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Interfacial modification of recombinant protein for immunoglobulin G adsorption with spindle-shaped MOF as nano molecular containers.
Wang, Kai; Zhang, Hongjin; Jin, Nishan; Zhou, Yutian; Guo, Xinli; Zhong, Wenbin; Li, Xin; Li, Xuwen; Zhang, Yang.
Afiliación
  • Wang K; Shenyang Key Laboratory of Medical Molecular Theranostic Probes in School of Pharmacy, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Zhang H; School of Basic Medicine, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Jin N; Shenyang Key Laboratory of Medical Molecular Theranostic Probes in School of Pharmacy, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Zhou Y; School of Basic Medicine, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Guo X; School of Basic Medicine, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Zhong W; School of Basic Medicine, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Li X; Department of Science and Technology, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China.
  • Li X; Department of Analytical Chemistry, College of Chemistry, Jilin University, Changchun, 130012, China. Electronic address: lixw@jlu.edu.cn.
  • Zhang Y; Shenyang Key Laboratory of Medical Molecular Theranostic Probes in School of Pharmacy, Shenyang Medical College, 146 Huanghe North Avenue, Shenyang, 110034, China. Electronic address: zhangyangpro@symc.edu.cn.
Talanta ; 280: 126535, 2024 Jul 09.
Article en En | MEDLINE | ID: mdl-39121618
ABSTRACT
Development of fresh solid phase extractant is critical for selective separation and purification of special proteins. Herein, we demonstrated a recombinant Staphylococcal Protein G (rSPG) with a His-tag modified the novel single-metal organic framework (rSPG@Ni-MOF-74). The proposed solid-phase extraction material possessed a uniform spindle-shaped structure, large surface area (709.60 m2 g-1) and pore volume (0.08 m3 g-1), high metal content (22.57 wt%), which facilitated the interaction between host and guest. As results, the composite displayed outstanding selective recognition and adsorption of IgG, due to synergistic effect of the binding ability of rSPG with the Fc region of IgG, maintained through hydrogen bonding and electrostatic attraction, as well as hydrophobic interaction. The adsorption performance and mechanism of rSPG@Ni-MOF-74 have been fully investigated. Additionally, the rSPG@Ni-MOF-74 composite could effectively separate IgG from serum obtained from healthy humans, with the purity of the separated IgG verified through SDS-PAGE analysis. Furthermore, LC-MS/MS analysis identified a high content of IgG (55.3 %) in the eluate from rSPG@Ni-MOF-74, suggesting the great potential of rSPG@Ni-MOF-74 in IgG separation and enrichment from complex matrix.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Talanta Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Talanta Año: 2024 Tipo del documento: Article País de afiliación: China