Construction of hybrid proteins that migrate retrogradely and transsynaptically into the central nervous system

The nontoxic proteolytic C fragment of tetanus toxin (TTC peptide) has the same ability to bind nerve cells and be retrogradely transported through a synapse as the native toxin, We have investigated its potential use as an in vivo neurotropic carrier, In this work we show that a hybrid protein encoded by the lacZ-TTC gene fusion retains the biological functions of both proteins in vivo-i.e., retrograde transynaptic transport of the TTC fragment and beta-galactosidase enzymatic activity. After intramuscular injection, enzymatic activity could be detected in motoneurons and connected neurons of the brainstem areas, This strategy could be used to deliver a biological activity to neurons from the periphery to the central nervous system, Such a hybrid protein could also be used to map synaptic connections between neural cells.