TABLE 1.
a Purity was determined by analytical RP-HPLC (Vydac C18, 5 μm, 4 × 250 mm) and a binary solvent system (A: H2O/CH3CN/TFA (99/1/0.1); B: CH3CN/H2O/TFA (90/10/0.07)) with a linear gradient of solvent B over 20 min. Flow rate was at 1 ml/min and elution was monitored at by absorbance at 230 nm.
b Expected molecular weights were calculated using Peptide mass calculator version 3.2.
c Observed molecular weights were determined by MALDI-TOF MS in positive reflectron mode using α-cyano-4-hydroxycinnamic acid as the matrix.
d KGG spacer coupled to the N terminus of the peptide before pegylation.
e GG spacer coupled to the N terminus of the peptide before pegylation.