Probing the biophysical interaction between Neocarzinostatin toxin and EpCAM RNA aptamer
Data(s) |
08/01/2016
|
---|---|
Resumo |
Neocarzinostatin (NCS) a potent DNA-damaging, anti-tumor toxin extracted from Streptomyces carzinostaticus that recognizes double-stranded DNA bulge and induces DNA damage. 2 Fluoro (2F) Modified EpCAM RNA aptamer is a 23-mer that targets EpCAM protein, expressed on the surface of epithelial tumor cells. Understanding the interaction between NCS and the ligand is important for carrying out the targeted tumor therapy. In this study, we have investigated the biophysical interactions between NCS and 2-fluro Modified EpCAM RNA aptamer using Circular Dichroism (CD) and Infra-Red (IR) spectroscopy. The aromatic amino acid residues spanning the β sheets of NCS are found to participate in intermolecular interactions with 2 F Modified EpCAM RNA aptamer. In-silico modeling and simulation studies corroborate with CD spectra data. Furthermore, it reinforces the involvement of C and D1 strand of NCS in intermolecular interactions with EpCAM RNA aptamer. This the first report on interactions involved in the stabilization of NCS-EpCAM aptamer complex and will aid in the development of therapeutic modalities towards targeted cancer therapy. |
Identificador | |
Idioma(s) |
eng |
Publicador |
Elsevier |
Relação |
http://dro.deakin.edu.au/eserv/DU:30080643/athyala-probingthebiophysical-2016.pdf http://www.dx.doi.org/10.1016/j.bbrc.2015.11.109 |
Direitos |
2016, Elsevier |
Palavras-Chave | #CD spectroscopy #EpCAM aptamer #Insilico modeling #Neocarzinostatin #Antigens, Neoplasm #Aptamers, Nucleotide #Binding Sites #Cell Adhesion Molecules #Cytotoxins #Models, Chemical #Molecular Conformation #Molecular Docking Simulation #Protein Binding #Protein Interaction Mapping #Zinostatin #Science & Technology #Life Sciences & Biomedicine #Biochemistry & Molecular Biology #Biophysics #APO-NEOCARZINOSTATIN #GRAPHICS PROCESSORS #SECONDARY STRUCTURE #ANTITUMOR PROTEIN #CRYSTAL-STRUCTURE #CHROMOPHORE #APONEOCARZINOSTATIN #STABILIZATION #APOPROTEIN #ENEDIYNE |
Tipo |
Journal Article |