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Engineered L-asparaginase for cancer therapy

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L-Asparaginases (ASNases) have been used as first line drugs for paediatric Acute Lymphoblastic Leukaemia (ALL) treatment for more than 40 years. Both the Escherichia coli (EcAII) and Erwinia chrysanthemi (ErAII) type II ASNases currently used in the clinics are characterized by high in vivo instability, short half-life and the requirement of several administrations to obtain a pharmacologically active concentration. Moreover, they are sensitive to proteases (cathepsin B and asparagine endopeptidase) that are over-expressed by resistant leukaemia lymphoblasts, thereby impairing drug activity and pharmacokinetics. Herein, we present the biochemical, structural and in vitro antiproliferative characterization of a new EcAII variant, N24S. The mutant shows completely preserved asparaginase and glutaminase activities, long-term storage stability, improved thermal parameters, and outstanding resistance to proteases derived from leukaemia cells. Structural analysis demonstrates a modification in the hydrogen bond network related to residue 24, while Normal Modebased geometric Simulation and Molecular Dynamics predict a general rigidification of the monomer as compared to wild-type. These improved features render N24S a potential alternative treatment to reduce the number of drug administrations in vivo and to successfully address one of the major current challenges of ALL treatment: spontaneous, protease-dependent and immunological inactivation of ASNase.

Reference
Maristella Maggi, Steven D. Mittelman, Jean Hugues Parmentier, Giorgio Colombo,
Massimiliano Meli, Jeannette Marie Whitmire4 D. Scott Merrell, Julian Whitelegge and
Claudia Scotti.
A protease-resistant Escherichia coli asparaginase with outstanding stability and enhanced antileukaemic activity in vitro
Scientific Reports 7:14479 (2017)

Figure
A plot of the RMSD (Å) as a function of simulation time (ns) indicates that the N24S L-asparaginase shows no major structural distortion compared to the wild-type enzyme.

 

 

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