Table 1.
Antigen | Peptide | Epitope name | Length (aa) | Biotinylated gp41 peptide |
---|---|---|---|---|
gp41 | S1 | N-terminal | 13 | Biotin-MQARQLLSGIVQQ |
S2 | Bacterial mimotope | 13 | Biotin-QQNNLLRAIEAQQ | |
S3 | HEPS | 18 | Biotin-GIKQLQARILAVERYLKD | |
S4 | Caveolin | 18 | SLEQIWNHTTWMEWDREI-K-Biotin | |
S5 | Transcytosis | 16 | EINNYTSLIHSLIEES-K-Biotin | |
gp41/P1 | S6 | 5F3 | 15 | SQTQQEKNEQELLEL-K-Biotin |
P1 | S7 | 2F5 | 17 | Biotin-NEQELLELDKWASLWNW |
P1 | S8 | 4E10/10E8 | 17 | Biotin-LWNWFNITNWLWYIKLS |
These peptides are captured in streptavidin coated ELISA plates and used for evaluating the gp41 epitope reactivity profile of vaccine-induced serum antibodies in rat. Peptides have 13–18 amino acids (a.a.) in length and were derived from various gp41 regions of the HIV-1 HXB2 clade B strain, starting from the amino-terminus to the carboxyl-terminal end. Peptides S1 and S2 were designed for monitoring the level of vaccine-induced serum reactivity toward the gp41 N-terminal region and the bacterial mimotope present on the gp41. For peptides S3–S8, the sequences are based on reported gp41 epitopes toward which antibodies may harbor antiviral activities (caveolin, transcytosis), a region recognized by neutralizing antibodies present in HEPS or by the 2F5 and 4E10/10E8 neutralizing monoclonal antibodies (mAb) harboring cross-strain and cross-clade activities, and the non-neutralizing epitope recognized by the 5F3 monoclonal antibody.