Chondroitin sulfate proteoglycans inhibit regeneration, neuroprotection, and plasticity following spinal cord injury. The development of a second-generation chondroitinase ABC enzyme, capable of being secreted from mammalian cells (mChABC), has facilitated the functional recovery of animals following severe spinal trauma. The genetically modified enzyme has been shown to efficiently break down the inhibitory extracellular matrix surrounding cells at the site of injury, while facilitating cellular integration and axonal growth. However, the activity profile of the enzyme in relation to the original bacterial chondroitinase (bChABC) has not been determined. Here, we characterize the activity profile of mChABC and compare it to bChABC, both enzymes having been maintained under physiologically relevant conditions for the duration of the experiment. We show that this genetically modified enzyme can be secreted reliably and robustly in high yields from a mammalian cell line. The modifications made to the cDNA of the enzyme have not altered the functional activity of mChABC compared to bChABC, ensuring that it has optimal activity on chondroitin sulfate-A, with an optimal pH at 8.0 and temperature at 37 °C. However, mChABC shows superior thermostability compared to bChABC, ensuring that the recombinant enzyme operates with enhanced activity over a variety of physiologically relevant substrates and temperatures compared to the widely used bacterial alternative without substantially altering its kinetic output. The determination that mChABC can function with greater robustness under physiological conditions than bChABC is an important step in the further development of this auspicious treatment strategy toward a clinical application.

Centre for Reconstructive Neuroscience Institute of Experimental Medicine Czech Academy of Sciences Videnska 1083 14220 Prague 4 Czech Republic

Department of Clinical Neurosciences John van Geest Centre for Brain Repair University of Cambridge Cambridge CB2 0PY U K

Department of Physiology Development and Neuroscience University of Cambridge Cambridge CB2 0PY U K

School of Biomedical Sciences Faculty of Biological Sciences University of Leeds Leeds LS2 9JT U K

Wolfson Centre for Age Related Diseases Institute of Psychiatry Psychology and Neuroscience King's College London Guy's Campus London Bridge London SE1 1UL U K

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