Antibody Detection of Marihuana

A reliable chemical means of assaying small quantities of marihuana or tetrahydrocannabinol (THC) isomers in body fluids and cell preparations has long been sought. A possible immunological approach was suggested by work with oestrogen haptens. It was established earlier that diazobenzoic acid under appropriate conditions enters the A ring by virtue of the phenolic function of C-3, yielding oestrogen azobenzoic acid derivatives^{1, 2}. These compounds are coupled readily through the benzoyl carboxyl to proteins and solid matrices containing accessible NH₂ groups, retaining the important antigenic specificities contributed by the reactive ?OH and = O groups as well as those associated with the ringed backbone^{1, 3}. Other biologically important molecules which lend themselves to similar manipulation are the principal psychotomimetics. In our search for useful haptens and active antibodies to be used in a reliable model assay system, we have chosen to report the investigation of THC. Similar results have been achieved with the phenanthrene alkaloids (S. J. G., unpublished) preserving all the determinant functional groups ^* unlike the reagent for morphine assay recently reported⁴.     

The Effect of Proteases on Gene Expression and Cell Differentiation in Dictyostelium discoideum

We have examined the effects of chymotrypsin or pronase on the differentiation of monolayers of Dictyostelium discoideum amoebae developing in the presence of 1–5 mM cyclic AMP. Using sporogenous mutants, which are capable of forming both spores and stalk cells under these conditions, we have observed that low concentrations of either protease selectively inhibit a late step of spore formation. Higher levels of the proteases act at an earlier time and by a distinct mechanism to reduce the accumulation of the prespore cell specific enzyme UDP galactose polysaccharide transferase while not affecting the appearance of glycogen phosphorylase. The latter is present in both prestalk and prespore cells.