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Antibody RING-Mediated Destruction of Endogenous Proteins

Adel F.M. Ibrahim, Linnan Shen, Michael H. Tatham, David Dickerson, Alan R. Prescott, Naima Abidi, Dimitris P. Xirodimas, Ronald T. Hay

2020Molecular Cell69 citationsDOIOpen Access PDF

Abstract

To understand gene function, the encoding DNA or mRNA transcript can be manipulated and the consequences observed. However, these approaches do not have a direct effect on the protein product of the gene, which is either permanently abrogated or depleted at a rate defined by the half-life of the protein. We therefore developed a single-component system that could induce the rapid degradation of the specific endogenous protein itself. A construct combining the RING domain of ubiquitin E3 ligase RNF4 with a protein-specific camelid nanobody mediates target destruction by the ubiquitin proteasome system, a process we describe as antibody RING-mediated destruction (ARMeD). The technique is highly specific because we observed no off-target protein destruction. Furthermore, bacterially produced nanobody-RING fusion proteins electroporated into cells induce degradation of target within minutes. With increasing availability of protein-specific nanobodies, this method will allow rapid and specific degradation of a wide range of endogenous proteins.

Topics & Concepts

BiologyUbiquitin ligaseUbiquitinProtein degradationEndogenyProteasomeFusion proteinCell biologyUbiquitin-conjugating enzymeRNF4DDB1Molecular biologyAntibodyGeneBiochemistryZinc fingerGeneticsTranscription factorRecombinant DNAUbiquitin and proteasome pathwaysMonoclonal and Polyclonal Antibodies ResearchVirus-based gene therapy research