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通过细胞表面工程重组体合成氧化钴纳米颗粒及其在抗癌治疗中的潜在应用

Cobalt Oxide Nanoparticle Synthesis by Cell-Surface-Engineered Recombinant and Potential Application for Anticancer Treatment.

作者信息

Kumaravel Ashokkumar, Sengupta Turbasu, Sathiyamoorthy Padmanaban, Jeong Jaehoon, Kang Sung Gu, Hong Soon Ho

机构信息

Department of Chemical Engineering, University of Ulsan, 93 Daehak-ro, Nam-gu, Ulsan 44610, Republic of Korea.

Department of Medical Nanotechnology, School of Chemical & Biotechnology, SASTRA Deemed University, Tamil Nadu 613401, India.

出版信息

ACS Omega. 2024 Jul 9;9(29):31373-31383. doi: 10.1021/acsomega.3c10246. eCollection 2024 Jul 23.

Abstract

Cell surface display engineering facilitated the development of a cobalt-binding hybrid . OmpC served as the molecular anchor for showcasing the cobalt-binding peptides (CBPs), creating the structural model of the hybrid OmpC-CBPs (OmpC-CP, OmpC-CF). Subsequently, the recombinant peptide's cobalt adsorption and retrieval effectiveness were evaluated at various concentrations. When subjected to a pH of 7 and a concentration of 2 mM, OmpC-CF exhibited a significantly higher cobalt recovery rate (2183.87 mol/g DCW) than OmpC-CP. The strain with bioadsorbed cobalt underwent thermal treatment at varying temperatures (400 °C, 500 °C, 600 °C, and 700 °C) and morphological characterization of the thermally decomposed cobalt nanoparticle oxides using diverse spectroscopy techniques. The analysis showed that nanoparticles confined themselves to metal ions, and EDS mapping detected the presence of cobalt on the cell surface. Finally, the nanoparticles' anticancer potential was assessed by subjecting them to heating at 500 °C in a furnace; they demonstrated noteworthy cytotoxicity, as evidenced by IC values of 59 μg/mL. These findings suggest that these nanoparticles hold promise as potential anticancer agents. Overall, this study successfully engineered a recombinant capable of efficiently binding to cobalt, producing nanoparticles with anticancer properties. The results of this investigation could have significant implications for advancing novel cancer therapies.

摘要

细胞表面展示工程促进了钴结合杂合体的开发。外膜蛋白C(OmpC)作为展示钴结合肽(CBP)的分子锚,构建了杂合体OmpC-CBP(OmpC-CP、OmpC-CF)的结构模型。随后,在不同浓度下评估了重组肽的钴吸附和回收效率。当pH值为7且浓度为2 mM时,OmpC-CF的钴回收率(2183.87 μmol/g干细胞重)显著高于OmpC-CP。对生物吸附钴的菌株在不同温度(400℃、500℃、600℃和700℃)下进行热处理,并使用多种光谱技术对热分解的钴纳米颗粒氧化物进行形态表征。分析表明,纳米颗粒局限于金属离子,能谱映射检测到细胞表面存在钴。最后,通过在炉中500℃加热对纳米颗粒的抗癌潜力进行评估;它们表现出显著的细胞毒性,IC值为59 μg/mL证明了这一点。这些发现表明,这些纳米颗粒有望成为潜在的抗癌药物。总体而言,本研究成功构建了一种能够有效结合钴的重组体,产生具有抗癌特性的纳米颗粒。本研究结果可能对推进新型癌症治疗具有重要意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4613/11270722/3cc7b90cf4f0/ao3c10246_0001.jpg

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