Table 1.

NH2-terminal sequence analysis and mass spectrometry of CD26/DPP IV–treated chemokines

ChemokineNH2-terminal sequence*Reduction inMr
UntreatedCD26/DPP IV–treatedTheoreticalObserved
Met-IP-10 MVPLSRTVRCTC MVPLSRTVRCTC 
IP-10 VPLSRTVRCTC LSRTVRCTC 196.25 196.9 ± 0.4 
Mig TPVVRKGRCSC VVRKGRCSC 198.22 197.7 ± 0.4 
I-TAC FPMFKRGRCLC MFKRGRCLC 244.29 243.9 ± 0.3 
ChemokineNH2-terminal sequence*Reduction inMr
UntreatedCD26/DPP IV–treatedTheoreticalObserved
Met-IP-10 MVPLSRTVRCTC MVPLSRTVRCTC 
IP-10 VPLSRTVRCTC LSRTVRCTC 196.25 196.9 ± 0.4 
Mig TPVVRKGRCSC VVRKGRCSC 198.22 197.7 ± 0.4 
I-TAC FPMFKRGRCLC MFKRGRCLC 244.29 243.9 ± 0.3 

Single-letter amino acid abbreviations used.

*

The NH2-terminal sequence of untreated and CD26/DPP IV–treated (18-hour incubation) chemokines was determined by automated Edman degradation.

The average (± SD) difference between theMr of intact and truncated CXCR3 ligands was calculated from mass measurements on 4 different incubations (between 2 and 30 minutes) with CD26/DPP IV (25 U/L).

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