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Si us plau utilitzeu sempre aquest identificador per citar o enllaçar aquest document: https://hdl.handle.net/2445/110867
The antigen-binding fragment of human gamma immunoglobulin prevents amyloid beta-peptide folding into beta-sheet to form oligomers
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The amyloid beta-peptide (Abeta) plays a leading role in
Alzheimer's disease (AD) physiopathology. Even though monomeric
forms of Abeta are harmless to cells, Abeta can aggregate into
beta-sheet oligomers and fibrils, which are both neurotoxic.
Therefore, one of the main therapeutic approaches to cure or
delay AD onset and progression is targeting Abeta aggregation.
In the present study, we show that a pool of human gamma
immunoglobulins (IgG) protected cortical neurons from the
challenge with Abeta oligomers, as assayed by MTT reduction,
caspase-3 activation and cytoskeleton integrity. In addition, we
report the inhibitory effect of IgG on Abeta aggregation, as
shown by Thioflavin T assay, size exclusion chromatography and
atomic force microscopy. Similar results were obtained with
Palivizumab, a human anti-sincitial virus antibody. In order to
dissect the important domains, we cleaved the pool of human IgG
with papain to obtain Fab and Fc fragments. Using these cleaved
fragments, we functionally identified Fab as the immunoglobulin
fragment inhibiting Abeta aggregation, a result that was further
confirmed by an in silico structural model. Interestingly,
bioinformatic tools show a highly conserved structure able to
bind amyloid in the Fab region. Overall, our data strongly
support the inhibitory effect of human IgG on Abeta aggregation
and its neuroprotective role.
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VALLS COMAMALA, Victòria, GUIVERNAU, Biuse, BONET, Jaume, PUIG, Marta, PERÁLVAREZ MARÍN, Alex, PALOMER, Ernest, FERNÀNDEZ BUSQUETS, Xavier, ALTAFAJ, Xavier, TAJES ORDUÑA, Marta, PUIG PIJOAN, Albert, VICENTE GARCÍA, Rubén, OLIVA MIGUEL, Baldomero, MUÑOZ, Francisco j.. The antigen-binding fragment of human gamma immunoglobulin
prevents amyloid beta-peptide folding into beta-sheet to form
oligomers. _Oncotarget_. 2017. Vol. 8, núm. 25, pàgs. 41154-41165. [consulta: 23 de gener de 2026]. ISSN: 1949-2553. [Disponible a: https://hdl.handle.net/2445/110867]