Antibodies play a critical role in the immune system for recognition of foreign intruders. Because of their excellent affinity and specificity, they hav also been exploited as therapeutic molecules and biotechnological components for sensing and assembly. Structures of antibodies in complex with their antigens can yield insight into biological phenomena or drug and disease mechanisms. However, structures of antibodies and antibody-antigen complexes can be difficult, time consuming, and expensive to determine. The proposed research focuses on the computational prediction of the structure of antibodies and antibody-antigen complexes. Computational approaches are particularly important because the repertoire of antibodies in a human patient is far too large for complete structural characterization by experiment. Prior work has isolated the most critical challenges: most of the antibodies in the human repertoire have hypervariable CDR H3 loops longer than that which is predictable using current loop methods;backbone conformational uncertainty and flexibility confound current docking methods;and no current method can quantitatively predict antibody-antigen binding affinities from structure. Thus, the first three aims of the project are to (1) develop new methods to predict the structure of long CDR H3 loops using statistics to identify likely ? turns, (2) develop flexible backbone docking routines using an expanded ensemble approach with a conformational web, and (3) develop methods to quantitatively predict protein-protein binding affinity using improved electrostatics treatments. Finally, the fourth aim will be to (4) use existng and proposed methods to predict structures of antibodies and antibody-antigen complexes for entire polyclonal antibody repertoires. Structures will be predicted for antibody repertoires determined from bone marrow plasma cells of mice immunized against ovalbumin (a food allergen) and enzyme C1s (a therapeutic target for autoimmune diseases and transplant tolerance). Ultimately, these studies will yield insights into immunology, molecular recognition, and design of protein-protein interfaces and vaccines.
Antibodies play a critical role in the immune system for recognition of foreign intruders, and are excellent therapeutic molecules because of their high affinity and specificity. This project investigates computational approaches to determine the three-dimensional structures of antibodies alone and in complex with their target antigens, including specific applications relevant to food allergies and a treatment for transplant rejection autoimmune disorders and inflammatory diseases.
|Koehler Leman, Julia; D'Avino, Andrew R; Bhatnagar, Yash et al. (2018) Comparison of NMR and crystal structures of membrane proteins and computational refinement to improve model quality. Proteins 86:57-74|
|Marze, Nicholas A; Roy Burman, Shourya S; Sheffler, William et al. (2018) Efficient flexible backbone protein-protein docking for challenging targets. Bioinformatics 34:3461-3469|
|Moretti, Rocco; Lyskov, Sergey; Das, Rhiju et al. (2018) Web-accessible molecular modeling with Rosetta: The Rosetta Online Server that Includes Everyone (ROSIE). Protein Sci 27:259-268|
|Jeliazkov, Jeliazko R; Sljoka, Adnan; Kuroda, Daisuke et al. (2018) Repertoire Analysis of Antibody CDR-H3 Loops Suggests Affinity Maturation Does Not Typically Result in Rigidification. Front Immunol 9:413|
|Marze, Nicholas A; Jeliazkov, Jeliazko R; Roy Burman, Shourya S et al. (2017) Modeling oblong proteins and water-mediated interfaces with RosettaDock in CAPRI rounds 28-35. Proteins 85:479-486|
|Santiago-Frangos, Andrew; Jeliazkov, Jeliazko R; Gray, Jeffrey J et al. (2017) Acidic C-terminal domains autoregulate the RNA chaperone Hfq. Elife 6:|
|Koehler Leman, Julia; Mueller, Benjamin K; Gray, Jeffrey J (2017) Expanding the toolkit for membrane protein modeling in Rosetta. Bioinformatics 33:754-756|
|Mathew, Mohit P; Tan, Elaine; Labonte, Jason W et al. (2017) Glycoengineering of Esterase Activity through Metabolic Flux-Based Modulation of Sialic Acid. Chembiochem 18:1204-1215|
|Kilambi, Krishna Praneeth; Gray, Jeffrey J (2017) Structure-based cross-docking analysis of antibody-antigen interactions. Sci Rep 7:8145|
|Alford, Rebecca F; Leaver-Fay, Andrew; Jeliazkov, Jeliazko R et al. (2017) The Rosetta All-Atom Energy Function for Macromolecular Modeling and Design. J Chem Theory Comput 13:3031-3048|
Showing the most recent 10 out of 55 publications