z-logo
open-access-imgOpen Access
Prionogenicity of vimentin surmised from the sequelog of anti-idiotypic antibodies toward the paratope of malignant-associated autologous anti-vimentin antibody, CLN-IgG (Pritumumab)
Author(s) -
Albert V. Hugwil,
Mark C. Glassy
Publication year - 2018
Publication title -
british journal of cancer research
Language(s) - English
Resource type - Journals
ISSN - 2631-5297
DOI - 10.31488/bjcr.1000104
Subject(s) - vimentin , antibody , paratope , chemistry , medicine , immunology , immunohistochemistry , monoclonal antibody
CLN-IgG (Pritumumab) is the natural human monoclonal antibody recognizing the altered-vimentin expressed on ectosomes of malignant cells. Comparative analysis of the sequelogous complementarity determining regions of the five anti-idiotypic antibodies to the paratope of CLN-IgG implied that the core epitope found in vimentin possessed prionogenic potential to form coacervates tending to amyloidosis, which are called vimentin prionogenic idiotope determining amino acids motif (vipidam). Sets of the sequelog of vipidam were found in countless prions and prion-like proteins. CLN-IgG carries over the sequelog of vipidam in its paratope, which was found not only in 14-3-3 proteins but also in α-synuclein. The effectiveness of Pritumumab on brain tumor regression was inferred by its intervention on vimentin prionogenesis via a prion silencing mechanism attributed to the chaperonic antibody like CLN-IgG (Pritumumab).

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom