PEF Services
The PEF production pipeline provides a quick snapshot of the services we offer to help fast-track your research. From the Gene-to-Protein complete package to any stage in-between, we can customise to suit your project.Contact us to discuss how we can help support your research. Download the complete list as a pdf here.
Molecular Cloning
Molecular Cloning | |
Gene synthesis |
Generate the DNA sequence of a gene of interest. Codon optimisation (optional) for the host expression system. |
Expression construct |
Clone the gene of interest into chosen expression vector. DNA sequence verification of cloned construct. |
Mutagenesis |
Single or multiple nucleotide base change e.g. amino acid substitution, insert/delete restriction enzyme site, stop codon and small tag. DNA sequence verification of cloned construct. |
Plasmid production |
Production and purification of plasmid DNA from mini- to mega-prep scale. |
Small-scale Expression Screening
Small-scale Expression Screening | |
E. coli |
Expression screen in multiple conditions. Each construct tested in two different expression strains, two temperatures and two media. Analyse expression and Ni-NTA binding by SDS-PAGE. Resin-binding assay for polyhistidine-tagged constructs only. Determine optimal expression condition. |
Pichia pastoris |
Expression screen of 10 yeast clones per construct. Analyse expression and Ni-NTA binding by SDS-PAGE. Resin-binding assay for polyhistidine-tagged constructs only. Determine optimal expression condition. |
Insect cell/baculovirus |
Expression screen in multiple conditions. Each construct tested in two cell lines and at two temperatures. Analyse expression and Ni-NTA binding by SDS-PAGE and/or Western blot. Resin-binding assay for polyhistidine-tagged constructs only. Determine optimal expression condition. |
Mammalian cell |
Transient expression screen in two cell lines. Analyse expression and Ni-NTA binding by SDS-PAGE and/or Western blot. Resin-binding assay for polyhistidine-tagged constructs only. Determine optimal expression condition |
In vitro cell-free |
Expression screen using Leishmania tarentolae lysate. Analyse expression by SDS-PAGE. |
Large-scale Protein Expression
Large-scale Protein Expression | |
E. coli or Pichia pastorisexpression in shake flask |
Expression culture at ≥ 1 L in shake flasks. Cells and/or supernatant collected at optimal time of harvest. Analysis by SDS-PAGE. |
Insect cell/baculovirus expression in shake flask |
Scale-up of virus stock. Expression culture at ≥ 1 L in shake flasks. Cells and/or supernatant collected at optimal time of harvest. Analysis by SDS-PAGE and/or Western blot. |
Mammalian cell transient expression in shake flask |
Maxi-prep plasmid production. Expression culture at ≥ 1 L in shake flasks. Cells and/or supernatant collected at optimal time of harvest. Analysis by SDS-PAGE and/or Western blot. |
E. coli or Pichia pastorisfermentation in bioreactor |
Fermentation in a stirred tank bioreactor, from 2 L to 20 L. Analysis by SDS-PAGE. |
Insect or mammalian cell expression in bioreactor |
Expression in a WAVE bioreactor, from 1 L to 25 L. Analysis by SDS-PAGE and/or Western blot. |
Protein Purification
Protein Purification | |
Primary purification from cell pellet |
Sample extraction followed by affinity chromatography (e.g. IMAC, GST, MBP, Strep(ll), heparin). Analysis by SDS-PAGE. |
Primary purification from supernatant |
Tangential flow ultrafiltration for sample concentration and buffer exchange. Primary purification by affinity chromatography (e.g. IMAC, GST, MBP, Strep(ll), heparin, Protein A). Analysis by SDS-PAGE. |
Secondary or polishing purification |
Secondary or polishing purification to improve product purity by chromatography techniques such as affinity, ion exchange, hydrophobic interaction or gel filtration. Analysis by SDS PAGE. |
Fusion tag removal |
Scout optimal protease cleavage condition to remove fusion tag from protein. Proteases used are Enterokinase, Factor Xa, HRV-3C, SUMO, TEV or Thrombin. Chromatography to recover untagged protein. Analysis by SDS PAGE. |
Endotoxin removal |
Removal of endotoxin from purified protein. Analysis by SDS-PAGE and endotoxin determination by FDA-licensed LAL cartridges. |
Protein Characterisation and Analysis
Protein Characterisation and Analysis | |
Endotoxin measurement |
Endotoxin level determination by FDA-licensed LAL cartridges (for samples prior to animal studies) |
Mass spectrometry - intact protein analysis |
Accurately determine native protein molecular weight of purified sample |
Mass spectrometry - peptide mass fingerprint |
Identification of purified protein or excised band from polyacrylamide gel |
Analytical size exclusion chromatography |
Estimate native protein molecular weight, determine multimeric structure and degree of aggregation |
Dynamic light scattering |
Determine size distribution profile of proteins and protein complexes. Suitable for high throughput detection of protein aggregation, thermal stability and storage conditions |
Asymmetric flow-field flow-fractionation |
Accurately determine size distribution profile of virus-like particles and protein complexes |
Transmission electron microscopy |
Imaging and morphological characterisation of virus-like particles and protein complexes |