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Questions about a product, technology or experimental design? Give us a call 610-644-8845.

SUMO-Tag Protein Expression & Purification

Advanced protein expression solutions for superior yield, solubility, and native protein folding across prokaryotic and eukaryotic systems.

Protein expression and production of recombinant proteins routinely encounter problems, including formation of inclusion bodies, incorrect protein conformation, toxicity to the host cell, and low protein yield. These issues are most often addressed by using an alternative host or genetically fusing the protein of interest (POI) to a carrier protein (fusion tag).

Attachment of the C-terminus of SUMO (Small Ubiquitin-like Modifier) to the N-terminus of a protein of interest can dramatically improve protein solubility, achieve native protein folding, and increase total yield by improving expression and decreasing degradation.

LifeSensors protein expression system has pioneered SUMO fusion technology, which increases the quantity and quality of numerous recombinant proteins in both prokaryotic and eukaryotic expression hosts.

Our SUMO-tag expression system maximizes the yield of soluble, functional proteins in E. coli. SUMO functions as both a chaperone and initiator of protein folding, improving the solubility and yield of a POI. DeSUMOylases remove the SUMO tags, releasing your protein with the desired N-terminal amino acid. Both SUMO tags and deSUMOylases contain 6xHis tags allowing efficient subsequent removal, leaving pure protein.

SUMOpro System

Designed for expression and purification of proteins from E. coli

SUMOstar Tag

Engineered for eukaryotic hosts, resistant to endogenous proteases

Enhanced Expression

Preserves enhanced expression, increased solubility and native folding

Since all eukaryotic cells contain SUMO and SUMO proteases, the latter of which will cleave SUMO fusion proteins immediately following expression, LifeSensors has engineered SUMOstar, a SUMO tag for use in eukaryotic hosts, which is resistant to endogenous proteases, thus preserving enhanced expression, increased solubility and native folding. SUMOstar fusion proteins can be cleaved only with SUMOstar protease.

To overcome these challenges, we developed the SUMOstarâ„¢ tag, an engineered version of the SUMO fusion platform ideal for mammalian and insect expression due to its resistance to endogenous SUMO proteases found in all eukaryotic systems.

Bacteria

SUMOpro and SUMOstar tag systems for E. coli expression

SUMOstar Mammalian

Mammalian host expression systems

Advanced Therapeutic

Clinical-scale biotherapeutic production

Yeast

SUMOstar and SUMOpro3 for Pichia pastoris and Saccharomyces cerevisiae

Insect

SUMOstar for insect cell expression

The SUMOpro tag system is based off our SUMO protein expression platform to maximize the yield of soluble and functional proteins with a native N-terminus. Precise tag removal relies on LifeSensors’ highly specific SUMO proteases, which recognize the tertiary structure of the tag at the N-terminus of the partner protein and cleaves the junction at discrete residues outside the protein sequence.

Therefore, SUMO proteases are superior to other proteases commonly used in prokaryotic expression systems that may non-specifically cleave within the protein of interest or leave extra residues behind. By linking a His6 tag to both the SUMOpro fusion tag and SUMO protease, the system allows efficient and rapid purification of untagged proteins using immobilized metal affinity chromatography. SUMOpro fusion, thus, makes purifying your protein easy and affordable.

LifeSensors offers both yeast (SUMOpro) and human (SUMOpro3) tags with corresponding SUMO proteases 1 and 2, respectively for Bacterial Expression.

Service Highlights

Yeast, especially Pichia pastoris and Saccharomyces cerevisiae, are also commonly used for protein expression. LifeSensors offers both SUMOstar and SUMOpro3 systems for secretory expression in Pichia, while SUMOstar is available and recommended for Saccharomyces intracellular expression. SUMO Protease 2 is compatible with SUMOpro3 expression while SUMOstar Protease is designed to work with SUMOstar

Service Highlights

Insects like many eukaryotic organisms possesses endogenous SUMO proteases that will cleave a protein expressed with a traditional SUMO tag. The insect cell protein expression system, typically using the Baculovirus Expression Vector System (BEVS), involves cloning a target gene into a plasmid vector that generates a bacmid. This bacmid is used to create and amplify recombinant baculoviruses in insect cells such as SF9 expression a target protein. LifeSensors SUMOstar system is recommended for this application.

Service Highlights

While LifeSensors offers both yeast (SUMOpro) and human (SUMOpro3) tags with corresponding SUMO proteases 1 and 2, respectively, in mammalian expression endogenous SUMO proteases can cleave the protein, preventing expression and purification.

SUMOstar is designed to prevent the above issue by using an engineered SUMO tag to prevent cleavage and preserve the enhanced protein production properties of SUMO. Isolated SUMOstar fusions from eukaryotic cells can be cleaved efficiently via SUMOstar protease in vitro.

Service Highlights

Many new therapies are now being delivered as genes, mRNA, or AAV-mediated vehicles. Poor expression in prokaryotic and eukaryotic hosts is the primary cause of a lack of efficacy of these therapies. Clinical-scale production of functional biotherapeutics such as proteins used in CAR-T therapy and vaccine candidates routinely faces challenges of expression quantity, misfolding, incorrect localization, degradation in the host cell, and HIGH costs. However, clinical-scale production remains critical for successful therapeutic outcomes.
To overcome these challenges, we developed the SUMOstarâ„¢ tag, a modified version of the SUMO fusion platform ideal for mammalian expression due to its resistance to endogenous SUMO proteases found in all eukaryotic systems.
The SUMOstarâ„¢ tag remains tethered to the protein throughout the purification process. Precise C-terminal removal of the tag simply requires end user-induced cleavage by engineered SUMOstarâ„¢ proteases. The native N-terminal residues of the protein are completely preserved following cleavage, which is particularly important for researchers seeking biologically active cytokine-based therapeutic strategies.

Service Highlights

Application of SUMO System across the Biological Spectrum

SUMOpro technology is ideal for enhanced expression, increased solubility, and native folding in E. coli. The SUMOstar system presents similar advantages for native protein expression in mammalian cells.

Chemical synthesis of polypeptides is prone to errors. Not all chemically synthesized peptides fold correctly, and yield of polypeptides decreases along with the length of the polypeptide.

E. coli provides an attractive platform to express animal vaccines at a low cost. The SUMO system provides the capability to increase yield and serves as a tool to rapidly purify the antigen.

Although mammalian cells have proven to be workhorses for antibody production, engineered single chain antibodies (Nanobodies) are especially difficult to manufacture in mammalian cells. SUMOpro is an inexpensive method for Nanobody production.

Despite the strong promoters, many genes are not expressed well in recombinant adeno associated viruses (rAAV). LifeSensors has established a human SUMOstar based system that allows under expressed or non-expressed genes to be delivered as SUMOstar fusion between rAAV ITR containing plasmids.

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Our expert team is ready to help you optimize your protein expression and purification workflow

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