L
Luke Whitesell
Researcher at Massachusetts Institute of Technology
Publications - 75
Citations - 8817
Luke Whitesell is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: HSF1 & Drug resistance. The author has an hindex of 36, co-authored 75 publications receiving 7756 citations. Previous affiliations of Luke Whitesell include University of Arizona & University of Toronto.
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Journal ArticleDOI
Inhibiting mitochondrial phosphate transport as an unexploited antifungal strategy.
Catherine A. McLellan,Benjamin Vincent,Norma V. Solis,Alex K. Lancaster,Lucas B. Sullivan,Cathy L Hartland,Willmen Youngsaye,Scott G. Filler,Scott G. Filler,Luke Whitesell,Susan Lindquist +10 more
TL;DR: Mechanistic characterization of ML316, a thiohydantoin which kills drug-resistant Candida species at nanomolar concentrations through fungal-selective inhibition of the mitochondrial phosphate carrier Mir1, is reported, establishing ML316 as the first Mir1 inhibitor using genetic, biochemical, and metabolomic approaches.
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Endothelial Thermotolerance Impairs Nanoparticle Transport in Tumors.
Alexander F. Bagley,Ruth Scherz-Shouval,Peter A. Galie,Angela Q. Zhang,Jeffrey Wyckoff,Luke Whitesell,Christopher S. Chen,Susan Lindquist,Sangeeta N. Bhatia +8 more
TL;DR: In this article, the authors investigated the ability of one class of heat-generating nanomaterials called plasmonic nanoantennae to enhance tumor transport in a xenograft model of ovarian cancer.
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Rebalancing Protein Homeostasis Enhances Tumor Antigen Presentation.
Alex M. Jaeger,Lauren E. Stopfer,Sunmin Lee,Giorgio Gaglia,Giorgio Gaglia,Demi Sandel,Sandro Santagata,Sandro Santagata,Nan Lin,Jane B. Trepel,Forest M. White,Tyler Jacks,Tyler Jacks,Susan Lindquist,Susan Lindquist,Luke Whitesell +15 more
TL;DR: It is shown that sustained, low-level inhibition of HSP90 both amplifies and diversifies the antigenic repertoire presented by tumor cells on MHC-I molecules through an IFNγ-independent mechanism, which supports reconsideration of the most effective strategy for targeting H SP90 to treat cancers and suggests a practical approach to repurposing current orally bioavailable HSP 90 inhibitors as a new immunotherapeutic strategy.
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FKBP12 contributes to α-synuclein toxicity by regulating the calcineurin-dependent phosphoproteome.
Gabriela Caraveo,Martin Soste,Valentina Cappelleti,Saranna Fanning,Damian B. van Rossum,Luke Whitesell,Yanmei Huang,Yanmei Huang,Chee Yeun Chung,Valeriya Baru,Sofia Zaichick,Paola Picotti,Susan Lindquist +12 more
TL;DR: FKBP12 can endogenously regulate calcineurin activity with therapeutic implications for the treatment of PD by promoting the dephosphorylation of a subset of proteins that contributes to α-syn toxicity.
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Synthesis of Aza-Rocaglates via ESIPT-Mediated (3+2) Photocycloaddition
TL;DR: Synthesis of aza-rocaglates, nitrogen-containing analogues of the rocaglate natural products, is reported, which features ESIPT-mediated (3+2) photocycloaddition of 1-alkyl-2-aryl-3-hydroxyquinolinones with the dipolarophile methyl cinnamate.