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利用异源识别结构域重定向E3泛素连接酶以实现靶向蛋白质降解

Redirecting E3 ubiquitin ligases for targeted protein degradation with heterologous recognition domains.

作者信息

Yang Huan, Zheng Ge, Li Grace Y, Alshaye Alia, Orkin Stuart H

机构信息

Department of Pediatrics, Dana Farber/Boston Children's Hospital Cancer and Blood Disorder Center, Boston, Massachusetts, USA; Department of Pediatrics, Harvard Medical School, Boston, Massachusetts, USA.

Department of Pediatrics, Dana Farber/Boston Children's Hospital Cancer and Blood Disorder Center, Boston, Massachusetts, USA.

出版信息

J Biol Chem. 2025 Jan;301(1):108077. doi: 10.1016/j.jbc.2024.108077. Epub 2024 Dec 13.

Abstract

Targeted protein degradation (TPD) mediated by proteolysis targeting chimeras or molecular glues is an emerging therapeutic strategy. Despite greater than 600 E3 ligases and their associated components, a limited number have been deployed in TPD. Those commonly used include cereblon and von Hippel-Lindau tumor suppressor (VHL), which is expressed widely and for which high affinity ligands are available. Limiting TPD to specific cells or tissues would be desirable in many settings. To this goal we have determined the potential of two erythroid cell-enriched E3 ligases, TRIM10 and TRIM58, to degrade a protein of interest, BCL11A, a validated therapeutic target for the β-hemoglobinopathies. We established a general strategy in which heterologous recognition domains replace the PRY-SPRY domain of TRIM10 and TRIM58. Recruitment of TRIM10 or TRIM58 to BCL11A by coiled-coil peptides, nanobodies, or the substrate recognition domain of cereblon led to its degradation. Our findings illustrate a strategy that may be widely useful in evaluating the TPD potential of other E3 ubiquitin ligases and provide a rationale for discovery of ligands for TRIM10 and TRIM58 for erythroid-selective depletion of proteins of interest.

摘要

由靶向蛋白水解嵌合体或分子胶介导的靶向蛋白降解(TPD)是一种新兴的治疗策略。尽管有600多种E3连接酶及其相关成分,但在TPD中应用的数量有限。常用的包括cereblon和von Hippel-Lindau肿瘤抑制因子(VHL),它们广泛表达且有高亲和力配体。在许多情况下,将TPD限制在特定细胞或组织中是可取的。为了实现这一目标,我们确定了两种富含红系细胞的E3连接酶TRIM10和TRIM58降解目标蛋白BCL11A的潜力,BCL11A是β-血红蛋白病的一个经过验证的治疗靶点。我们建立了一种通用策略,其中异源识别结构域取代了TRIM10和TRIM58的PRY-SPRY结构域。通过卷曲螺旋肽、纳米抗体或cereblon的底物识别结构域将TRIM10或TRIM58招募到BCL11A导致其降解。我们的研究结果说明了一种策略,该策略可能在评估其他E3泛素连接酶的TPD潜力方面广泛有用,并为发现用于TRIM10和TRIM58的配体以红系选择性耗尽目标蛋白提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7cdd/11758572/c2fd4f605a1e/gr1.jpg

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