TABLE 3.
HIV-1 and FIV PR cleavage of FIV PR selected phage-derived peptidesa
| Peptide | Peptide sequencec | HIV-1 PR cleavageb | FIV PR cleavageb |
|---|---|---|---|
| R3 20 | KGSGVF↓AVTQLVPK | ++ | +++ |
| R2 13 | KGSGIY↓TVQSLVPK | ++ | +++ |
| R1 8 | KGSGLTM↓VTQLVPK | − | +++ |
| R3 21 | KGSGVY↓QL d SALVPK | + | ++, ++d |
| R2 20 | KGSGALTN↓AVLVPK | − | +++ |
| R3 14 | KGSGAMVN↓QALVPK | − | +++ |
| R3 25 | KGSGTW↓MVHSLVPK | − | +++ |
| R3 30 | KGSGGRIN↓VALVPK | + | +++ |
All peptide sequences listed above were derived from phage selected as described in Materials and Methods. A 500 μM concentration of each peptide was digested with 312 nM FIV PR or 160 nM HIV-1 PR for 2 h at pH 6.7 in 0.2 M NaCl.
−, peptide cleavage not detected by HPLC; +, peptide cleavage detected at <5%; ++, peptide cleavage detected at between 10 and 90%; +++, 100% cleavage of the peptide.
Cleavage site for both HIV-1 PR and FIV PR is denoted by an arrow as determined by mass spectrometry of the cleaved fragments.
FIV PR cleaved peptide R3 21 at two sites, the second marked by this footnote reference. None of the starting peptide remained after cleavage, and each product was identified at >20% of the original peptide concentration.