1. Improving the anti-toxin abilities of the CMG2-Fc fusion protein with the aid of computational design.
- Author
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Xi Y, Wu X, Gao L, Shao Y, Peng H, Chen H, Chen H, Hu X, and Yue J
- Subjects
- Antigens, Bacterial chemistry, Antigens, Bacterial genetics, Bacillus anthracis genetics, Bacillus anthracis pathogenicity, Bacterial Toxins antagonists & inhibitors, Bacterial Toxins chemistry, Bacterial Toxins genetics, Humans, Mutation, Missense, Antitoxins chemistry, Antitoxins genetics, Computer Simulation, Immunoglobulin Fc Fragments chemistry, Immunoglobulin Fc Fragments genetics, Immunoglobulin G chemistry, Immunoglobulin G genetics, Models, Molecular, Receptors, Peptide chemistry, Receptors, Peptide genetics
- Abstract
CMG2-Fc is a fusion protein composed of the extracellular domain of capillary morphogenesis protein 2 (CMG2) and the Fc region of human immunoglobulin G; CMG2-Fc neutralizes anthrax toxin and offers protection against Bacillus anthracis challenge. To enhance the efficacy of CMG2-Fc against anthrax toxin, we attempted to engineer a CMG2-Fc with an improved affinity for PA. Using the automatic design algorithm FoldX and visual inspection, we devised two CMG2-Fc variants that introduce mutations in the CMG2 binding interface and improve the computationally assessed binding affinity for PA. An experimental affinity assay revealed that the two variants showed increased binding affinity, and in vitro and in vivo toxin neutralization testing indicated that one of these mutants (CMG2-Fc(E117Q)) has superior activity against anthrax toxin and was suitable for further development as a therapeutic agent for anthrax infections. This study shows that the computational design of the PA binding interface of CMG2 to obtain CMG2-Fc variants with improving anti-toxin abilities is viable. Our results demonstrate that computational design can be further applied to generate other CMG2-Fc mutants with greatly improved therapeutic efficacy.
- Published
- 2014
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