Unknown

Dataset Information

0

Antibody RING-Mediated Destruction of Endogenous Proteins.


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.

SUBMITTER: Ibrahim AFM 

PROVIDER: S-EPMC7332993 | biostudies-literature | 2020 Jul

REPOSITORIES: biostudies-literature

altmetric image

Publications


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 R  ...[more]

Similar Datasets

2020-05-29 | PXD018113 | Pride
2020-05-28 | PXD016193 | panorama
| S-EPMC10933360 | biostudies-literature
| S-SCDT-10_1038-S44319-024-00063-3 | biostudies-other
| S-EPMC7205596 | biostudies-literature
| S-EPMC8408592 | biostudies-literature
| S-EPMC1820643 | biostudies-literature
| S-EPMC3215076 | biostudies-literature
| S-EPMC5936519 | biostudies-literature
| S-EPMC5785097 | biostudies-literature