Home -> Genomics -> Gene Integration -> PinPoint Targeted Integration System

PinPoint Targeted Integration System

• Create stable isogenic cell lines at defined loci
• High efficiency insertion with no size limit
• Avoid gene integration site variation
• High-throughput cell line engineering

The PinPoint Targeted Integration system allows users to easily and efficiently create isogenic stable cell lines in mammalian and other cell types. Custom gene expression cassettes can be engineered into target genomes using the unique PinPoint integrase with site-specific control. This technology enables the generation of platform cell lines which can be used to routinely knock-in different transgenes and reporters at the same genetic locus in cells with the same genetic background. This level of targeting control allows for the study of phenotypic effects free from context and positional variations, which results in more accurate genotype to phenotype correlations. The PinPoint integrase can be used in combination with TALEN and Cas9 systems to provide high-throughput cell line engineering anywhere in the genome.

How the PinPoint system works
The PinPoint system is a two-step approach for engineering of target cells with an optional third step for selection cassette removal by Cre resolvase.

Image

The first step involves insertion of a plasmid bearing the PinPoint placement site via transfection into the target cell genome. This can be done using two distinct approaches: i) the PinPoint-FC system that involves the well-characterized phiC31 integrase system or ii) the PinPoint-HR system that uses either TALE-Nuclease or Cas9 genome engineering tools to induce a double-stranded DNA break in the genome and insertion of the PinPoint placement site by homology-directed recombination (HDR) in a site-specific manner.

The second part of the PinPoint system relies on the introduction of a donor vector containing your desired gene cassette insert, which is integrated into the placed PinPoint site using a hyperspecific and efficient PinPoint integrase. The PinPoint integrase catalyzes the attB x attP reaction between the placed site (attP) and the attB site in the donor vector to insert the donor vector at the placed site each and every targeting event.

The third optional step invloves the removal of the entire backbone (excluding the insert and its promoter) using the well-characterized Cre/LoxP reaction leaving only the promoter/insert combination (and a single LoxP site) in the genome

Target site placement with the PinPoint-FC system
Platform cell lines containing the PinPoint attP site can be made through two different approaches. The PinPoint-FC system utilizes the phiC31 integrase (Cat# FC200A-1-SBI) along with the PinPoint-FC attP Placement Vector (Cat# PIN300A-1-SBI). This will integrate the cassette at pseudo attP sites within the targeted genome with typically single copy insertions.

Image

Target site placement with the PinPoint-HR system
Alternatively, the PinPoint-HR system uses a site-directed placement strategy. Customized placement can be achieved using the HR vector PIN400A-1-SBI. First, clone the homology arms for the desired integration site into the 5´ and 3´ MCS features. Then use this vector in combination with matched TALENs or Cas9 nuclease vectors. For more information on assembling TALENs and about building Cas9 vectors, see links below. SBI has created a safe-harbor PinPoint placement vector (Cat# PIN410A-1-SBI) to insert the attP site at the human AAVS1 genomic locus for routine integration of gene expression cassettes at this site.

Image



PinPoint site targeting
Once the PinPoint attP site has been successfully placed into the desired genomic site, this site can then be efficiently and routinely targeted for site-specific integration of expression cassettes at that locus. The expression cassette can be driven by EF1a (Cat# PIN500A-1-SBI), CAGs (Cat# PIN510A-1-SBI), or a custom-designed promoter of your choice (Cat# PIN520A-1-SBI). Once the gene or reporter of interest has been cloned into the PinPoint donor vector, a simple co-transfection of the placed attP site cell line with the PinPoint integrase vector (Cat# PIN200A-1-SBI) will result in a specific recombination reaction between the PinPoint attP site and the attB site in the donor vector construct.


PinPoint integrase and donor vectors
Image


Sample Data for PinPoint site placement and targeting

Pinpoint-FC attP placement
The PinPoint attP site was efficiently placed into HEK293 cells or HeLa cells. Approximately 8x10^5 cells were transfected with 40 ng PinPoint-FC placement vector (Cat# PIN300A-1-SBI) and 1,960 ng phiC31 integrase expression vector (Cat# PIN200A-1-SBI) at a 1:50 ratio, respectively. Positive cells were selected with 400 ug/ml G418 for 14 days. Six separate lines of HEK293 and HeLa cells were picked and expanded. After 11 days, the cells were fixed and stained with a solution of 50% methanol plus 1% methylene blue. The plates were washed twice with PBS and allowed to air dry. The number of visible colonies were imaged and colony number counts assessed.

Neomycin resistant HEK293 cells with placed PinPoint site

Image

These lines were then transfected with a control PinPoint Gene Donor vector (PIN600A-1-SBI) for precise integration. Unlike the R4 integrase used in a similar system, the PinPoint integrase does not recognize pseudo-sites and will only integrate at its placed recognition sequence. This feature results in the increased efficiency of correctly retargeted cell lines compared to the R4 integrase system. The entire therapeutic gene expression cassette is active and fully insulated with cHS4 DNA elements.


Neomycin resistant HEK293 cells with placed PinPoint site
Image

To verify that the PinPoint donor construct targeted to the correct site, junction PCR can be employed to amplify across the PinPoint integrase recombination site (attL) junction. Primers are designed within the placed puromycin marker cassette and within the PGK promoter are used in nested PCR reactions to verify the correct PinPoint integration structure. Three separate HEK293 colonies that were GFP positive were expanded for 3 days with subsequent genomic DNA isolation. Approximately 50 ng of genomic DNA was used in the nested PCR reactions and the products separated on 2% agarose gels and stained with ethidium bromide before imaging. The results clearly indiavcte the predicted, PinPoint integrase-mediated insertion of the donor vector PIN600a-1-SBI at the placed attP site with high precision.


