Evidence map›Paper›PMID 25450830›Full record

ArticleInternational journal of biological macromolecules2015

Two-step purification procedure for recombinant human asialoerythropoietin expressed in transgenic plants.

Farooqahmed S Kittur, Elena Arthur, Maikhanh Nguyen, Chiu-Yueh Hung, David C Sane, Jiahua Xie

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Article in International journal of biological macromolecules, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.0field-weighted citation impact, top 23% 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

5 citing papers in PubMed, 9 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

6 authors at 2 institutions in 1 country.

Farooqahmed S KitturDepartment of Pharmaceutical Sciences, Biomanufacturing Research Institute & Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA.
Elena ArthurDepartment of Pharmaceutical Sciences, Biomanufacturing Research Institute & Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA.
Maikhanh NguyenDepartment of Pharmaceutical Sciences, Biomanufacturing Research Institute & Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA.
Chiu-Yueh HungDepartment of Pharmaceutical Sciences, Biomanufacturing Research Institute & Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA.
David C SaneCarilion Clinic and Virginia Tech Carilion School of Medicine, Roanoke, VA 24014, USA.
Jiahua XieDepartment of Pharmaceutical Sciences, Biomanufacturing Research Institute & Technology Enterprise, North Carolina Central University, Durham, NC 27707, USA. Electronic address: jxie@nccu.edu.
North Carolina Central University · USCarilion Clinic · US

Funding

Plant-produced Asialo-erythropoietin and its Antiapoptotic FunctionsSC3GM088084 · NIGMS · NORTH CAROLINA CENTRAL UNIVERSITY · PI XIE, JIAHUA · 2009 to 2012
$417k
NIGMS NIH HHS SC3 GM088084NIGMS NIH HHS SC3GM088084
6 · The paper itself

Abstract

Asialoerythropoietin (asialo-EPO) is a desialylated form of human glycoprotein hormone erythropoietin (EPO), which has been reported to be neuro-, cardio-, and renoprotective in animal models of organ injuries. Since the current method of production of asialo-EPO from mammalian cell-made recombinant human EPO (rhuEPO(M)) by enzymatic desialylation is not commercially viable, we and others used plant-based expression systems to produce recombinant human asialo-EPO (asialo-rhuEPO(P)). Despite achieving high expression levels in plants, its purification from plant extracts has remained a greater challenge, which has prevented studying its tissue-protective effects and translating it into clinical practice. In this study, a procedure was developed to purify asialo-rhuEPO(P) from transgenic tobacco leaf tissues in two steps: ion-exchange chromatography based on its high pI (8.75) to separate it from acidic plant proteins, and immunoaffinity chromatography to obtain pure asialo-rhuEPO(P). Using this process, up to 31% of the asialo-rhuEPO(P) could be recovered to near homogeneity from plant extracts. This work demonstrates that asialo-rhuEPO(P) expressed in tobacco plants could be purified in high yield and purity using minimal steps, which might be suitable for scale-up. Furthermore, the ion-exchange chromatography step together with the use of protein-specific antibody column could be used to purify a wide variety of basic recombinant proteins from transgenic leaf tissues.

Indexed as

AsialoglycoproteinsBiochemistryBlotting, WesternChromatography, AffinityChromatography, Ion ExchangeElectrophoresis, Polyacrylamide GelErythropoietinHumansHydrogen-Ion ConcentrationNicotianaPlant LeavesPlants, Genetically ModifiedRecombinant ProteinsasialoerythropoietinAsialoglycoproteinsErythropoietinRecombinant ProteinsBasic recombinant human proteinImmunoaffinity chromatographyIon-exchange chromatographyPlant-produced asialoerythropoietin

Identifiers

PMID25450830
PMCPMC4260996
OpenAlexW2004296555

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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.