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Instruments / Technical Area	Publication Details	Published
I03-Macromolecular Crystallography I04-Macromolecular Crystallography I24-Microfocus Macromolecular Crystallography	Structural and mechanistic insights into the Artemis endonuclease and strategies for its inhibition Yuliana Yosaatmadja , Hannah T. Baddock , Joseph A. Newman , Marcin Bielinski , Angeline E. Gavard , Shubhashish M. M. Mukhopadhyay , Adam a. Dannerfjord , Christopher J. Schofield , Peter j. Mchugh , Opher Gileadi Nucleic Acids Research 44 DOI: 10.1093/nar/gkab693 Diamond Proposal Number(s): [19301] Open Access Show Abstract ▼ Abstract: Artemis (SNM1C/DCLRE1C) is an endonuclease that plays a key role in development of B- and T-lymphocytes and in dsDNA break repair by non-homologous end-joining (NHEJ). Artemis is phosphorylated by DNA-PKcs and acts to open DNA hairpin intermediates generated during V(D)J and class-switch recombination. Artemis deficiency leads to congenital radiosensitive severe acquired immune deficiency (RS-SCID). Artemis belongs to a superfamily of nucleases containing metallo-β-lactamase (MBL) and β-CASP (CPSF-Artemis-SNM1-Pso2) domains. We present crystal structures of the catalytic domain of wildtype and variant forms of Artemis, including one causing RS-SCID Omenn syndrome. The catalytic domain of the Artemis has similar endonuclease activity to the phosphorylated full-length protein. Our structures help explain the predominantly endonucleolytic activity of Artemis, which contrasts with the predominantly exonuclease activity of the closely related SNM1A and SNM1B MBL fold nucleases. The structures reveal a second metal binding site in its β-CASP domain unique to Artemis, which is amenable to inhibition by compounds including ebselen. By combining our structural data with that from a recently reported Artemis structure, we were able model the interaction of Artemis with DNA substrates. The structures, including one of Artemis with the cephalosporin ceftriaxone, will help enable the rational development of selective SNM1 nuclease inhibitors.	Aug 2021
I03-Macromolecular Crystallography	Structure of the helicase core of Werner helicase, a key target in microsatellite instability cancers Joseph A Newman , Angeline E. Gavard , Simone Lieb , Madhwesh C. Ravichandran , Katja Hauer , Patrick Werni , Leonhard Geist , Jark Böttcher , John R Engen , Klaus Rumpel , Matthias Samwer , Mark Petronczki , Opher Gileadi Life Science Alliance 4 DOI: 10.26508/lsa.202000795 Diamond Proposal Number(s): [19301] Open Access Show Abstract ▼ Abstract: Loss of WRN, a DNA repair helicase, was identified as a strong vulnerability of microsatellite instable (MSI) cancers, making WRN a promising drug target. We show that ATP binding and hydrolysis are required for genome integrity and viability of MSI cancer cells. We report a 2.2-Å crystal structure of the WRN helicase core (517–1,093), comprising the two helicase subdomains and winged helix domain but not the HRDC domain or nuclease domains. The structure highlights unusual features. First, an atypical mode of nucleotide binding that results in unusual relative positioning of the two helicase subdomains. Second, an additional β-hairpin in the second helicase subdomain and an unusual helical hairpin in the Zn2+ binding domain. Modelling of the WRN helicase in complex with DNA suggests roles for these features in the binding of alternative DNA structures. NMR analysis shows a weak interaction between the HRDC domain and the helicase core, indicating a possible biological role for this association. Together, this study will facilitate the structure-based development of inhibitors against WRN helicase.	Nov 2020
I03-Macromolecular Crystallography I04-Macromolecular Crystallography	The crystal structure of human forkhead box N1 in complex with DNA reveals the structural basis for forkhead box family specificity Joseph A. Newman , Hazel Aitkenhead , Angeline E. Gavard , Ioanna A Rota , Adam E. Handel , Georg A. Hollander , Opher Gileadi Journal Of Biological Chemistry DOI: 10.1074/jbc.RA119.010365 Diamond Proposal Number(s): [15433] Show Abstract ▼ Abstract: Forkhead box N1 (FOXN1) is a member of the forkhead box family of transcription factors, and plays an important role in thymic epithelial cell differentiation and development. FOXN1 mutations in humans and mice give rise to the “nude” phenotype, which is marked by athymia. FOXN1 belongs to a subset of the FOX family that recognizes an alternative forkhead-like (FHL) consensus sequence (GACGC), that is different from the more widely-recognized forkhead (FKH) sequence RYAAAYA (R = purine, Y = pyrimidine). Here, we present the FOXN1 structure in complex with DNA containing an FHL motif at 1.6 Å resolution, in which the DNA sequence is recognized by a mixture of direct and water-mediated contacts provided by residues in an α-helix inserted in the DNA major groove (the recognition helix). Comparisons with the structure of other FOX family members revealed that the FKH and FHL DNA sequences are bound in two distinct modes, with partially different registers for the protein DNA contacts. We identified a single alternative rotamer within the recognition helix itself as an important determinant of DNA specificity and found protein sequence features in the recognition helix that could be used to predict the specificity of other FOX family members. Finally, we demonstrate that the C-terminal region of FOXN1 is required for high-affinity DNA binding and that FOXN1 has a significantly reduced affinity for DNA that contains 5’-methylcytosine, which may have implications for the role of FOXN1 in thymic involution.	Dec 2019

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