Image

Related Links

phiC31 Integrase Vector System

 

 

Description Cat# Size Price    
PinPoint Integrase Expression Plasmid PIN200A-1-SBI 10 ug 782 € DETAILS   Add to Cart 
PinPoint-FC attP Placement Vector PIN300A-1-SBI 10 ug 806 € DETAILS   Add to Cart 
PinPoint-FC System for Platform Cell Line Generation and Retargeting (includes PIN300A-1, FC200PA-1, PIN200A-1, PIN510A-1 and PIN600A-1) PIN300A-KIT-SBI 1 kit 2709 € DETAILS   Add to Cart 
PinPoint-FC 293T Platform Cell Line for Targeted Gene Insertion with PinPoint site already placed PIN320A-1-GVO-SBI >2x10^5 cells 2997 € DETAILS   Add to Cart 
PinPoint-FC 293T Platform Kit for Targeted Gene Insertion (includes PIN320A-1, PIN200A-1, PIN510A-1 and PIN600A-1) PIN320A-KIT-GVO-SBI 1 kit 4727 € DETAILS   Add to Cart 
PinPoint-FC Murine iPSC Platform Cell Line for Targeted Gene Insertion with PinPoint site already placed PIN340iPS-1-GVO-SBI >2x10^5 cells 2997 € DETAILS   Add to Cart 
PinPoint-FC Murine iPSC Platform Kit for Targeted Gene Insertion (includes PIN340iPS-1, PIN200A-1, PIN510A-1 and PIN600A-1) PIN340iPS-KIT-GVO-SBI 1 kit 4727 € DETAILS   Add to Cart 
PinPoint-HR attP Placement Vector PIN400A-1-SBI 10 ug 1267 € DETAILS   Add to Cart 
PinPoint-HR System for Platform Cell Line Generation and Retargeting (includes PIN400A-1, PIN200A-1, PIN510A-1 and PIN600A-1) PIN400A-KIT-SBI 1 kit 2709 € DETAILS   Add to Cart 
PinPoint-HR attP Placement Vector PIN410A-1-SBI 10 ug 1267 € DETAILS   Add to Cart 
PinPoint-HR System for Platform Cell Line Generation and Retargeting of AAVS1 Safe Harbor Locus (includes PIN410A-1, GE601A-1, PIN200A-1, PIN510A-1 and PIN600A-1) PIN410A-KIT-SBI 1 kit 4158 € DETAILS   Add to Cart 
PinPoint-HR System for Platform Cell Line Generation and Retargeting of AAVS1 Safe Harbor Locus (includes PIN410A-1, CAS601A-1, PIN200A-1, PIN510A-1, and PIN600A-1) PIN412A-KIT-SBI 1 Kit 4158 € DETAILS   Add to Cart 
EF1alpha PinPoint Donor Vector (pPP-EF1a-MCS-pA-attB-Puro-pA) PIN500A-1-SBI 10 ug 1036 € DETAILS   Add to Cart 
CAG PinPoint Donor Vector (pPP-CAG-MCS-WPRE-pA-attB-Puro-pA) PIN510A-1-SBI 10 ug 1036 € DETAILS   Add to Cart 
Empty PinPoint Donor Vector (pPP-MCS-WPRE-pA-attB-Puro-pA) PIN520A-1-SBI 10 ug 1036 € DETAILS   Add to Cart 
PinPoint Donor Positive Control Vector: CAG->GFP+Luciferase (pPP-CAG-GFP-T2A-Luc-WPRE-pA-attB-Puro-pA) PIN600A-1-SBI 10 ug 1036 € DETAILS   Add to Cart 
PinPoint Donor Positive Control Vector: CM->Luciferase (pPP-CMV-Luc-pA-attB-Puro-pA) PIN610A-1-SBI 10 ug 1036 € DETAILS   Add to Cart 
Cre Recombinase Expression Plasmid (pCMV-CRE) CRE100A-1-SBI 10 ug 524 € DETAILS   Add to Cart 

BioCat Summer Special

% Special Offers

Benefit from our current promotions

SARS-CoV-2 / COVID-19

NEW! Tools for
SARS-CoV-2
Research

Electrophoresis

30% OFF BioCat Universal Agarose

DNA and RNA Purification

Bioline

Use ISOLATE II Nucleic Acid Isolation Kits for the purification of high-quality DNA and RNA.

Email Newsletter

Subscribe to the BioCat Email Newsletter.

Clone Resources

BioCat Clone Resources

Browse two of the most renowned clone resources of full-length cDNA, ORF, and shRNA clones as well as siRNA and yeast knockout strains.

Genome Engineering

Genome Engineering

Use the CRISPR/Cas9 SmartNuclease System to edit the genome.

ExoQuick and ExoQuick-TC

ExoQuick Exosome Isolation

Benefit from the most cited exosome isolation reagent for efficient exosome isolation and exosomal RNA purification from biofluids or culture media.

Home
Imprint / Impressum | Privacy Policy / Datenschutzerklärung
Top of Page Up!