatography/electrospray ionization mass spectrometry (HPLC/ESI-MS) and the Western blot analyses. The molecular weight was determined by size exclusion HPLC (SE-HPLC). The activity of heterodimers was assessed using cell proliferation assays in vitro. The capacity of recombinant fusion proteins to stimulate the increase of the absolute neutrophil count in rats was determined in vivo. The binding kinetics of the proteins to immobilized G-CSF and SCF receptors was measured using total internal reflection ellipsometry and evaluated by a standard Langmuir kinetics model.

resultsThe novel SCF-Lα-GCSF and GCSF-Lα-SCF proteins were synthesized in

Indexed as

Absolute neutrophil countActivityCytokinesFusion proteinsG-CSFHematopoiesisLinkerProtein purificationSCF

Identifiers

PMID32884863
PMCPMC7444511
OpenAlexW3080547598

What OpenQuestion holds

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LicenceCC BY
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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.