Kadam Ashlesha, Abuthakir Mohamed Hussain Syed, Jubin Tina, Vaishnav Jayvadan, Garg Abhishek, Balaji Chinthapalli, Suthar Devesh, Begum Rasheedunnisa
Department of Biochemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara- 390002, Gujarat, India.
Department of Bioinformatics, Bharathiar University, Coimbatore- 641046, Tamil Nadu, India.
Protein Expr Purif. 2021 Oct;186:105923. doi: 10.1016/j.pep.2021.105923. Epub 2021 May 29.
Poly (ADP-ribose) polymerase-1 (PARP-1) is a multifunctional protein that is associated with various biological processes like chromatin remodeling, DNA damage, cell death etc. In Dictyostelium discoideum, PARP-1 has also been implicated in cellular differentiation and development. However, its interacting proteins during multicellular development are not yet explored. Hence, the present study aims to identify PARP-1 interacting proteins during multicellular development of D. discoideum. BRCA1 C-terminus (BRCT) domain of PARP-1, which is mainly involved in protein-protein interactions was cloned in pGEX4T1 vector and developmental interactome of PARP-1 were analyzed by affinity purification-mass spectrometry. These interactions were further confirmed by in-silico protein-protein docking analysis, which led to identification of the proteins that show high affinity for BRCT domain. Initially, the protein structures were modeled on SWISS MODEL and PHYRE2 servers, refined by 3Drefine and validated by PROCHECK. Further, interaction sites of BRCT and the conserved regions in all interacting proteins were predicted using cons-PPISP and ConSurf, respectively. Finally, protein-protein docking analysis was done by HADDOCK. Our results identified 19 possible BRCT interacting proteins during D. discoideum development. Furthermore, interacting residues involved in the interactions and functional regions were explored. This is the first report where PARP-1's developmental interactome in D. discoideum is well established. The current findings demonstrate PARP-1's developmental interactome in D. discoideum and provide the groundwork to understand its regulated functions in developmental biology which would undoubtedly extend our perception towards developmental diseases in higher complex organisms and their treatment.
聚(ADP - 核糖)聚合酶 -1(PARP -1)是一种多功能蛋白质,与染色质重塑、DNA损伤、细胞死亡等多种生物学过程相关。在盘基网柄菌中,PARP -1也参与了细胞分化和发育过程。然而,其在多细胞发育过程中的相互作用蛋白尚未得到研究。因此,本研究旨在鉴定盘基网柄菌多细胞发育过程中与PARP -1相互作用的蛋白。PARP -1的BRCA1 C末端(BRCT)结构域主要参与蛋白质 - 蛋白质相互作用,将其克隆到pGEX4T1载体中,并通过亲和纯化 - 质谱分析PARP -1的发育相互作用组。这些相互作用通过计算机辅助蛋白质 - 蛋白质对接分析进一步得到证实,从而鉴定出对BRCT结构域具有高亲和力的蛋白质。最初,在SWISS MODEL和PHYRE2服务器上对蛋白质结构进行建模,通过3Drefine进行优化,并通过PROCHECK进行验证。此外,分别使用cons - PPISP和ConSurf预测BRCT的相互作用位点和所有相互作用蛋白中的保守区域。最后,通过HADDOCK进行蛋白质 - 蛋白质对接分析。我们的结果鉴定出盘基网柄菌发育过程中19种可能与BRCT相互作用的蛋白。此外,还探索了相互作用中涉及的相互作用残基和功能区域。这是首次全面确定盘基网柄菌中PARP -1的发育相互作用组的报告。目前的研究结果展示了盘基网柄菌中PARP -1的发育相互作用组,并为理解其在发育生物学中的调控功能奠定了基础,这无疑将扩展我们对高等复杂生物体发育疾病及其治疗的认识。