Evidence map›Paper›PMID 32816073›Full record

ArticleBioprocess and biosystems engineering2021

A scalable insect cell-based production process of the human recombinant BMX for in-vitro covalent ligand high-throughput screening.

Bárbara B Sousa, Marcos F Q Sousa, Marta C Marques, João D Seixas, José A Brito, Pedro M Matias, Gonçalo J L Bernardes, António Roldão

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in Bioprocess and biosystems engineering, 2021. 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
0.1field-weighted citation impact, top 55% 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, 2 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 2 countries.

Bárbara B Sousa *Instituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
Marcos F Q Sousa *Instituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. Da República, EAN, 2780-157, Oeiras, Portugal.ORCID http://orcid.org/0000-0003-3766-3900
Marta C MarquesInstituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
João D SeixasInstituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
José A BritoInstituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. Da República, EAN, 2780-157, Oeiras, Portugal.
Pedro M MatiasInstituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. Da República, EAN, 2780-157, Oeiras, Portugal.
Gonçalo J L BernardesInstituto de Medicina Molecular João Lobo Antunes, Faculdade de Medicina, Universidade de Lisboa, Avenida Professor Egas Moniz, 1649-028, Lisboa, Portugal.
António RoldãoInstituto de Tecnologia Química e Biológica António Xavier, Universidade Nova de Lisboa, Av. Da República, EAN, 2780-157, Oeiras, Portugal. aroldao@ibet.pt.
University of Lisbon · PTInstituto de Biologia Experimental e Tecnológica · PTUniversidade Nova de Lisboa · PT

Funding

FCT/ Ministério da Educação e Ciência (IF/01704/2014/CP1229/CT0001)FCT/ Ministério da Educação e Ciência Investigador FCT programme 2014FCT/ Ministério da Educação e Ciência (project IF/01704/2014)Fundação para Ciência e Tecnologia, FCT/MCTES, FEDER, and Programa Operacional Competitividade e Internacionalização (POCI) iNOVA4 Health Research UnitFundação para Ciência e Tecnologia, FCT/MCTES, FEDER, and Programa Operacional Competitividade e Internacionalização (POCI) (LISBOA-01-0145-FEDER-007344)Royal Society Marie Sklodowska-Curie IF
6 · The paper itself

Abstract

Bone Marrow Tyrosine kinase in the chromosome X (BMX) is a TEC family kinase associated with numerous pathological pathways in cancer cells. Covalent inhibition of BMX activity holds promise as a therapeutic approach against cancer. To screen for potent and selective covalent BMX inhibitors, large quantities of highly pure BMX are normally required which is challenging with the currently available production and purification processes. Here, we developed a scalable production process for the human recombinant BMX (hrBMX) using the insect cell-baculovirus expression vector system. Comparable expression levels were obtained in small-scale shake flasks (13 mL) and in stirred-tank bioreactors (STB, 5 L). A two-step chromatographic-based process was implemented, reducing purification times by 75% when compared to traditional processes, while maintaining hrBMX stability. The final production yield was 24 mg of purified hrBMX per litter of cell culture, with a purity of > 99%. Product quality was assessed and confirmed through a series of biochemical and biophysical assays, including circular dichroism and dynamic light scattering. Overall, the platform herein developed was capable of generating 100 mg purified hrBMX from 5 L STB in just 34 days, thus having the potential to assist in-vitro covalent ligand high-throughput screening for BMX activity inhibition.

Indexed as

BioreactorsCell Culture TechniquesAnimalsHumansProtein-Tyrosine KinasesRecombinant ProteinsSf9 CellsSpodopteraBMX protein, humanProtein-Tyrosine KinasesRecombinant ProteinsBioprocess developmentCancer therapyhrBMX crystallizationhrBMX productionIC-BEVS

Identifiers

PMID32816073
OpenAlexW3050009087

What OpenQuestion holds

Textmetadata
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.