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Eric Spooner
Researcher at Massachusetts Institute of Technology
Publications - 45
Citations - 7353
Eric Spooner is an academic researcher from Massachusetts Institute of Technology. The author has contributed to research in topics: Ubiquitin & Deubiquitinating enzyme. The author has an hindex of 30, co-authored 45 publications receiving 6729 citations.
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PRAS40 is an insulin-regulated inhibitor of the mTORC1 protein kinase.
Yasemin Sancak,Carson C. Thoreen,Timothy R. Peterson,Robert A. Lindquist,Seong A. Kang,Eric Spooner,Steven A. Carr,David M. Sabatini,David M. Sabatini +8 more
TL;DR: It is proposed that the relative strengths of the rheb- and PRAS40-mediated inputs to m TORC1 set overall pathway activity and that insulin activates mTORC1 through the coordinated regulation of both.
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Reversal of Histone Lysine Trimethylation by the JMJD2 Family of Histone Demethylases
Johnathan R. Whetstine,Amanda C. Nottke,Fei Lan,Maite Huarte,Sarit Smolikov,Zhongzhou Chen,Eric Spooner,En Li,Gongyi Zhang,Monica P. Colaiácovo,Yang Shi +10 more
TL;DR: The finding that this family of demethylases generates different methylated states at the same lysine residue provides a mechanism for fine-tuning histone methylation.
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Sortagging: a versatile method for protein labeling
TL;DR: sortagging (sortase-mediated transpeptidation) is a versatile chemoenzymatic system for site-specific labeling of proteins with small (<2 kDa) probes and is applied to proteins in vitro and on the surface of living cells.
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Haploid Genetic Screens in Human Cells Identify Host Factors Used by Pathogens
Jan E. Carette,Carla P. Guimaraes,Malini Varadarajan,Annie S. Park,Irene Wuethrich,Alzbeta Godarova,Maciej Kotecki,Brent H. Cochran,Eric Spooner,Hidde L. Ploegh,Thijn R. Brummelkamp +10 more
TL;DR: Using insertional mutagenesis to develop a screening method to generate null alleles in a human cell line haploid for all chromosomes except chromosome 8, host factors essential for infection with influenza and genes encoding important elements of the biosynthetic pathway of diphthamide, which are required for the cytotoxic effects ofdiphtheria toxin and exotoxin A are identified.
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Proteolytic cleavage in an endolysosomal compartment is required for activation of Toll-like receptor 9
TL;DR: Although cathepsin L generated the requisite TLR9 cleavage products in a cell-free in vitro system, several proteases influenced TLR7 cleavage in intact cells, and Lysosomal proteolysis contributes to innate immunity by facilitating specific cleavage ofTLR9.