Author

M. J. Lista

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Microbiology· 5

Signature Assays, Organisms & Methods

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Approach:experimental assay· 5 Research Focus:host-pathogen & immune response· 5 Organism:human· 5 Assay:proteomics· 4 Research Focus:cell signaling & trafficking· 3 Research Focus:cell type annotation· 2 Research Focus:chromatin & epigenetic regulation· 1 Assay:metagenomics· 1

Frequent Co-Authors

H. Wilson· 4 shared H. Winstone· 4 shared C. M. Swanson· 3 shared D. Kmiec· 3 shared M. Ficarelli· 3 shared R. P. Galao· 3 shared S. J. Neil· 3 shared A. Dyer· 2 shared

Activity by Year

2021-2022 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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4 shared papersMicrobiology

H. Wilson

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Author profile →

5 papers

Recent·Most cited

The P681H mutation in the Spike glycoprotein escapes IFITM restriction and is necessary for type I interferon resistance in the SARS-CoV-2 alpha variant

M. J. Lista, H. Winstone, H. Wilson, A. Dyer, S. Pickering, R. P. Galao, G. De Lorenzo, V. Cowton, W. Furnon, N. M. Suarez, R. Orton, M. Palmirini, A. H. Patel, L. B. Snell, G. Nebbia, , S. J. Neil

This paper shows the P681H mutation in the SARS-CoV-2 alpha variant's Spike protein enables resistance to type I interferon and IFITM proteins, enhancing viral entry and transmission.

bioRxiv · Aug 11, 2022Microbiology

A nuclear export signal in KHNYN required for its antiviral activity evolved as ZAP emerged in tetrapods

M. J. Lista, M. Ficarelli, H. Wilson, D. Kmiec, R. Youle, J. Wanford, H. Winstone, C. Odendall, I. A. Taylor, S. J. Neil, C. M. Swanson

bioRxiv · May 31, 2022Microbiology

Regulation of KHNYN antiviral activity by the extended di-KH domain and nucleo-cytoplasmic trafficking

M. J. Lista, R. P. Galao, M. Ficarelli, D. Kmiec, H. Wilson, H. Winstone, E. R. Morris, H. E. Mischo, J. Wanford, R. Youle, C. Odendall, I. A. Taylor, S. J. Neil, C. Swanson

This paper identifies the extended di-KH and CUBAN domains in KHNYN as critical for its antiviral activity and interaction with ZAP, showing that the CUBAN domain regulates trafficking and abundance.

bioRxiv · Dec 22, 2021 · PreprintMicrobiology

The P681H mutation in the Spike glycoprotein confers Type I interferon resistance in the SARS-CoV-2 alpha (B.1.1.7) variant

M. J. Lista, H. Winstone, H. Wilson, A. Dyer, S. Pickering, R. P. Galao, G. De Lorenzo, V. Cowton, W. Furnon, N. M. Suarez, R. Orton, M. Palmarini, A. H. Patel, L. B. Snell, G. Nebbia, , S. Neil

This study shows the P681H mutation in the SARS-CoV-2 alpha variant's Spike protein confers resistance to Type I interferon, enhancing viral replication by evading innate immune responses.

bioRxiv · Nov 9, 2021 · PreprintMicrobiology

The C-terminal PARP domain of the long ZAP isoform contributes essential effector functions for CpG-directed antiviral activity

D. Kmiec, M. J. Lista, M. Ficarelli, C. Swanson, S. J. D. Neil

This study identifies the C-terminal PARP domain and CaaX box of ZAP-L as essential for CpG-directed antiviral activity by modulating cofactor interactions and subcellular localization.

bioRxiv · Jun 22, 2021 · PreprintMicrobiology