METHODS TO IDENTIFY MACROMOLECULE BINDING AND AGGREGATION PRONE REGIONS IN PROTEINS AND USES THEREFOR

摘要

The present invention provides methods and computational tools based, at least in part, on computer simulations that identify macromolecule binding regions and aggregation prone regions of a protein. Substitutions may then be made in these aggregation prone regions to engineer proteins with enhanced stability and/or a reduced propensity for aggregation. Similarly, substitutions may then be made in these macromolecule binding regions to engineer proteins with altered binding affinity for the macromolecule.

主权项

1. A method of making a protein variant which exhibits a reduced propensity for aggregation and/or an altered binding affinity for a macromolecule, comprising
replacing or deleting at least one amino acid residue within an aggregation prone region and/or a molecular binding region in the protein,wherein the aggregation prone region and/or a molecular binding region is identified using Spatial-Aggregation-Propensity (SAP) scores, wherein the SAP for a particular atom in the protein is calculated by:
(a) providing a computer-readable structural model of the protein; (b) mapping, onto the structural model of the protein the SAP, wherein the SAP is calculated for a particular atom by:
(i) identifying one or more atoms or amino acid residues in a structural model representing the protein, wherein the one or more atoms are within a defined spatial region centered on or within 30 Å of the particular atom or the one or more amino acid residues have at least one atom within a defined spatial region centered on or within 30 Å of the particular atom;(ii) calculating, for each of the one or more atoms in the defined spatial region, a ratio of the solvent accessible area (SAA) of each of the one or more atoms to the SAA of of a corresponding atom in an identical residue which is fully exposed;(iii) multiplying each ratio by the atom hydrophobicity of the one or more atoms; and,(iv) summing the products of step (iii), wherein the sum of the products of step (iii) consists of contributions from the one or more atoms within the defined spatial region; whereby the sum is the SAP for the particular atom; and wherein, optionally, the SAP for the particular atom is calculated by conducting a computational molecular dynamics simulation on the computer-readable structural model of the protein prior to step (i) and repeating steps (i)-(iv), each time conducting a further molecular dynamics simulation at a plurality of time steps, thereby producing multiple sums as in step (iv), and calculating the average of the sums; whereby the calculated average is the SAP for the particular atom; and (c) identifying a region within the protein having a plurality of atoms having a SAP that exceeds a set SAP threshold;wherein the aggregation prone region and/or the molecular binding region comprises the amino acids comprising said plurality of atoms, andwherein, if the amino acid residue is replaced and the region is the aggregation prone region, it is replaced with an amino acid residue which is more hydrophilic, such that the propensity for aggregation of the variant is reduced.