کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
5813810 1556616 2015 9 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
The protective effects and underlying mechanism of an anti-oligomeric Aβ42 single-chain variable fragment antibody
موضوعات مرتبط
علوم زیستی و بیوفناوری علم عصب شناسی علوم اعصاب رفتاری
پیش نمایش صفحه اول مقاله
The protective effects and underlying mechanism of an anti-oligomeric Aβ42 single-chain variable fragment antibody
چکیده انگلیسی


- MO6 is an oligomeric Aβ42-specific scFv antibody.
- MO6 targets oligomeric Aβ42 by conformational recognition and directed induction.
- MO6 effectively reduces the formation of Aβ42 oligomers and immature protofibrils.
- MO6 significantly ameliorate oligomeric Aβ42-induced cytotoxicities.
- MO6 can efficiently pass through the in vitro BBB model.

Oligomeric Aβ42 aggregates have been identified as one of the major neurotoxic components of Alzheimer's disease (AD). Immunotherapy targeted against these Aβ42 aggregates has been proposed as an appropriate therapeutic approach for the treatment of AD. Here, we report an anti-oligomeric Aβ42 single-chain variable fragment (scFv) antibody, named MO6, obtained from the human antibody library of a healthy donor. ScFv MO6 specifically recognized and bound to the oligomeric Aβ42 (Aβ42 oligomers and immature protofibrils; 18-37 kDa), and reduced their levels mainly by blocking their formation, although scFv MO6 also induced disaggregation of Aβ42 aggregates. More importantly, scFv MO6 ameliorated or attenuated Aβ42-induced cytotoxicity and increased cell viability by up to 33%. Furthermore, scFv MO6 efficiently passed through an in vitro blood-brain barrier (BBB) model with a delivery efficiency of 66% after 60 min post-administration. ScFv MO6 is a monovalent antibody with an affinity constant (KD) of 5.2 × 10−6 M for Aβ42 oligomers. Molecular docking simulations of Aβ42 to scFv MO6 revealed that the approach and specific binding of scFv MO6 to oligomeric Aβ42 aggregates was achieved by conformational recognition and directed induction, which resulted in a more dynamic adaptation of Aβ42 to scFv MO6, occurring mainly in the N-terminal (3-4), middle (12-19) and C-terminal (34-42) regions of Aβ42. This binding mode of scFv MO6 to Aβ42 explains its protective effects against oligomeric Aβ42. Our findings may be applied for the design of a smaller antibody specific for Aβ42 oligermers.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Neuropharmacology - Volume 99, December 2015, Pages 387-395
نویسندگان
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