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Functionalized Nano-adsorbent for Affinity Separation of Proteins

Thiol-functionalized silica nanospheres (SiO(2)-SH NSs) with an average diameter of 460 nm were synthesized through a hydrothermal route. Subsequently, the prepared SiO(2)-SH NSs were modified by SnO(2) quantum dots to afford SnO(2)/SiO(2) composite NSs possessing obvious fluorescence, which could b...

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Detalles Bibliográficos
Autores principales: Zou, Xueyan, Yang, Fengbo, Sun, Xin, Qin, Mingming, Zhao, Yanbao, Zhang, Zhijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5976561/
https://www.ncbi.nlm.nih.gov/pubmed/29846826
http://dx.doi.org/10.1186/s11671-018-2531-4
Descripción
Sumario:Thiol-functionalized silica nanospheres (SiO(2)-SH NSs) with an average diameter of 460 nm were synthesized through a hydrothermal route. Subsequently, the prepared SiO(2)-SH NSs were modified by SnO(2) quantum dots to afford SnO(2)/SiO(2) composite NSs possessing obvious fluorescence, which could be used to trace the target protein. The SnO(2)/SiO(2) NSs were further modified by reduced glutathione (GSH) to obtain SnO(2)/SiO(2)-GSH NSs, which can specifically separate glutathione S-transferase-tagged (GST-tagged) protein. Moreover, the peroxidase activity of glutathione peroxidase 3 (GPX3) separated from SnO(2)/SiO(2)-GSH NSs in vitro was evaluated. Results show that the prepared SnO(2)/SiO(2)-GSH NSs exhibit negligible nonspecific adsorption, high concentration of protein binding (7.4 mg/g), and good reused properties. In the meantime, the GST-tagged GPX3 separated by these NSs can retain its redox state and peroxidase activity. Therefore, the prepared SnO(2)/SiO(2)-GSH NSs might find promising application in the rapid separation and purification of GST-tagged proteins.