PEP-Patch: Electrostatics in Protein-Protein Recognition, Specificity, and Antibody Developability

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Abstract

The electrostatic properties of proteins arise from the number and distribution of polar and charged residues. Electrostatic interactions in proteins play a critical role in numerous processes such as molecular recognition, protein solubility, viscosity, and antibody developability. Thus, characterizing and quantifying electrostatic properties of a protein are prerequisites for understanding these processes. Here, we present PEP-Patch, a tool to visualize and quantify the electrostatic potential on the protein surface in terms of surface patches, denoting separated areas of the surface with a common physical property. We highlight its applicability to elucidate protease substrate specificity and antibody-antigen recognition and predict heparin column retention times of antibodies as an indicator of pharmacokinetics.

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Hoerschinger, V. J., Waibl, F., Pomarici, N. D., Loeffler, J. R., Deane, C. M., Georges, G., … Liedl, K. R. (2023). PEP-Patch: Electrostatics in Protein-Protein Recognition, Specificity, and Antibody Developability. Journal of Chemical Information and Modeling, 63(22), 6964–6971. https://doi.org/10.1021/acs.jcim.3c01490

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