Author

J. D. Lippiat

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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Biophysics· 1 Microbiology· 1 Pharmacology & Toxicology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:cell signaling & trafficking· 1 Assay:cryo-EM· 1 Research Focus:drug response / drug discovery· 1 Assay:electrophysiology· 1 Research Focus:host-pathogen & immune response· 1

Frequent Co-Authors

B. A. Cole· 2 shared N. Pilati· 2 shared S. P. Muench· 2 shared A. C. Kalli· 1 shared A. Whitehouse· 1 shared C. W. G. Fishwick· 1 shared D. J. Hughes· 1 shared H. Carden· 1 shared

Activity by Year

2019-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 19 mutual co-author links

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2 shared papersBiophysics

B. A. Cole

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Author profile →

3 papers

Recent·Most cited

A molecular switch in RCK2 triggers sodium-dependent activation of KNa1.1 (KCNT1) potassium channels.

B. A. Cole, A. C. Kalli, N. Pilati, S. P. Muench, J. D. Lippiat

This paper identifies a molecular switch in the RCK2 domain of KNa1.1 channels that mediates sodium-dependent activation through conformational changes involving specific amino acid residues.

bioRxiv · Sep 28, 2023Biophysics

Kv1.3 induced hyperpolarisation and Cav3.2-mediated calcium entry are required for efficientKaposi's sarcoma-associated herpesvirus lytic replication

H. Carden, M. Dallas, D. J. Hughes, J. D. Lippiat, J. D. Mankouri, A. Whitehouse

The paper identifies Kv1.3 and Cav3.2 ion channels as essential for KSHV lytic replication by promoting Ca2+ influx and NFAT activation.

bioRxiv · Sep 10, 2021 · PreprintMicrobiology

Structure-based identification and characterisation of novel inhibitors of KNa1.1 potassium channels, a stratified target for KCNT1-related epilepsy.

B. A. Cole, R. M. Johnson, H. Dejakaisaya, N. Pilati, C. W. G. Fishwick, S. P. Muench, J. D. Lippiat

This study identifies novel inhibitors of KNa1.1 potassium channels using cryo-EM structures and computational methods, showing improved potency over quinidine for KCNT1-related epilepsy treatment.

bioRxiv · Sep 26, 2019Pharmacology & Toxicology