Abstract
HMGB1, composed of the A box, B box, and C tail domains, is a critical proinflammatory cytokine involved in diverse inflammatory diseases. The B box mediates proinflammatory activity, while the A box alone acts as a specific antagonist of HMGB1. The C tail contributes to the spatial structure of A box and regulates HMGB1 DNA binding specificity. It is unknown whether the C tail can enhance the anti-inflammatory effect of A box. In this study, we generated fusion proteins consisting of the A box and C tail, in which the B box was deleted and the A box and C tail were linked either directly or by the flexible linker sequence (Gly4Ser)3. In vitro and in vivo experiments showed that the two fusion proteins had a higher anti-inflammatory activity compared to the A box alone. This suggests that the fused C tail enhances the anti-inflammatory effect of the A box. © 2010 Wei Gong et al.
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CITATION STYLE
He, F., Gong, W., Zheng, Y., Chao, F., Li, Y., Xu, Z., … Li, S. (2010). The anti-inflammatory activity of HMGB1 A box is enhanced when fused with C-terminal acidic tail. Journal of Biomedicine and Biotechnology, 2010. https://doi.org/10.1155/2010/915234
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