[ASAP] Redefining the Scope of Targeted Protein Degradation: Translational Opportunities in Hijacking the Autophagy–Lysosome Pathway
Redefining the Scope of Targeted Protein Degradation: Translational Opportunities in Hijacking the Autophagy–Lysosome Pathway
https://pubs.acs.org/na101/home/literatum/publisher/achs/journals/content/bichaw/0/bichaw.ahead-of-print/acs.biochem.1c00330/20210927/images/medium/bi1c00330_0002.gif
Biochemistry
DOI: 10.1021/acs.biochem.1c00330
http://feeds.feedburner.com/~r/acs/bichaw/~4/joOGR6eQNhs
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nmrlearner
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09-27-2021 10:14 PM
[NMR paper] From medium to endoplasmic reticulum: Tracing anticancer phenolato titanium(IV) complex by (19)F NMR detection
From medium to endoplasmic reticulum: Tracing anticancer phenolato titanium(IV) complex by (19)F NMR detection
Titanium(IV) complexes of diaminobis(phenolato)-bis(alkoxo) ligands are promising anticancer drugs, showing marked in-vivo efficacy with no toxic side-effects in mice, hence, it is of interest to elucidate their mechanism of action. Herein, we employed a fluoro-substituted derivative, FenolaTi, for mechanistic analysis of the active species and its cellular target by quantitative ^(19)F NMR detection to reveal its biodistribution and reactivity in extracellular and intracellular...
nmrlearner
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05-30-2021 06:35 AM
[NMR paper] Helix Fraying and Lipid-Dependent Structure of a Short Amphipathic Membrane-Bound Peptide Revealed by Solid-State NMR.
Helix Fraying and Lipid-Dependent Structure of a Short Amphipathic Membrane-Bound Peptide Revealed by Solid-State NMR.
http://www.bionmr.com//www.ncbi.nlm.nih.gov/corehtml/query/egifs/http:--pubs.acs.org-images-pubmed-acspubs.jpg Related Articles Helix Fraying and Lipid-Dependent Structure of a Short Amphipathic Membrane-Bound Peptide Revealed by Solid-State NMR.
J Phys Chem B. 2018 06 14;122(23):6236-6250
Authors: Strandberg E, Grau-Campistany A, Wadhwani P, Bürck J, Rabanal F, Ulrich AS
Abstract
The amphipathic ?-helical...
nmrlearner
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04-19-2019 10:31 AM
[NMR paper] Elucidating ligand-bound structures of membrane proteins using solid-state NMR spectroscopy.
Elucidating ligand-bound structures of membrane proteins using solid-state NMR spectroscopy.
Related Articles Elucidating ligand-bound structures of membrane proteins using solid-state NMR spectroscopy.
Curr Opin Struct Biol. 2019 Mar 20;57:103-109
Authors: Elkins MR, Hong M
Abstract
Magic-angle-spinning (MAS) solid-state NMR spectroscopy is a versatile technique to elucidate functionally important protein-ligand interactions in lipid membranes. Here, we review recent solid-state NMR studies of membrane protein interactions with...
[NMR paper] Solution NMR Studies on the Orientation of Membrane-Bound Peptides and Proteins by Paramagnetic Probes.
Solution NMR Studies on the Orientation of Membrane-Bound Peptides and Proteins by Paramagnetic Probes.
Solution NMR Studies on the Orientation of Membrane-Bound Peptides and Proteins by Paramagnetic Probes.
Molecules. 2013;18(7):7407-7435
Authors: Schrank E, Wagner GE, Zangger K
Abstract
Many peptides and proteins are attached to or immersed in a biological membrane. In order to understand their function not only the structure but also their topology in the membrane is important. Solution NMR spectroscopy is one of the most often...