دورية أكاديمية

Cancer cell killing by target antigen engagement with engineered complementary intracellular antibody single domains fused to pro-caspase3.

التفاصيل البيبلوغرافية
العنوان: Cancer cell killing by target antigen engagement with engineered complementary intracellular antibody single domains fused to pro-caspase3.
المؤلفون: Chambers, JS, Brend, T, Rabbitts, TH
المساهمون: Rabbitts, Terence
بيانات النشر: NATURE PORTFOLIO
سنة النشر: 2020
المجموعة: The Institute of Cancer Research (ICR): Publications Repository
مصطلحات موضوعية: Cell Line, Tumor, Humans, Neoplasms, Recombinant Fusion Proteins, Antigens, Neoplasm, Cell Death, Caspase 3, Single-Chain Antibodies, Antineoplastic Agents, Immunological
الوصف: Many tumour causing proteins, such as those expressed after chromosomal translocations or from point mutations, are intracellular and are not enzymes per se amenable to conventional drug targeting. We previously demonstrated an approach (Antibody-antigen Interaction Dependent Apoptosis (AIDA)) whereby a single anti-β-galactosidase intracellular single chain Fv antibody fragment, fused to inactive procaspase-3, induced auto-activation of caspase-3 after binding to the tetrameric β-galactosidase protein. We now demonstrate that co-expressing an anti-RAS heavy chain single VH domain, that binds to mutant RAS several thousand times more strongly than to wild type RAS, with a complementary light chain VL domain, caused programmed cell death (PCD) in mutant RAS expressing cells when each variable region is fused to procaspase-3. The effect requires binding of both anti-RAS variable region fragments and is RAS-specific, producing a tri-molecular complex that auto-activates the caspase pathway leading to cell death. AIDA can be generally applicable for any target protein inside cells by involving appropriate pairs of antigen-specific intracellular antibodies.
نوع الوثيقة: article in journal/newspaper
وصف الملف: Electronic; ?; application/pdf
اللغة: English
تدمد: 2045-2322
العلاقة: Scientific reports, 2019, 9 (1), pp. 8553 - ?; https://repository.icr.ac.uk/handle/internal/3533Test
DOI: 10.1038/s41598-019-44908-7
الإتاحة: https://doi.org/10.1038/s41598-019-44908-7Test
https://repository.icr.ac.uk/handle/internal/3533Test
حقوق: https://creativecommons.org/licenses/by/4.0Test
رقم الانضمام: edsbas.AAA25171
قاعدة البيانات: BASE
الوصف
تدمد:20452322
DOI:10.1038/s41598-019-44908-7