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Identification and characterization of antibodies elicited by human cystatin C fragment.

Authors :
Behrendt, Izabela
Prądzińska, Martyna
Spodzieja, Marta
Czaplewska, Paulina
Kołodziejczyk, Aleksandra S.
Szymańska, Aneta
Kasprzykowski, Franciszek
Lundström, Susanna L.
Zubarev, Roman A.
Rodziewicz‐Motowidło, Sylwia
Source :
Journal of Molecular Recognition; Apr2018, Vol. 31 Issue 4, p1-1, 13p
Publication Year :
2018

Abstract

Abstract: Amyloid formation is associated with a number of neurodegenerative diseases that affect the independence and quality of life of aging populations. One of rather atypical, occurring at a young age amyloidosis is hereditary cystatin C amyloid angiopathy (HCCAA) related to aggregation of L68Q variant of human cystatin C (hCC). Human cystatin C plays a very important role in many aspects of human health; however, its amyloidogenic properties manifested in HCCAA present a real, lethal threat to some populations and any work on factors that can affect possible influencing hCC aggregation is not to overestimate. It was proved that interaction of hCC with monoclonal antibodies suppresses significantly hCC dimerization process. Therefore, immunotherapy seems to be the right approach toward possible HCCAA treatment. In this work, the hCC fragment encompassing residue 60‐70 (in 2 variants: linear peptide and multiple antigenic peptide) was used as an immunogen in rabbit immunization. As a result, specific anti‐hCC antibodies were found in both rabbit sera. Surprisingly, rabbit antibodies were obtained after immunization with only a short peptide. The obtained antibodies were characterized, and their influence on the aggregation propensity of the hCC molecules was evaluated. The antibodies turned out not to have any significant influence on the cystatin C dimerization process. Nevertheless, we hope that antibodies elicited in rabbits by other hCC fragments could lead to elaboration of effective treatment against HCCAA. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
09523499
Volume :
31
Issue :
4
Database :
Complementary Index
Journal :
Journal of Molecular Recognition
Publication Type :
Academic Journal
Accession number :
128462743
Full Text :
https://doi.org/10.1002/jmr.2689