The goal of the proposed research is to develop an improved approach for the treatment of blood cancers that utilizes human enzymes rather than bacterial enzymes. Currently, a mainstay treatment of such cancers includes the administration of a bacterial enzyme called asparaginase. The activity of this enzyme is to hydrolyze the amino acid asparagine to aspartic acid and ammonia. Certain blood cancers are dependent on the extracellular pool of asparagine. Administration of asparaginase depletes this source, depriving the cancer cells of a vital amino acid, and ultimately induces cell death (apoptosis). Because all currently approved preparations of asparaginases are of bacterial origin, a substantial proportion of patients have an immune response against the enzyme - a reaction that can be deadly. Moreover, the generated anti-bacterial asparaginase antibodies clear the enzyme from circulation, thereby eliminating its anticancer potential and preventing further administration of the drug. A further complication is due to the undesired glutaminase activity of bacterial asparaginases, which is a source of toxicity of this treatment. We propose to replace the bacterial enzymes with human asparaginases. This will abolish the immune response. We will also engineer the human enzymes to be devoid of glutaminase activity, thereby eliminating this cause of toxicity. The wild-type versions of human asparaginases are not suitable for replacing the bacterial enzymes since their Km value is in the millimolar range, yet the concentration of asparagine in blood is only about 50 micromolar. Indeed, the bacterial enzymes used in the clinic, from E. coli and Erwinia, have a low Km value for asparagine. The research in this proposal delineates a strategy to engineer human asparaginases to have this vital property of low Km with asparagine.
In Aim 1 we will study the structure/function properties of two human asparaginases. We will incorporate structural, biochemical, kinetic, and mutagenesis approaches in this part of the proposal. The data from Aim 1 will inform the engineering studies of Aim 2. The strategy is to introduce mutations that result in (i) lowering of the asparagine Km value to the micromolar range, (ii) an enzyme devoid of glutaminase activity, and (iii) improved thermo-stability. The latter is to increase the circulation half-life of the enzyme in the patientsso that the asparaginase activity is long lasting. An additional novel aspect of Aim 2 is the linking f the human asparaginase to human serum albumin (HSA). Since HSA has a circulation half-life of ~20 days, we hypothesize that the fusion HSA- asparaginase will have increased circulation half-life relative to the free enzyme. This will significantly aid the clinical use of this drug, ad will result in more persistent asparagine depletion.
Aim 3 will test the cell-killing power of the engineered asparaginases in cell culture, and the stability of the enzymes in plasma. The purpose of Aim 3 is to ready the engineered human asparaginases for clinical trials. Adults treated with the bacterial asparaginases exhibit a more intense immune response compared to pediatric patients. Hence, the less immunogenic enzymes developed here will especially be beneficial to this patient population. This makes this proposal especially relevant to the treatment of veterans.
This research will develop improved treatments for blood cancers. Blood cancers represent 2 of the10 most prevalent cancers in the United States (i.e. leukemia and non-Hodgkin lymphoma) and strike adults as well as children across the US population - including military families. Lack of effective treatment is particularly relevant to military families given the association between blood cancers and exposure to chemical and biological agents. Exposure to such agents puts veterans of the Vietnam War and the two Gulf Wars at higher risk of blood cancers such as lymphoma, chronic lymphocytic leukemia, and multiple myeloma. Current treatment of several blood cancers utilizes bacterial enzymes. Unfortunately, because the body recognizes these bacterial enzymes as foreign, they trigger complicating immune responses. We will develop versions of human enzymes to replace the currently used bacterial enzymes, resulting in safer treatment for patients because they will not trigger an immune response, while being efficacious in killing the cancer cells.
|Nguyen, Hien Anh; Su, Ying; Zhang, Jenny Y et al. (2018) A Novel l-Asparaginase with low l-Glutaminase Coactivity Is Highly Efficacious against Both T- and B-cell Acute Lymphoblastic Leukemias In Vivo. Cancer Res 78:1549-1560|
|Nguyen, Hien Anh; Durden, Donald L; Lavie, Arnon (2017) The differential ability of asparagine and glutamine in promoting the closed/active enzyme conformation rationalizes the Wolinella succinogenes L-asparaginase substrate specificity. Sci Rep 7:41643|
|Rigouin, Coraline; Nguyen, Hien Anh; Schalk, Amanda M et al. (2017) Discovery of human-like L-asparaginases with potential clinical use by directed evolution. Sci Rep 7:10224|
|Nguyen, Hien Anh; Su, Ying; Lavie, Arnon (2016) Structural Insight into Substrate Selectivity of Erwinia chrysanthemi L-asparaginase. Biochemistry 55:1246-53|
|Nguyen, Hien Anh; Su, Ying; Lavie, Arnon (2016) Design and Characterization of Erwinia Chrysanthemi l-Asparaginase Variants with Diminished l-Glutaminase Activity. J Biol Chem 291:17664-76|
|Schalk, Amanda M; Antansijevic, Aleksandar; Caffrey, Michael et al. (2016) Experimental Data in Support of a Direct Displacement Mechanism for Type I/II L-Asparaginases. J Biol Chem 291:5088-100|