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Study on the interaction protein of transcription factor Smad3 based on TurboID proximity labeling technology.
Yan, Biao; Zeng, Ting; Liu, Xiaoshan; Guo, Yuanyuan; Chen, Hongguang; Guo, Shuang; Liu, Wu.
Affiliation
  • Yan B; School of Basic Medical Sciences, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China.
  • Zeng T; Medicine Research Institute, Hubei Key Laboratory of Diabetes and Angiopathy, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China.
  • Liu X; School of Basic Medical Sciences, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China; School of Pharmacy, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China.
  • Guo Y; School of Basic Medical Sciences, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China.
  • Chen H; Medicine Research Institute, Hubei Key Laboratory of Diabetes and Angiopathy, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China. Electronic address: 94479558@qq.com.
  • Guo S; Medicine Research Institute, Hubei Key Laboratory of Diabetes and Angiopathy, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China. Electronic address: guoshuang@hbust.edu.cn.
  • Liu W; School of Basic Medical Sciences, Xianning Medical College, Hubei University of Science and Technology, Xianning 437000, Hubei, China. Electronic address: lw463684057@163.com.
Genomics ; 116(3): 110839, 2024 05.
Article in En | MEDLINE | ID: mdl-38537808
ABSTRACT
TurboID is a highly efficient biotin-labelling enzyme, which can be used to explore a number of new intercalating proteins due to the very transient binding and catalytic functions of many proteins. TGF-ß/Smad3 signaling pathway is involved in many diseases, especially in diabetic nephropathy and inflammation. In this paper, a stably cell line transfected with Smad3 were constructed by using lentiviral infection. To further investigate the function of TGF-ß/Smad3, the protein labeling experiment was conducted to find the interacting protein with Smad3 gene. Label-free mass spectrometry analysis was performed to obtain 491 interacting proteins, and the interacting protein hnRNPM was selected for IP and immunofluorescence verification, and it was verified that the Smad3 gene had a certain promoting effect on the expression of hnRNPM gene, and then had an inhibitory effect on IL-6. It lays a foundation for further study of the function of Smad3 gene and its involved regulatory network.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Smad3 Protein Limits: Humans Language: En Journal: Genomics Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Smad3 Protein Limits: Humans Language: En Journal: Genomics Year: 2024 Document type: Article