Cover image artwork for Mullowney, M. W.; Fiebig, A.; Schnizlein, M. K.; McMillin, M.; Koval, J.; Rubin, D.; Dalal, S.; Sogin, M.L.; Chang, E. B.; Sidebottom, A. M.; Crosson, S. Microbially-catalyzed conjugation of GABA and tyramine to bile acids. J. Bacteriol. 2024, 206 , e00426–23.
Animated version of cover image artwork for McGee, J.P.; Melani, R.D.; Yip, P.F.; Senko, M.W.; Compton, P.D.; Kafader, J.O.;Kelleher, N.L. Isotopic Resolution of Protein Complexes up to 466 kDa Using Individual Ion Mass Spectrometry. Anal. Chem.2020. 93, 2723-2727.
A totally fake, yet plausible, NRPS biosynthesis of "fakeomycin" featuring a cyclization (Cy) domain. May, 2020.
Cover image artwork (and table of contents graphic) for Kafader, J.O.; Durbin, K.R.; Melani, R.D.; Des Soye B.J.; Schachner, L.F.; Senko, M.W.; Compton, P.D.; Kelleher, N.L. Individual Ion Mass Spectrometry Enhances the Sensitivity and Sequence Coverage of Top Down Mass Spectrometry. J. Proteome Res.2020, 19, 1346–1350.
Journal cover and media release artwork for Kafader, J.O.; Melani, R.D.; Durbin, K.R.; Ikwuagwu, B.; Early, B.P.; Fellers, R.T.; Beu, S.C.; Zabrouskov, V.; Makarov, A.A.; Maze, J.T.; Shinholt, D.L.; Yip, P.F.; Tullman-Ercek, D.; Senko, M.W.; Compton, P.D.; Kelleher, N.L. Multiplexed Single Ion Mass Spectrometry Improves Measurement of Proteoforms and Their Complexes. Nat. Methods.2020,17, 391–394. Also featured in Phys.org, Drug Target Review, AZoOptics, Northwestern Now, and Northwestern Chemistry of Life Processes (CLP).
Micromonospora sp. G039 cultured in the shape of the isopimara-2-one-3-ol-8,15-diene chemical structure. From: Mullowney, M.W.; Ó hAinmhire, E.; Tanouye, U.; Burdette, J.E.; Pham, V.C.; Murphy, B.T. A Pimarane Diterpene and Cytotoxic Angucyclines from a Marine-Derived Micromonospora sp. in Vietnam’s East Sea. Mar. Drugs. 2015, 13, 5815-27.
Cover image artwork for Mullowney, M.W.; McClure, R.; Robey, M.; Kelleher, N.L..; Thomson, R.J. Natural products from biosynthetic assembly lines terminating in thioester reductases. Nat. Prod. Rep. 2018, 35, 847-78.
A fractionated extract from fermentation of Streptomyces sp. F001, which contains diazaquinomycins A-F (red), and akashins (cyan). From: Mullowney, M.W.; Ó hAinmhire, E.; Shaikh, A.; Wei, X.; Tanouye, U.; Santarsiero, B.D.; Burdette, J.E.; Murphy, B.T. Diazaquinomycins E–G, novel diaza-anthracene analogs from a marine-derived Streptomyces sp. Mar. Drugs.2014, 12, 3574-86.
A fractionated extract from fermentation of Streptomyces sp. F001, which contains diazaquinomycins A-F (red), and akashins (cyan). From: Mullowney, M.W.; Ó hAinmhire, E.; Shaikh, A.; Wei, X.; Tanouye, U.; Santarsiero, B.D.; Burdette, J.E.; Murphy, B.T. Diazaquinomycins E–G, novel diaza-anthracene analogs from a marine-derived Streptomyces sp. Mar. Drugs.2014, 12, 3574-86.