Development of Human Carbonic Anhydrase II Heterobifunctional Degraders.
Conor B O'HerinYuta W MoriuchiTroy A BemisAlysia J KohlbrandMichael D BurkartSeth M CohenPublished in: Journal of medicinal chemistry (2023)
Human carbonic anhydrase II (hCAII) is a metalloenzyme essential to critical physiological processes in the body. hCA inhibitors are used clinically for the treatment of indications ranging from glaucoma to epilepsy. Targeted protein degraders have emerged as a promising means of inducing the degradation of disease-implicated proteins by using the endogenous quality control mechanisms of a cell. Here, a series of heterobifunctional degrader candidates targeting hCAII were developed from a simple aryl sulfonamide fragment. Degrader candidates were functionalized to produce either cereblon E3 ubiquitin ligase (CRBN) recruiting proteolysis targeting chimeras (PROTACs) or adamantyl-based hydrophobic tags (HyTs). Screens in HEK293 cells identified two PROTAC small-molecule degraders of hCA. Optimization of linker length and composition yielded a degrader with sub-nanomolar potency and sustained depletion of hCAII over prolonged treatments. Mechanistic studies suggest that this optimized degrader depletes hCAII through the same mechanism as previously reported CRBN-recruiting heterobifunctional degraders.
Keyphrases
- small molecule
- endothelial cells
- quality control
- cancer therapy
- induced pluripotent stem cells
- induced apoptosis
- pluripotent stem cells
- protein protein
- single cell
- high throughput
- stem cells
- genome wide
- cell therapy
- quantum dots
- cell proliferation
- gene expression
- combination therapy
- endoplasmic reticulum stress
- ionic liquid
- amino acid
- high resolution
- optical coherence tomography