A grand challenge in biomolecular research is to rationally design antibodies that bind to target antigens with high affinity and specificity. The goal of this proposal is to elucidate principles for designing the complementarity-determining regions (CDRs) of antibody fragments to mediate recognition of aggregated proteins with conformational and sequence specificity. Our proposal is based on our recent discovery that single-domain antibodies can be designed to recognize A42 oligomers and fibrils using the same molecular interactions mediating Aaggregation associated with Alzheimer's disease (Perchiacca et al., PNAS, 2012). We find that hydrophobic A peptides can be grafted into a single CDR loop, and the resulting Grafted AMyloid-Motif AntiBODIES (gammabodies) bind to A oligomers and fibrils with nanomolar affinity. Based on these discoveries, we posit that additional A peptides capable of mediating gammabody binding can be predicted based on their relative amyloidogenicity. We also hypothesize that the binding affinity of gammabodies will be maximal at small to intermediate CDR lengths that are sufficiently long to display A self-recognition peptides but not long enough to disfavor binding due to increased entropy. In addition, we posit that our design approach is not limited to Aand can be extended to other amyloidogenic polypeptides, including IAPP (type 2 diabetes) and ?-synuclein (Parkinson's disease). Finally, we hypothesize that even higher-affinity gammabodies can be designed by grafting multiple amyloidogenic peptides into anti-parallel CDRs that are oriented in the same manner as the corresponding peptides at the growing (templating) ends of fibrils. Therefore, in Aim 1, we propose to determine how the length and sequence of CDR3 impacts the binding affinity and specificity for two A gammabodies (A15-24 and A33-42). Then, in Aim 2, we propose to evaluate our predictions of additional A peptides that mediate gammabody binding to Aaggregates when grafted into CDR3. Next, in Aim 3, we propose to extend the analysis performed in Aims 1 and 2 to evaluate our predictions of peptide segments from two other amyloid-forming polypeptides (?-synuclein and IAPP) that mediate gammabody binding to their corresponding aggregated conformers when grafted into CDR3. Finally, in Aim 4, we propose to evaluate whether the affinity of the Aand IAPP gammabodies developed in Aims 1-3 can be increased by grafting two different amyloidogenic peptides into anti-parallel CDRs to match the orientation of the corresponding peptides at the growing ends of fibrils. A significant outcome of our studies will be the elucidation of how self-complementary, amyloidogenic peptides can be used to mediate antibody-antigen recognition. We expect that our findings will lead to rules for designing of similar single- and multidomain antibodies with specificity for diverse amyloidogenic proteins, including those linked to human aggregation disorders such as Huntington's and prion diseases.
Antibodies that recognize toxic protein particles could be used to prevent or treat diseases such as Alzheimer's or prion diseases. We aim to understand how to rationally design antibodies that specifically recognize toxic protein particles.
|Tiller, Kathryn E; Chowdhury, Ratul; Li, Tong et al. (2017) Facile Affinity Maturation of Antibody Variable Domains Using Natural Diversity Mutagenesis. Front Immunol 8:986|
|Tiller, Kathryn E; Li, Lijuan; Kumar, Sandeep et al. (2017) Arginine mutations in antibody complementarity-determining regions display context-dependent affinity/specificity trade-offs. J Biol Chem 292:16638-16652|
|Zhao, Jing; Huvent, Isabelle; Lippens, Guy et al. (2017) Glycan Determinants of Heparin-Tau Interaction. Biophys J 112:921-932|
|Julian, Mark C; Li, Lijuan; Garde, Shekhar et al. (2017) Efficient affinity maturation of antibody variable domains requires co-selection of compensatory mutations to maintain thermodynamic stability. Sci Rep 7:45259|
|Osborne, Danielle M; Fitzgerald, Dennis P; O'Leary, Kelsey E et al. (2016) Intrahippocampal administration of a domain antibody that binds aggregated amyloid-? reverses cognitive deficits produced by diet-induced obesity. Biochim Biophys Acta 1860:1291-8|
|Nilvebrant, Johan; Tessier, Peter M; Sidhu, Sachdev S (2016) Engineered Autonomous Human Variable Domains. Curr Pharm Des 22:6527-6537|
|Lee, Christine C; Julian, Mark C; Tiller, Kathryn E et al. (2016) Design and Optimization of Anti-amyloid Domain Antibodies Specific for ?-Amyloid and Islet Amyloid Polypeptide. J Biol Chem 291:2858-73|
|Julian, Mark C; Lee, Christine C; Tiller, Kathryn E et al. (2015) Co-evolution of affinity and stability of grafted amyloid-motif domain antibodies. Protein Eng Des Sel 28:339-50|
|Tiller, Kathryn E; Tessier, Peter M (2015) Advances in Antibody Design. Annu Rev Biomed Eng 17:191-216|
|Geng, Steven B; Cheung, Jason K; Narasimhan, Chakravarthy et al. (2014) Improving monoclonal antibody selection and engineering using measurements of colloidal protein interactions. J Pharm Sci 103:3356-3363|