The Structure and Dynamics of BmR1 Protein fromBrugia malayi: In Silico Approaches

International Journal of Molecular Sciences

Theam Soon Lim¹  Gee Jun Tye¹  Yee Siew Choong¹  Rahmah Noordin¹  Bee Yin Khor¹ 

[1] Institute for Research in Molecular Medicine, Universiti Sains Malaysia, Minden, Penang 11800, Malaysia;

关键词: Brugia malayi;    BmR1 protein;    protein structure prediction;    epitope prediction;    molecular dynamics simulation;   

DOI  :  10.3390/ijms150611082

来源: DOAJ

【 摘 要 】

Brugia malayi is a filarial nematode, which causes lymphatic filariasis in humans. In 1995, the disease has been identified by the World Health Organization (WHO) as one of the second leading causes of permanent and long-term disability and thus it is targeted for elimination by year 2020. Therefore, accurate filariasis diagnosis is important for management and elimination programs. A recombinant antigen (BmR1) from the Bm17DIII gene product was used for antibody-based filariasis diagnosis in “Brugia Rapid”. However, the structure and dynamics of BmR1 protein is yet to be elucidated. Here we study the three dimensional structure and dynamics of BmR1 protein using comparative modeling, threading and ab initio protein structure prediction. The best predicted structure obtained via an ab initio method (Rosetta) was further refined and minimized. A total of5 ns molecular dynamics simulation were performed to investigate the packing of the protein. Here we also identified three epitopes as potential antibody binding sites from the molecular dynamics average structure. The structure and epitopes obtained from this study can be used to design a binder specific against BmR1, thus aiding future development ofantigen-based filariasis diagnostics to complement the current diagnostics.

【 授权许可】

Unknown