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De novo optimized cell-free system for expression of soluble and active human tumor necrosis factor-alpha
by
El-Baky, Nawal Abd
, El-Helow, Ehab R.
, Sabry, Amira
, Redwan, Elrashdy Mustafa
, Sabry, Soraya A.
, EL-Fakharany, Esmail M.
in
Amino acids
/ anticancer
/ antineoplastic activity
/ Antitumor activity
/ Biological activity
/ cell-free protein synthesis
/ Cell-free system
/ Clinical trials
/ Cloning
/ Cytokines
/ Cytotoxicity
/ Design
/ DNA polymerase
/ E coli
/ Escherichia coli
/ genes
/ human tumor necrosis factor-alpha
/ humans
/ in vitro protein synthesis
/ Inflammation
/ neoplasm cells
/ Optimization
/ Protein biosynthesis
/ Protein expression
/ Protein structure
/ Protein synthesis
/ Proteins
/ recombinant proteins
/ response surface methodology
/ temperature
/ Tumor cell lines
/ tumor necrosis factor-alpha
/ Tumor necrosis factor-TNF
/ Tumor necrosis factor-α
/ Web sites
2022
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De novo optimized cell-free system for expression of soluble and active human tumor necrosis factor-alpha
by
El-Baky, Nawal Abd
, El-Helow, Ehab R.
, Sabry, Amira
, Redwan, Elrashdy Mustafa
, Sabry, Soraya A.
, EL-Fakharany, Esmail M.
in
Amino acids
/ anticancer
/ antineoplastic activity
/ Antitumor activity
/ Biological activity
/ cell-free protein synthesis
/ Cell-free system
/ Clinical trials
/ Cloning
/ Cytokines
/ Cytotoxicity
/ Design
/ DNA polymerase
/ E coli
/ Escherichia coli
/ genes
/ human tumor necrosis factor-alpha
/ humans
/ in vitro protein synthesis
/ Inflammation
/ neoplasm cells
/ Optimization
/ Protein biosynthesis
/ Protein expression
/ Protein structure
/ Protein synthesis
/ Proteins
/ recombinant proteins
/ response surface methodology
/ temperature
/ Tumor cell lines
/ tumor necrosis factor-alpha
/ Tumor necrosis factor-TNF
/ Tumor necrosis factor-α
/ Web sites
2022
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De novo optimized cell-free system for expression of soluble and active human tumor necrosis factor-alpha
by
El-Baky, Nawal Abd
, El-Helow, Ehab R.
, Sabry, Amira
, Redwan, Elrashdy Mustafa
, Sabry, Soraya A.
, EL-Fakharany, Esmail M.
in
Amino acids
/ anticancer
/ antineoplastic activity
/ Antitumor activity
/ Biological activity
/ cell-free protein synthesis
/ Cell-free system
/ Clinical trials
/ Cloning
/ Cytokines
/ Cytotoxicity
/ Design
/ DNA polymerase
/ E coli
/ Escherichia coli
/ genes
/ human tumor necrosis factor-alpha
/ humans
/ in vitro protein synthesis
/ Inflammation
/ neoplasm cells
/ Optimization
/ Protein biosynthesis
/ Protein expression
/ Protein structure
/ Protein synthesis
/ Proteins
/ recombinant proteins
/ response surface methodology
/ temperature
/ Tumor cell lines
/ tumor necrosis factor-alpha
/ Tumor necrosis factor-TNF
/ Tumor necrosis factor-α
/ Web sites
2022
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De novo optimized cell-free system for expression of soluble and active human tumor necrosis factor-alpha
Journal Article
De novo optimized cell-free system for expression of soluble and active human tumor necrosis factor-alpha
2022
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Overview
Cell-free (in vitro) expression is a robust alternative platform to the cell-based (in vivo) system for recombinant protein production. Tumor necrosis factor-alpha (TNF-α) is an effective pro-inflammatory cytokine with pleiotropic effects. The aim of the current study was de novo optimized expression of soluble and active human TNF-α by an in vitro method in an E. coli-based cell-free protein synthesis (CFPS) system and its biological activity evaluation. The codon-optimized synthetic human TNF-α gene was constructed by a two-step PCR, cloned into pET101/D-TOPO vector and then expressed by the E. coli CFPS system. Cell-free expression of the soluble protein was optimized using a response surface methodology (RSM). The anticancer activity of purified human TNF-α was assessed against three human cancer cell lines: Caco-2, HepG-2 and MCF-7. Data from RSM revealed that the lowest value (7.2 µg/mL) of cell-free production of recombinant human TNF-α (rhTNF-α) was obtained at a certain incubation time (6 h) and incubation temperature (20 °C), while the highest value (350 µg/mL) was recorded at 4 h and 35 °C. This rhTNF-α showed a significant anticancer potency. Our findings suggest a cell-free expression system as an alternative platform for producing soluble and functionally active recombinant TNF-α for further research and clinical trials.
Publisher
MDPI AG,MDPI
Subject
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