H-Leu-Ser-Pro-Phe-Pro-Phe-Asp-Leu-OH
| Name | H-Leu-Ser-Pro-Phe-Pro-Phe-Asp-Leu-OH |
| Category | Cancer Research Peptides |
| One Letter Code | LSPFPFDL |
| Three Letter Code | {Leu}{Ser}{Pro}{Phe}{Pro}{Phe}{Asp}{Leu} |
| Molecular Weight | 935.090 |
| Application | Cancer Research |
| Engels, Boris, et al. "Long-term persistence of CD4+ but rapid disappearance of CD8+ T cells expressing an MHC class I-restricted TCR of nanomolar affinity." Molecular Therapy 20.3 (2012): 652-660. |
| Kageyama, Shigeki, et al. "Potent cytolytic response by a CD8+ CTL clone to multiple peptides from the same protein in association with an allogeneic class I MHC molecule." The Journal of Immunology 166.5 (2001): 3028-3034. |
| Lebowitz, Michael S., et al. "Soluble, high-affinity dimers of T-cell receptors and class II major histocompatibility complexes: biochemical probes for analysis and modulation of immune responses." Cellular immunology 192.2 (1999): 175-184. |
| O'Herrin, Sean M., et al. "Analysis of the expression of peptide–major histocompatibility complexes using high affinity soluble divalent T cell receptors." The Journal of experimental medicine 186.8 (1997): 1333-1345. |
| Dutz, Jan P., et al. "A cytotoxic T lymphocyte clone can recognize the same naturally occurring self peptide in association with a self and a nonself class I MHC protein." Molecular immunology 31.13 (1994): 967-975. |