Sleeping Beauty Chimeric Antigen Receptor (CAR) Expression Vector


Utilizing chimeric antigen receptor (CAR) vectors to produce engineered T cells (also known as CAR T cells) that can recognize tumor-associated antigens has emerged as a promising approach in the treatment of cancer. In CAR T-cell therapy, T cells derived from either patients (autologous) or healthy donors (allogeneic) are modified to express CAR, a chimeric construct which combines antigen binding with T cell activation for targeting tumor cells.

Structurally, a CAR consists of four main components: (1) an extracellular antigen recognition domain made up of an antibody-derived single chain variable fragment (scFv) of known specificity. The scFv facilitates antigen binding and is composed of the variable light chain and heavy chain regions of an antigen-specific monoclonal antibody connected by a flexible linker; (2) an extracellular hinge or spacer which connects the scFv with the transmembrane domain and provides flexibility and stability to the CAR structure; (3) a transmembrane domain which anchors the CAR to the plasma membrane and bridges the extracellular hinge as well as antigen binding domain with the intracellular signaling domain. It plays a critical role in enhancing receptor expression and stability, and (4)an intracellular signaling domain that is typically derived from the CD3 zeta chain of the T cell receptor (TCR) and contains immunoreceptor tyrosine-based activation motifs (ITAMs). The ITAMs become phosphorylated and activate downstream signaling upon antigen binding, leading to the subsequent activation of T cells. In addition, the intracellular region may contain one or more costimulatory domains (derived from CD28, CD137, etc.) in tandem with the CD3 zeta signaling domain for improving T cell proliferation and persistence.

The structure of CAR has evolved over the past few years based on modifications to the composition of the intracellular domains. The first-generation CARs consisted of only a single intracellular CD3 zeta-derived signaling domain. While these CARs could activate T cells, they exhibited poor anti-tumor activity in vivo due to the low cytotoxicity and proliferation of T cells expressing such CARs. This led to the advent of second-generation CARs which included an intracellular costimulatory domain in addition to the CD3 zeta signaling domain leading to a significant improvement in the in vivo proliferation, expansion, and persistence of T cells expressing second-generation CARs. To further optimize the anti-tumor efficacy of CAR-T cells, third-generation CARs were developed which included two intracellular, cis-acting costimulatory domains in addition to CD3 zeta. Thereafter, fourth-generation CARs were derived from second-generation CARs by modifying their intracellular domain for inducible or constitutive expression of cytokines. The fifth and the latest generation of CARs are also derived from second-generation CARs by the incorporation of intracellular domains of cytokine receptors.

Our sleeping beauty CAR expression vector is a highly efficient tool for achieving non-viral, transposon-based delivery of second-generation CAR expression cassettes into T cells. This vector system is derived from the Tc1/mariner superfamily of transposons which were originally isolated from fish genomes and have been transpositionally inactive due to the accumulation of mutations. The sleeping beauty transposon was reconstructed by eliminating such inactivating mutations from sequences of Tc1/mariner transposons found in salmonids.

The sleeping beauty system comprises two components: the transposon plasmid and the transposase (helper). The transposon plasmid contains two inverted/direct repeats IR/DR(R) bracketing the region to be transposed. The transposase can be delivered into target cells through two methods. A helper plasmid encoding transposase can be transiently transfected into cells. Alternatively, target cells can be injected with in vitro transcribed transposase mRNA. When transposon plasmids and the helper are co-introduced into target cells, the transposase produced from the helper would recognize the two IR/DR(R)s on the transposon and insert the flanked region including the two IR/DR(R)s into TA dinucleotide sites of the host genome. At each insertion site, duplicated TA target sites are created, flanking the transposon in the genome. Through both methods of delivering transposase, it is expressed for only a short time. Upon the loss of the helper plasmid or degradation of transposase mRNA, the integration of the transposon into the host genome becomes permanent.

Sleeping Beauty is a class II transposon, meaning that it moves in a cut-and-paste manner, hopping from place to place without leaving copies behind (In contrast, class I transposons move in a copy-and-paste manner). If the sleeping beauty transposase is reintroduced into the cells, the transposon could be excised from the genome of some cells. The excision results in the formation of a “transposon footprint”, consisting of three nucleotides flanked by duplicated TA target sites.

For further information about this vector system, please refer to the papers below.

