{"title":"Fluorescence polarization binding assays for the E3 ligase FEM1C.","authors":"Emma K Seipp, Rong Huang","doi":"10.1016/bs.mie.2025.06.002","DOIUrl":null,"url":null,"abstract":"<p><p>Feminization-1 homolog C (FEM1C) is a substrate-recognition component of the Cullin 2-RING E3 ubiquitin ligases (CRL2), selectively binding the C-degron containing arginine-terminated motifs to mediate proteasomal degradation of target proteins. Owing to its wide expression, FEM1C holds promise for targeted protein degradation. This chapter describes fluorescence polarization-based binding assays for FEM1C, as well as preparation of the required reagents including the recombinant protein and fluorescent probe. These methods can be applied to identify ligands for FEM1C or adapted for other E3 ligases, facilitating the development of new handles for targeted protein degradation.</p>","PeriodicalId":18662,"journal":{"name":"Methods in enzymology","volume":"719 ","pages":"347-362"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Methods in enzymology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1016/bs.mie.2025.06.002","RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/11 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"Biochemistry, Genetics and Molecular Biology","Score":null,"Total":0}
引用次数: 0
Abstract
Feminization-1 homolog C (FEM1C) is a substrate-recognition component of the Cullin 2-RING E3 ubiquitin ligases (CRL2), selectively binding the C-degron containing arginine-terminated motifs to mediate proteasomal degradation of target proteins. Owing to its wide expression, FEM1C holds promise for targeted protein degradation. This chapter describes fluorescence polarization-based binding assays for FEM1C, as well as preparation of the required reagents including the recombinant protein and fluorescent probe. These methods can be applied to identify ligands for FEM1C or adapted for other E3 ligases, facilitating the development of new handles for targeted protein degradation.
期刊介绍:
The critically acclaimed laboratory standard for almost 50 years, Methods in Enzymology is one of the most highly respected publications in the field of biochemistry. Each volume is eagerly awaited, frequently consulted, and praised by researchers and reviewers alike. Now with over 500 volumes the series contains much material still relevant today and is truly an essential publication for researchers in all fields of life sciences, including microbiology, biochemistry, cancer research and genetics-just to name a few. Five of the 2013 Nobel Laureates have edited or contributed to volumes of MIE.