{"id":26,"date":"2023-06-05T11:57:54","date_gmt":"2023-06-05T10:57:54","guid":{"rendered":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/?page_id=26"},"modified":"2026-02-06T11:18:46","modified_gmt":"2026-02-06T11:18:46","slug":"publications","status":"publish","type":"page","link":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<ul class=\"wp-block-list has-normal-font-size\">\n<li><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.202422673\">Macrocyclic Peptide Probes for Immunomodulatory Protein CD59: Potent Modulators of Bacterial Toxin Activity and Antibody-Dependent Cytotoxicity<\/a><br>Angewandte Chemie Int. Ed., 2025, 64 (27), e202422673<br>J. K. Bickel, A. I. S. Ahmed, A. B. Pidd, R. M. Morgan, <strong>T. E. McAllister<\/strong>, S. Horrell, E. C. Couves, H. Nagaraj, E. J. Bartlett, K. El Omari, A. Kawamura, D. Bubeck*, E. W. Tate*;<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/cb\/d5cb00076a\">Efficient synthesis of <em>O<\/em>-glycosylated amino acids<\/a><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2025\/cb\/d5cb00076a#fn1\"><\/a><br>RSC Chemial Biology 2025,6, 851-856<br><strong>F. J. Frank, R. A. Lawson, T. E. McAllister*<\/strong><\/li>\n\n\n\n<li><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0968089624000117\" data-type=\"link\" data-id=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0968089624000117\">Selective targeting of human TET1 by cyclic peptide inhibitors: Insights from biochemical profiling<\/a><br><em>Bioorganic and Medicinal Chemistry 2024, 99, 117597<\/em><br>K. \u0160imelis, H. Sara\u00e7, E. Salah, K. Nishio, <strong>T.E. M<sup>c<\/sup>Allister<\/strong>, T.P. Corner, A. Tumber, R. Belle, C. J. Schofield, H. Suga, A. Kawamura*<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2023\/sc\/d2sc05944d\" target=\"_blank\" rel=\"noreferrer noopener\">Cyclic peptides target the aromatic cage of a PHD-finger reader domain to modulate epigenetic protein function<\/a><br><em>Chemical Science, 2023, 14 (26), 7136-7146<\/em><br>O. D. Coleman, J. Macdonald, B. Thomson, J. A. Ward, C. J. Stubbs,<strong> T. E. McAllister<\/strong>, S. Clark, S. Amin, Y. Cao, M. I. Abboud, Y. Zhang, H. Sanganee, K. V. M. Huber, T. D. W. Claridge,* A. Kawamura*<\/li>\n\n\n\n<li><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/pep2.24204\" data-type=\"URL\" data-id=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/pep2.24204\" target=\"_blank\" rel=\"noreferrer noopener\">Structural diversity in <em>de novo<\/em> cyclic peptide ligands from genetically encoded library technologies<\/a><br><em>Peptide Science 113 (1), e24204<\/em><br><strong>T. E. M<sup>c<\/sup>Allister*<\/strong>, O. D. Coleman, G. Roper, A. Kawamura*;<\/li>\n\n\n\n<li><a href=\"https:\/\/www.nature.com\/articles\/s41598-020-76307-8\" data-type=\"URL\" data-id=\"https:\/\/www.nature.com\/articles\/s41598-020-76307-8\" target=\"_blank\" rel=\"noreferrer noopener\">Use of Cyclic Peptides to Induce Crystallization \u2013 Case Study with Prolyl Hydroxylase Domain 2<\/a><br><em>Scientific Reports<\/em> <em>2020, 10(1), 21964.<\/em><br>R. Chowdhury, M. I. Abboud, <strong>T. E. M<sup>C<\/sup>Allister<\/strong>, B. Banerji, B. Bhushan, J. L. Sorensen, A. Kawamura, C. J. Schofield*<\/li>\n\n\n\n<li><a href=\"https:\/\/eprint.ncl.ac.uk\/260796\" target=\"_blank\" rel=\"noreferrer noopener\">Non-competitive cyclic peptides for targeting enzyme-substrate complexes<\/a><br><em>Chemical Science 2018, 9(20), 4569-4578.<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, T.-L. Yeh, M. I. Abboud, I. K.H. Leung, E. S. Hookway, O. N. F. King, B. Bhushan, S. J. Williams, R. J. Hopkinson, M. M\u00fcnzel, N. D. Loik, R. Chowdhury, U. Oppermann, T. D. W. Claridge, Y. Goto, H. Suga, C. J. Schofield, A. Kawamura*<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/CC\/C8CC00387D\" target=\"_blank\" rel=\"noreferrer noopener\">2-Oxoglutarate regulates binding of hydroxylated hypoxia-inducible factor to prolyl hydroxylase domain 2<\/a><br><em>Chemical Communications 2018, 54(25), 3130-3133<\/em><br>M. I. Abboud, <strong>T. E. M<sup>c<\/sup>Allister<\/strong>, I. K. H. Leung, R. Chowdhury, C. Jorgensen, C. Domene, J. Mecinovi\u0107, K. Lippl, R. L. Hancock, R. J. Hopkinson, A. Kawamura, T. D. W. Claridge, C. J. Schofield*<\/li>\n\n\n\n<li><a href=\"https:\/\/eprint.ncl.ac.uk\/260799https:\/\/www.nature.com\/articles\/s41598-017-11658-3\" target=\"_blank\" rel=\"noreferrer