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Lcmv gp61 80

Manufactured by AnaSpec

The LCMV gp61-80 is a peptide that is derived from the lymphocytic choriomeningitis virus (LCMV) glycoprotein. It represents a specific region (amino acids 61-80) of the LCMV glycoprotein. This peptide is commonly used in research applications involving LCMV.

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2 protocols using lcmv gp61 80

1

Activation of Murine T Cells with Rexinoids

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Spleens were harvested from B6.Cg-Tcratm1MomTg(TcrLCMV)327Sdz/TacMmjax (P14), B6.Cg-PtprcaPepcbTg(TcrLCMV)1Aox/PpmJ (SMARTA), or C57BL/6-Tg(TcraTcrb)1100Mjb/J (OT-1) transgenic mice (Jackson Labs) and mechanically dissociated into a single cell suspension using a 70μm nylon mesh strainer (Fisherbrand). All mouse experiments were conducted under institutional care and use committee approval. T cells were stimulated with 1μg/mL of appropriate viral peptide (LCMV gp33-41, LCMV gp61-80, or OVA257-264, respectively) (GenScript; Anaspec). Cells were cultured in a 96-well plate for 8 days using RPMI complete medium (10% FBS, 1% PSG 100X) supplemented with 2.5x10-5 μg/μL IL-2 (Gibco) and 100nM of indicated rexinoid treatment or ATRA in a final volume of 200μL. 8 day treatment timeframe was determined using a time course assay (Supplementary Figure 1). Fresh culture medium with IL-2 and rexinoid or ATRA was replaced every 48 hours. Vitamin A deficient media was made using charcoal-stripped FBS (ThermoFisher).
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2

Antigen-Specific T Cell Activation by DCs

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For DC transfer experiments, splenic DCs were isolated as described above from mice subcutaneously injected with 1 × 106 B16 melanoma cells that constitutively secrete FMS-like tyrosine kinase 3 ligand (Flt3L)58 (link) 10 days prior to harvest. Cells were resuspended at 107 cells/ml and incubated with 10 μM OVA323–339, LCMV-GP61–80, OVA257–264, or LCMV276–286 peptides (Anaspec) in RPMI + 10% FBS, for 30 min at 37 °C. For cell labelling, CFSE or CTV (ThermoFisher Scientific) was added to a final concentration of 2 μM during the last 5 or 20 minutes of incubation, respectively. Cells were washed three times in RPMI + 10% FBS and resuspended at 2 × 107 cells/ml in PBS supplemented with 0.4 μg ml−1 LPS (Sigma-Aldrich). DCs were injected (5 × 105 cells in 25 μl) subcutaneously into the hind footpads. For CD4+ T cell and CD8+ T cell transfer experiments, T cells isolated as described above were injected intravenously in 100 μl PBS per mouse.
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