James Crowe
Faculty Member
Last active: 3/31/2019

Improving Loop Modeling of the Antibody Complementarity-Determining Region 3 Using Knowledge-Based Restraints.

Finn JA, Koehler Leman J, Willis JR, Cisneros A, Crowe JE, Meiler J
PLoS One. 2016 11 (5): e0154811

PMID: 27182833 · PMCID: PMC4868311 · DOI:10.1371/journal.pone.0154811

Structural restrictions are present even in the most sequence diverse portions of antibodies, the complementary determining region (CDR) loops. Previous studies identified robust rules that define canonical structures for five of the six CDR loops, however the heavy chain CDR 3 (HCDR3) defies standard classification attempts. The HCDR3 loop can be subdivided into two domains referred to as the "torso" and the "head" domains and two major families of canonical torso structures have been identified; the more prevalent "bulged" and less frequent "non-bulged" torsos. In the present study, we found that Rosetta loop modeling of 28 benchmark bulged HCDR3 loops is improved with knowledge-based structural restraints developed from available antibody crystal structures in the PDB. These restraints restrict the sampling space Rosetta searches in the torso domain, limiting the φ and ψ angles of these residues to conformations that have been experimentally observed. The application of these restraints in Rosetta result in more native-like structure sampling and improved score-based differentiation of native-like HCDR3 models, significantly improving our ability to model antibody HCDR3 loops.

MeSH Terms (8)

Algorithms Cluster Analysis Complementarity Determining Regions Immunoglobulin Heavy Chains Immunoglobulin Variable Region Models, Molecular Protein Conformation Structure-Activity Relationship

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