Evidence map›Paper›PMID 34067755›Full record

ArticleInternational journal of molecular sciences2021

Soluble Prokaryotic Overexpression and Purification of Human GM-CSF Using the Protein Disulfide Isomerase b'a' Domain.

Thi Kieu Oanh Nguyen, Thi Luong Vu, Minh Quan Nguyen, Huynh Kim Khanh Ta, Kyoung Sun Park, Soo Hyeon Kim, Chong Jai Kim, Yeon Jin Jang, Han Choe

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-weighted citation impact, top 40% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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

9 authors at 2 institutions in 1 country.

Thi Kieu Oanh NguyenDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.ORCID 0000-0001-6299-0191
Thi Luong VuDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.
Minh Quan NguyenDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.
Huynh Kim Khanh TaDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.
Kyoung Sun ParkWide River Institute of Immunology, Seoul National University College of Medicine, Seoul 25159, Korea.
Soo Hyeon KimWide River Institute of Immunology, Seoul National University College of Medicine, Seoul 25159, Korea.
Chong Jai KimDepartment of Pathology, Asan-Minnesota Institute for Innovating Transplantation, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.
Yeon Jin JangDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.ORCID 0000-0001-7350-5534
Han ChoeDepartment of Physiology, Bio-Medical Institute of Technology, University of Ulsan College of Medicine, Asan Medical Center, Seoul 05505, Korea.ORCID 0000-0003-4604-647X
Ulsan College · KRSeoul National University · KR

Funding

Asan Institute for Life Sciences, Seoul, Korea 2018-IL0307-01National Research Foundation of Korea NRF-2015K1A4A3046807 and NRF-2020R1F1A1075651
6 · The paper itself

Abstract

Granulocyte-macrophage colony-stimulating factor (GM-CSF) is a member of the colony-stimulating factor (CSF) family, which functions to enhance the proliferation and differentiation of hematopoietic stem cells and other hematopoietic lineages such as neutrophils, dendritic cells, or macrophages. These proteins have thus generated considerable interest in clinical therapy research. A current obstacle to the prokaryotic production of human GM-CSF (hGM-CSF) is its low solubility when overexpressed and subsequent complex refolding processes. In our present study, the solubility of hGM-CSF was examined when combined with three N-terminal fusion tags in five

Indexed as

Cell DifferentiationChromatography, GelElectrophoresis, Polyacrylamide GelGranulocyte-Macrophage Colony-Stimulating FactorHematopoietic Stem CellsHumansMaltose-Binding ProteinsProkaryotic CellsProtein Disulfide-IsomerasesProtein TransportSolubilityCSF2 protein, humanGranulocyte-Macrophage Colony-Stimulating FactorMaltose-Binding ProteinsProtein Disulfide-IsomerasesClearColihGM-CSFMBPPDI

Identifiers

PMID34067755
PMCPMC8156066
OpenAlexW3161035083

What OpenQuestion holds

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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.