tetano
Editor, Senior Moderator
Cell Rep
. 2023 Jan 5;42(1):111951.
doi: 10.1016/j.celrep.2022.111951. Online ahead of print.
Mutational fitness landscape of human influenza H3N2 neuraminidase
Ruipeng Lei[SUP] 1 [/SUP], Andrea Hernandez Garcia[SUP] 1 [/SUP], Timothy J C Tan[SUP] 2 [/SUP], Qi Wen Teo[SUP] 3 [/SUP], Yiquan Wang[SUP] 1 [/SUP], Xiwen Zhang[SUP] 4 [/SUP], Shitong Luo[SUP] 4 [/SUP], Satish K Nair[SUP] 5 [/SUP], Jian Peng[SUP] 6 [/SUP], Nicholas C Wu[SUP] 7 [/SUP]
Affiliations
Abstract
Influenza neuraminidase (NA) has received increasing attention as an effective vaccine target. However, its mutational tolerance is not well characterized. Here, the fitness effects of >6,000 mutations in human H3N2 NA are probed using deep mutational scanning. Our result shows that while its antigenic regions have high mutational tolerance, there are solvent-exposed regions with low mutational tolerance. We also find that protein stability is a major determinant of NA mutational fitness. The deep mutational scanning result correlates well with mutational fitness inferred from natural sequences using a protein language model, substantiating the relevance of our findings to the natural evolution of circulating strains. Additional analysis further suggests that human H3N2 NA is far from running out of mutations despite already evolving for >50 years. Overall, this study advances our understanding of the evolutionary potential of NA and the underlying biophysical constraints, which in turn provide insights into NA-based vaccine design.
Keywords: CP: Molecular biology; deep mutational scanning; evolution; influenza; neuraminidase; protein language model; protein stability; protein structure.
. 2023 Jan 5;42(1):111951.
doi: 10.1016/j.celrep.2022.111951. Online ahead of print.
Mutational fitness landscape of human influenza H3N2 neuraminidase
Ruipeng Lei[SUP] 1 [/SUP], Andrea Hernandez Garcia[SUP] 1 [/SUP], Timothy J C Tan[SUP] 2 [/SUP], Qi Wen Teo[SUP] 3 [/SUP], Yiquan Wang[SUP] 1 [/SUP], Xiwen Zhang[SUP] 4 [/SUP], Shitong Luo[SUP] 4 [/SUP], Satish K Nair[SUP] 5 [/SUP], Jian Peng[SUP] 6 [/SUP], Nicholas C Wu[SUP] 7 [/SUP]
Affiliations
- PMID: 36640354
- DOI: 10.1016/j.celrep.2022.111951
Abstract
Influenza neuraminidase (NA) has received increasing attention as an effective vaccine target. However, its mutational tolerance is not well characterized. Here, the fitness effects of >6,000 mutations in human H3N2 NA are probed using deep mutational scanning. Our result shows that while its antigenic regions have high mutational tolerance, there are solvent-exposed regions with low mutational tolerance. We also find that protein stability is a major determinant of NA mutational fitness. The deep mutational scanning result correlates well with mutational fitness inferred from natural sequences using a protein language model, substantiating the relevance of our findings to the natural evolution of circulating strains. Additional analysis further suggests that human H3N2 NA is far from running out of mutations despite already evolving for >50 years. Overall, this study advances our understanding of the evolutionary potential of NA and the underlying biophysical constraints, which in turn provide insights into NA-based vaccine design.
Keywords: CP: Molecular biology; deep mutational scanning; evolution; influenza; neuraminidase; protein language model; protein stability; protein structure.