HCMV UL40 15-23 (HLA-E) VMAPRTLIL
€105.00*
Description
HCMV UL40 15-23 with the amino acid sequence VMAPRTLIL is a linear peptidic epitope (epitope ID 69921) that is an important negative regulator of natural killer cell activity. The HCMV UL40 15-23 peptide is often used as positive control.
HCMV UL40 15-23 is part of the immune evasion strategie of the Human Cytomegalovirus (HCMV). The virus downregulates HLA class Ia molecule expression in order to evade T cell recognition. However, a lack of surface HLA class Ia molecules triggers cytotoxicity of Natural Killer (NK) cells. To counteract this effect, the Cytomegalovirus promotes upregulation of HLA-E and provides the peptide HCMV UL40 15-23 (VMAPRTLIL), which mimics the leader sequence of HLA-Cw03 (VMAPRTLIL). When loaded onto HLA-E, this peptide conferres resistance to NK cell lysis via the CD94/NKG2A receptor.
HLA-E is presenting peptides derived from self-proteomic content and peptides of pathogenic origin. VMAPRTLIL is part of the following proteins of human origin:
- Major histocompatibility complex, class I, C (UniProt:A0A140T9M0, A0A140T9U0, A0A0G2JH50, A0A140T912 and A0A140T9Z4)
- HLA class I histocompatibility antigen C alpha chain (UniProt:Q53YP1, Q5RIP0)
- HLA class I antigen (UniProt:Q5QT33)
- Isoform 2 of HLA class I histocompatibility antigen, C alpha chain (UniProt:P10321-2)
TechData
| Sequence: | VMAPRTLIL |
| Gene: | UL111A |
| Delivery: | 1-3 days |
| C-Terminus: | OH |
| N-Terminus: | H |
| Amount: | 1 mg |
| Counterion: | TFA |
| Protein: | Viral interleukin-10 homolog |
| IEDB Id: | https://www.iedb.org/epitope/69921 |
| Species: | Human cytomegalovirus (Human herpesvirus 5) |
| Allele: | HLA-E* |
| Application: | Flow Cytometry |
| Indication: | Infectious disease, Cancer, Neuroscience, Diabetes |
| Purity: | 95% HPLC-MS |
Documents
References
Martín Almazán, Nerea et al. “Non-classical HLA-E restricted CMV 15-mer peptides are recognized by adaptive NK cells and induce memory responses.” Frontiers in immunology vol. 14 1230718. 21 Sep. 2023, doi:10.3389/fimmu.2023.1230718
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