GPX4 in cell death, autophagy, and disease

Y Xie, R Kang, DJ Klionsky, D Tang - Autophagy, 2023 - Taylor & Francis
ABSTRACT Selenoprotein GPX4 (glutathione peroxidase 4), originally known as PHGPX
(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 …

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 …

[HTML][HTML] Proteomic discovery of chemical probes that perturb protein complexes in human cells

MR Lazear, JR Remsberg, MG Jaeger, K Rothamel… - Molecular cell, 2023 - cell.com
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 …

CysDB: a human cysteine database based on experimental quantitative chemoproteomics

LM Boatner, MF Palafox, DK Schweppe… - Cell Chemical …, 2023 - cell.com
Cysteine chemoproteomics provides proteome-wide portraits of the ligandability or potential"
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

AM Tallon, Y Xu, GM West, CW Am Ende… - Journal of the American …, 2023 - ACS Publications
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 …

[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 …

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 …

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 …

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 …