A fragment-based protein interface design algorithm for symmetric assemblies

• Published in: Protein engineering, design and selection Vol. 34
• Main Authors: Laniado, Joshua, Meador, Kyle, Yeates, Todd O
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 15.02.2021
• Subjects: Algorithms; Original; Protein Engineering; Proteins - genetics; Retrospective Studies; Software; secondary structure; algorithms; docking; self-assembly; protein interfaces; symmetry; protein design
• ISSN: 1741-0126; 1741-0134; 1741-0134
• DOI: 10.1093/protein/gzab008

Abstract Theoretical and experimental advances in protein engineering have led to the creation of precisely defined, novel protein assemblies of great size and complexity, with diverse applications. One powerful approach involves designing a new attachment or binding interface between two simpler symmetric oligomeric protein components. The required methods of design, which present both similarities and key differences compared to problems in protein docking, remain challenging and are not yet routine. With the aim of more fully enabling this emerging area of protein material engineering, we developed a computer program, nanohedra, to introduce two key advances. First, we encoded in the program the construction rules (i.e. the search space parameters) that underlie all possible symmetric material constructions. Second, we developed algorithms for rapidly identifying favorable docking/interface arrangements based on tabulations of empirical patterns of known protein fragment-pair associations. As a result, the candidate poses that nanohedra generates for subsequent amino acid interface design appear highly native-like (at the protein backbone level), while simultaneously conforming to the exacting requirements for symmetry-based assembly. A retrospective computational analysis of successful vs failed experimental studies supports the expectation that this should improve the success rate for this challenging area of protein engineering.