Abstract
Background: Tumor necrosis factor interacting protein (TRAIP/TRIP) is an important cell-signaling mole-cule that prevents the TNF-induced-nuclear factor kappa-light-chain-enhancer of activated B cells (NF-kappa B) activation via direct interaction with TRAF 2 protein. TRAIP is a crucial downstream signaling mole-cule, implicated in several signaling pathways. Due to these multifunctional effects, TRAIP is more related to cellular mitosis, chromosome segregation, and DNA damage response. Tumor necrosis factor interact-ing protein is a downstream signaling molecule that contains a RING domain with E3 ubiquitin ligase activity at the N terminal side followed by coiled-coil and C terminal leucine zipper domain. Human TRAIP is constituted of 469 amino acids with 76% sequence similarity with the mouse TRAIP protein. Although, the main inhibitory function of TRAIP has been known for decades, however, in vitro interaction of TRAIPCC domain with RAP80 Zinc finger motif has not been reported yet. Besides, RAP80, the binding partner of TRAIPCC protein has been implicated in DNA damage response.
Results: Our in vitro study shows that the TRAIP CC (64-166) associates with the RAP80 zinc finger of cor-responding amino acid 490-584. However, TRAIP CCLZ (66-260) and TRAIP RINGCC (1 = 157) failed to interact with the RAP80 zinc finger of corresponding amino acid 490-584. The current study reinforces TRAIP CC (64-166) and RAP80 zinc finger of corresponding amino acid 490-584 associates to forma com-plex. Moreover, SDS PAGE arbitrated the homogeneity of RAP80 Zinc finger and TRAIP CC of correspond-ing amino acid 490-584 and 64-166, respectively.
Conclusion: In vitro, a specific interaction was observed between the TRAIP CC (64-166) and the RAP80 zinc finger of the corresponding amino acid 490-584 and a specific binding area of the RAP80 zinc finger motif were investigated. The TRAIPCC region is required for the complex to bind to the RAP80-Zn finger motif. This strategy may be necessary for the RAP80 zinc finger activity to the TRAIP CC protein. (C) 2021 The Author(s). Published by Elsevier B.V. on behalf of King Saud University.