References Topic
J Clin Invest. 130:6021 (2021) Using sleeping beauty engineered CAR T cells to achieve antileukemic activity
Br J Cancer. 120:26 (2019) Review on next-generation CAR T cells
Mol Ther Oncolytics. 3:16014 (2016) Review on CAR models
J Immunother. 32:689 (2009) Construction and pre-clinical evaluation of an anti-CD19 CAR
Mol Ther. 17:1453 (2009) In vivo characterization of chimeric receptors containing CD137 signal transduction domains


Our sleeping beauty CAR expression vector is suitable for the expression of second-generation CARs. The sleeping beauty transposon plasmid along with the helper plasmid are optimized for high copy number replication in E. coli, efficient transfection into a wide range of target cells, and high-level expression of the transgene carried on the vector.


Permanent integration of vector DNA: The sleeping beauty CAR expression vector helps achieve long-term expression of CAR expression cassettes in T cells by allowing permanent integration of the transposon carrying the CAR cassette into the host cell genome.

Technical simplicity: Sleeping beauty-based CAR vectors can be delivered into T cells by electroporation which is technically simpler compared to using virus-based CAR constructs. Viral vectors require the packaging of live virus before they can be transduced into T cells, making the process technically challenging and time-consuming.

Low cost: Manufacturing of clinical-grade sleeping beauty vectors is far less expensive than viral vectors which makes clinical development of piggyBac-based CAR T cells much more cost-effective. This offers a significant advantage in the development of CAR T therapies since the clinical efficacy of CAR T cells cannot be accurately predicted by preclinical studies in mice models and should be determined by clinical studies.


Delivery method: Sleeping beauty-based CAR expressions vectors are typically delivered into T cells by electroporation which typically results in a low to medium frequency of cells with successful integration of the CAR expression cassette. Additionally, electroporation can be toxic to T cells which in turn could lead to reduced yield of functional CAR T cells. Therefore, it may be necessary to culture the T cells ex vivo for extended periods to attain the quantities needed for infusion, which over time could alter cell phenotype leading to reduced long-term memory function.

Limited transposon carrying capacity: For transposons between 1.9 and 7.2 Kb, transposition frequency decreases with increase in transposon length.

Key components

IR/DR(L): Inverted/direct repeats of sleeping beauty transposon (Left). Recognized by sleeping beauty transposase; DNA flanked by IR/DR(L) and IR/DR(R) can be transposed by sleeping beauty transposase into TA dinucleotide sites.

Promoter: The promoter driving your CAR expression cassette is placed here.

Kozak: Kozak consensus sequence. It is placed in front of the start codon of the ORF of interest because it is believed to facilitate translation initiation in eukaryotes.

CD8-leader: Leader signal peptide of T-cell surface glycoprotein CD8 alpha chain. Directs transport and localization of the protein to the T-cell surface.

scFv: Single chain variable fragment derived from a monoclonal antibody of known specificity. Recognizes cells in an antigen-specific manner.

Hinge: Extracellular hinge region of the CAR. Connects scFv with the transmembrane region providing stability and flexibilty for efficient CAR expression and function; enhances efficiency of tumor recognition; improves expansion of CAR-T cells.

Transmembrane domain: Transmembrane domain of the CAR. Anchors the CAR to the plasma membrane and bridges the extracellular hinge as well as antigen recognition domains with the intracellular signaling region; enhances receptor expression and stability.

Costimulatory domain: Intracellular costimulatory domain of the CAR. Improves overall survival, proliferation, and persistence of activated CAR-T cells.

CD3zeta: Intracellular domain of the T cell receptor-CD3ζ chain. Acts as a stimulatory molecule for activating T cell-mediated immune response.

BGH pA: Bovine growth hormone polyadenylation signal. It facilitates transcriptional termination of the upstream CAR expression cassette.

IR/DR(R): Inverted/direct repeats of sleeping beauty transposon (Right). Recognized by sleeping beauty transposase; DNA flanked by IR/DR(L) and IR/DR(R) can be transposed by sleeping beauty transposase into TA dinucleotide sites.

TATA: TA dinucleotide base-pairs. Increases sleeping beauty transposition efficiency.

Ampicillin: Ampicillin resistance gene. It allows the plasmid to be maintained by ampicillin selection in E. coli.

pUC ori: pUC origin of replication. Plasmids carrying this origin exist in high copy numbers in E. coli.

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