GPX4 in cell death, autophagy, and disease
ABSTRACT Selenoprotein GPX4 (glutathione peroxidase 4), originally known as PHGPX
(phospholipid hydroperoxide glutathione peroxidase), is the main oxidoreductase in the use …
(phospholipid hydroperoxide glutathione peroxidase), is the main oxidoreductase in the use …
Targeting GPX4 in human cancer: Implications of ferroptosis induction for tackling cancer resilience
J Lee, JL Roh - Cancer Letters, 2023 - Elsevier
Cancer metabolic alterations have been emphasized to protect cancer cells from cell death.
The metabolic reprogramming toward a mesenchymal state makes cancer cells resistant to …
The metabolic reprogramming toward a mesenchymal state makes cancer cells resistant to …
Rational chemical design of molecular glue degraders
ES Toriki, JW Papatzimas, K Nishikawa… - ACS central …, 2023 - ACS Publications
Targeted protein degradation with molecular glue degraders has arisen as a powerful
therapeutic modality for eliminating classically undruggable disease-causing proteins …
therapeutic modality for eliminating classically undruggable disease-causing proteins …
[HTML][HTML] Proteomic discovery of chemical probes that perturb protein complexes in human cells
Most human proteins lack chemical probes, and several large-scale and generalizable small-
molecule binding assays have been introduced to address this problem. How compounds …
molecule binding assays have been introduced to address this problem. How compounds …
CysDB: a human cysteine database based on experimental quantitative chemoproteomics
Cysteine chemoproteomics provides proteome-wide portraits of the ligandability or potential"
druggability" for thousands of cysteine residues. Consequently, these studies are facilitating …
druggability" for thousands of cysteine residues. Consequently, these studies are facilitating …
Thiomethyltetrazines Are Reversible Covalent Cysteine Warheads Whose Dynamic Behavior can be “Switched Off” via Bioorthogonal Chemistry Inside Live Cells
Electrophilic small molecules that can reversibly modify proteins are of growing interest in
drug discovery. However, the ability to study reversible covalent probes in live cells can be …
drug discovery. However, the ability to study reversible covalent probes in live cells can be …
[HTML][HTML] Chemoproteomics-enabled discovery of a covalent molecular glue degrader targeting NF-κB
EA King, Y Cho, NS Hsu, D Dovala, JM McKenna… - Cell chemical …, 2023 - cell.com
Targeted protein degradation has arisen as a powerful therapeutic modality for degrading
disease targets. While proteolysis-targeting chimera (PROTAC) design is more modular, the …
disease targets. While proteolysis-targeting chimera (PROTAC) design is more modular, the …
Withaferin A: a dietary supplement with promising potential as an anti-tumor therapeutic for cancer treatment-pharmacology and mechanisms
Z Xing, A Su, L Mi, Y Zhang, T He, Y Qiu… - Drug Design …, 2023 - Taylor & Francis
Cancer, as the leading cause of death worldwide, poses a serious threat to human health,
making the development of effective tumor treatments a significant challenge. Natural …
making the development of effective tumor treatments a significant challenge. Natural …
Activity‐Based Protein Profiling–Finding General Solutions to Specific Problems
BF Cravatt - Israel journal of chemistry, 2023 - Wiley Online Library
In this retrospective/perspective, I will share thoughts on developing and applying the activity‐
based protein profiling (ABPP) technology, an endeavor that has consumed much of our …
based protein profiling (ABPP) technology, an endeavor that has consumed much of our …
AzidoTMT enables direct enrichment and highly multiplexed quantitation of proteome-wide functional residues
TP Ma, A Izrael-Tomasevic, R Mroue… - Journal of Proteome …, 2023 - ACS Publications
Recent advances in targeted covalent inhibitors have aroused significant interest for their
potential in drug development for difficult therapeutic targets. Proteome-wide profiling of …
potential in drug development for difficult therapeutic targets. Proteome-wide profiling of …