Structure-activity relationship studies on the endogenous neuroactive tetrapeptide achatin-I on giant neurons of Achatina fulica Ferussac.

The structure-activity relationships of achatin-I, a neuroactive peptide containing a D-phenylalanine residue, for producing excitatory effects on three different types of Achatina neurons, PON, TAN and d-RCDN, were studied under the voltage clamp method. Of the peptides examined, only Gly-Gly-D-Phe-L-Ala-L-Asp (IV). D-Phe-L-Ala-L-Asp (V) and Gly-D-Phe-L-Ala-L-Asn (XVI) produced an inward current with increased membrane conductance similar to achatin-1 (I). The structure-activity relationship was essentially the same for the three Achatina neuron types. The equiactive molar ratios (EMRs) of the active peptides vs. achatin-I (I) were calculated from their dose-response curves: 8 - 60 for Gly-Gly-DPhe-L-Ala-L-Asp (IV), 200 - greater than 250 for D-Phe-L-Ala-L-Asp (V) and greater than 200 for Gly-D-Phe-L-Ala-L-Asn (XVI). These values indicate that the achatin-I receptor in the Achatina neurons is highly structure-specific.