Three analogs of Mast Cell Degranulating (MCD) peptide with C-terminal
and one analog with N- and C-terminal deletions were synthesized and
assayed for histamine releasing activity in mast cells. Des(20-22)-MCD
and des(21)-MCD markedly decreased this activity. In des(16-17,21)-MC
D this activity was completely abolished. By contrast, when the C-and
N-termini were truncated in des(1-2,20-22)-MCD, the full activity of M
CD peptide was restored. The possibility that these analogs trigger or
inhibit oxygen radicals from neutrophils was examined in a cell-free
system with a chemiluminescence assay. None of the above analogs exhib
ited inflammatory or anti-inflammatory activity. Changes in biological
activities were correlated with structural changes, as seen by circul
ar dichroism (CD) spectroscopy. (C) 1998 Elsevier Science Inc.