• Frozen / Standard (GLCD3-1) $ 895

G-link CD3 is a precision-engineered adapter protein that retargets lentiviral vectors (LV) to CD3, activating T cells and enhancing transduction in a single-step.

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How it Works:

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The G-Link CD3 adapter protein binds to wild-type VSV-G on the surface of LV particles and retargets them to CD3. In addition to G-binding and CD3-retargeting domains, the G-Link CD3 adapter protein includes a trimerizing linker, enabling high-avidity attachment to G. The adapter protein is designed to release in the endosome, allowing normal cell membrane fusion and cell transduction.

 

Precision Targeting:

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G-Link CD3 enables selective transduction of CD3-positive T cells. The G-Link CD3-targeting domain binds specifically to CD3 to mediate T-cell binding, while the G-binding domain not only anchors G-Link CD3 to G but also prevents G from binding to its natural receptors and the trimerizing linker enhancers overall adapter stability. Together, these components mask entry through native receptors while retargeting delivery to CD3. 

 

GFP-encoding LV pseudotyped with VSV-G was used directly or following retargeting with G-Link CD3 to transduce Jurkat (CD3+) and Jurkat-TCR-KO (CD3-) cells. GFP signal in the cells was imaged (left) and quantitated (right) 3 days post transduction. 

 

 

 

Enhanced Transduction of Resting T Cells: 

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G-Link CD3 boosts transduction of resting T cells simplifying workflows. LVs retargeted using G-Link CD3 effectively transduce and active T-cells in one-step, so PBMCs can be transduced without the need for pre-activation using beads or cytokine cocktails.  

Resting human PBMCs were transduced at 1000 LVP/cell with GFP-encoding (top) or BCMA-CAR-encoding (bottom) LVs pseudotyped with VSV-G. LVs were used directly (left) or retargeted using G-link (right). 

PBMCs were incubated with VSV-G-pseudotyped LV (left), VSV-G-pseudotyped lentivirus retargeted with G-Link CD3 (middle), or G-Link CD3 only (right). The T-cell activation marker CD25 was measured XX days after transduction. 

 

 

 

Targeted In Vivo Delivery: 

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G-Link CD3-retargeted LVs work in vivo to target and transduce T cells.  

 

 

 

NSG DKO mice bearing BCMA+ OPM2-luciferase tumors were humanized PBMCs. One week later (Day 0), mice were injected via tail vein with saline control, G-Link CD3 only, or BCMA-CAR encoding LV retargeted with G-Link CD3. Tumor burden was monitored over time by bioluminescence imaging.  

 

Produc

The G-Link CD3 Workflow: 

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