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Updated: Apr 4, 2026

A Guide to Production, Crystallization, and Structure Determination of Human IKK1/α
Published on: November 2, 2018
[Construction and identification of eukaryotic expression vectors of IKKα carrying Ser176/180 phosphorylation site
Yan He1, Qianqian Zheng1, Yaqin Zhu1
1Laboratory of Cell Pathobiology, Ministry of Education Key Laboratory of Medical Cell Biology, Department of Cell Biology, College of Basic Medical Science, China Medical University, Shenyang 110001, China.
Objective:
To construct eukaryotic expression vectors of the inhibitor of nuclear factor Kappa-B kinaseα (IKKα) containing Ser176/180 phosphorylation site mutants.
Methods:
Using PCR, we amplified two IKKα gene fragments, one containing Ser176/180 site mutants and non-sense mutation KpnI and the other with non-sense mutation KpnI. They were subjected to double enzyme digestion, HindIII/KpnI and KpnI/EcoRI, respectively, and then subcloned into pEGFP that had also digested with HindIII/EcoRI beforehand. The location of pEGFP-IKKα (kinase activity, KA)/(kinase death, KD) fusion protein in the eukaryocytes and their effects on P65 nuclear translocation were observed under a confocal microscope. The fusion protein expressions were detected by Western blotting.
Results:
Sequencing analysis verified the fidelity of all plasmid DNA constructs. PEGFP-IKKα KA was mainly located in nucleus and cytoplasm, and regulated P65 nuclear shuttling. In contrast, pEGFP-IKKα KD was mostly localized in cytoplasm, and did not initiate P65 nuclear translocation. Western blotting confirmed the expressions of the fusion proteins.
Conclusion:
The eukaryotic expression vectors pEGFP-IKKα KA/KD were successfully constructed and well expressed in the eukaryocytes. The fusion proteins were located in different parts of the cells and exerted different effects on P65 nuclear translocation.
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