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A magnetic calcium phosphate for selective capture of multi-phosphopeptides.
Ren, FangKun; Dai, JunYong; Zhang, JingYi; Luan, YanFei; Yang, Fan; Shen, Jian; Liu, HaiLong; Zhou, JiaHong.
Affiliation
  • Ren F; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Dai J; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Zhang J; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Luan Y; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Yang F; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Shen J; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China.
  • Liu H; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China. Electronic address: lhl7083609@163.com.
  • Zhou J; College of Life Sciences, Jiangsu Key Laboratory Biofunctional Materials, Nanjing Normal University, Nanjing 210023, China. Electronic address: zhoujiahong@njnu.edu.cn.
Article in En | MEDLINE | ID: mdl-38603891
ABSTRACT
The specific enrichment of multi-phosphopeptides in the presence of non-phosphopeptides and mono-phosphopeptides was still a challenge for phosphoproteomics research. Most of these enrichment materials relied on Zn, Ti, Sn, and other rare precious metals as the bonding center to enrich multi-phosphopeptides while ignoring the use of common metal elements. The addition of rare metals increased the cost of the experiment, which was not conducive to their large-scale application in biomedical proteomics laboratories. In addition, multiple high-speed centrifugation steps also resulted in the loss of low-abundance multi-phosphopeptides in the treatment procedure of biological samples. This study proposed the use of calcium, a common element, as the central bonding agent for synthesizing magnetic calcium phosphate materials (designated as CaP-Fe3O4). These materials aim to capture multi-phosphopeptides and identifying phosphorylation sites. The current results demonstrate that CaP-Fe3O4 exhibited excellent selection specificity, high sensitivity, and stability in the enrichment of multi-phosphopeptides and the identification of phosphorylation sites. Additionally, the introduction of magnetic separation not only reduced the time required for multi-phosphopeptides enrichment but also prevented the loss of these peptides during high-speed centrifugation. These findings contribute to the widespread application and advancement of phosphoproteomics research.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphopeptides / Calcium Phosphates Limits: Humans Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci / J. chromatogr. B / Journal of chromatography. B (Print) Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: China Country of publication: Países Bajos

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Phosphopeptides / Calcium Phosphates Limits: Humans Language: En Journal: J Chromatogr B Analyt Technol Biomed Life Sci / J. chromatogr. B / Journal of chromatography. B (Print) Journal subject: ENGENHARIA BIOMEDICA Year: 2024 Document type: Article Affiliation country: China Country of publication: Países Bajos