noopener\">KDM4A regulates HIF-1 levels through H3K9me3<\/a><br><em>Scientific Reports 2017, 7, 11094<\/em><br>G. Dobrynin, <strong>T. E. M<sup>c<\/sup>Allister<\/strong>, K. B. Leszczynska, S. Ramachandran, A. J. Krieg, A. Kawamura, E. M. Hammond*<\/li>\n\n\n\n<li><a href=\"https:\/\/eprint.ncl.ac.uk\/260811\" target=\"_blank\" rel=\"noreferrer noopener\">Recent Progress in Histone Demethylase Inhibitors<\/a><br><em>Journal of Medicinal Chemistry 2016, 59(4), 1308-1329<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, K. S. England, R. J. Hopkinson, P. E. Brennan, A. Kawamura,* C. J. Schofield*<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/OB\/C4OB02587C\" target=\"_blank\" rel=\"noreferrer noopener\">Templating carbohydrate-functionalised polymer-scaffolded dynamic combinatorial libraries with lectins<\/a><br><em>Organic &amp; Biomolecular Chemistry 2015, 13(9), 2756-2761<\/em><br>C. S. Mahon, M. A. Fascione, C. Sakonsinsiri, <strong>T. E. M<sup>c<\/sup>Allister<\/strong>, W. B. Turnbull, D. A. Fulton<\/li>\n\n\n\n<li><a href=\"https:\/\/scholar.google.com\/citations?view_op=view_citation&amp;hl=en&amp;user=akZxopoAAAAJ&amp;sortby=pubdate&amp;citation_for_view=akZxopoAAAAJ:UeHWp8X0CEIC\">A protein\u2010based pentavalent inhibitor of the cholera toxin B\u2010subunit<\/a><br>T. R. Branson, <strong>T. E. M<sup>c<\/sup>Allister<\/strong>, J. Garcia-Hartjes, M. A. Fascione, J. F. Ross, T. Wennekes, H. Zuilhof, W. B. Turnbull*<br>Angewandte Chemie Int. Ed., 2014, 53 (32), 8323\u20138327<\/li>\n\n\n\n<li><a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/cbic.201402090\" target=\"_blank\" rel=\"noreferrer noopener\">Evaluation of the interaction between phosphohistidine analogues and phosphotyrosine binding domains<\/a><br><em>ChemBioChem<\/em> 2014,<em> 15(8), 1088-1091<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, K. A. Horner, M. E. Webb*<\/li>\n\n\n\n<li><a href=\"https:\/\/portlandpress.com\/biochemsoctrans\/article\/41\/4\/1072\/67173\" target=\"_blank\" rel=\"noreferrer noopener\">Prospects for stable analogues of phosphohistidine<\/a><br><em>Biochemical Society Transactions 2013, 41(4), 1072-1077<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, J. J. Hollins, M. E. Webb*<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2012\/ob\/c2ob25517k\" data-type=\"URL\" data-id=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2012\/ob\/c2ob25517k\" target=\"_blank\" rel=\"noreferrer noopener\">Triazole phosphohistidine analogues compatible with the Fmoc-strategy<\/a><br><em>Organic &amp; Biomolecular Chemistry 2012, 10, 4043-4049.<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, M. E. Webb*<\/li>\n\n\n\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2011\/cc\/c0cc04238b\" data-type=\"URL\" data-id=\"https:\/\/pubs.rsc.org\/en\/content\/articlehtml\/2011\/cc\/c0cc04238b\" target=\"_blank\" rel=\"noreferrer noopener\">Fmoc-chemistry of a stable phosphohistidine analogue<\/a><br><em>Chemical Communications 2011, 47(4)<\/em><br><strong>T. E. M<sup>c<\/sup>Allister<\/strong>, M. G. Nix, M. E. Webb*<br><\/li>\n<\/ul>\n\n\n\n<h2 class=\"wp-block-heading\">Links<\/h2>\n\n\n\n<p><a rel=\"noreferrer noopener\" href=\"https:\/\/scholar.google.co.uk\/citations?hl=en&amp;user=akZxopoAAAAJ&amp;view_op=list_works&amp;sortby=pubdate\" data-type=\"URL\" data-id=\"https:\/\/scholar.google.co.uk\/citations?hl=en&amp;user=akZxopoAAAAJ&amp;view_op=list_works&amp;sortby=pubdate\" target=\"_blank\">Google Scholar<\/a><br><a href=\"https:\/\/www.ncl.ac.uk\/nes\/people\/profile\/tommcallister.html\" target=\"_blank\" rel=\"noreferrer noopener\">Newcastle University staff page<\/a><br><\/p>\n","protected":false},"excerpt":{"rendered":"<p>Links Google ScholarNewcastle University staff page<\/p>\n","protected":false},"author":11655,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-26","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/pages\/26","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/users\/11655"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/comments?post=26"}],"version-history":[{"count":9,"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/pages\/26\/revisions"}],"predecessor-version":[{"id":380,"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/pages\/26\/revisions\/380"}],"wp:attachment":[{"href":"https:\/\/blogs.ncl.ac.uk\/tommcallister\/wp-json\/wp\/v2\/media?parent=26"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}