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Development of Antibody-Based PROTACs for the Degradation of the Cell-Surface Immune Checkpoint Protein PD-L1

机译:基于抗体的抗体的抗性的抗体,用于细胞表面免疫检查点蛋白PD-L1的降解

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摘要

Targeted protein degradation has emerged as a new paradigm to manipulate cellular proteostasis. Proteolysis-targeting chimeras (PROTACs) are bifunctional small molecules that recruit an E3 ligase to a target protein of interest, promoting its ubiquitination and subsequent degradation. Here, we report the development of antibody-based PROTACs (AbTACs), fully recombinant bispecific antibodies that recruit membrane-bound E3 ligases for the degradation of cell-surface proteins. We show that an AbTAC can induce the lysosomal degradation of programmed death-ligand 1 by recruitment of the membrane-bound E3 ligase RNF43. AbTACs represent a new archetype within the PROTAC field to target cell-surface proteins with fully recombinant biological molecules.
机译:靶向蛋白质降解已成为操纵细胞蛋白质的新范式。蛋白水解靶向嵌合体(Protacs)是双官能的小分子,用于募集E3连接酶至目标蛋白质,促进其泛素化和随后的降解。在这里,我们报告了抗体的抗体(ABTAC)的发展,全重组双特异性抗体,其募集膜结合的E3连接酶用于细胞表面蛋白的降解。我们表明ABTAC可以通过募集膜结合的E3连接酶RNF43来诱导编程死亡配体1的溶酶体降解。 ABTACS代表Pratac领域内的新原型,以靶向细胞表面蛋白质,具有全重组生物分子。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2021年第2期|593-598|共6页
  • 作者单位

    Department of Pharmaceutical Chemistry University of California San Francisco California 94143 United States;

    Department of Pharmaceutical Chemistry University of California San Francisco California 94143 United States;

    Department of Pharmaceutical Chemistry University of California San Francisco California 94143 United States;

    Department of Pharmaceutical Chemistry University of California San Francisco California 94143 United States Cardiovascular Research Institute University of California San Francisco California 94143 United States;

    Department of Pharmaceutical Chemistry University of California San Francisco California 94143 United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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