一種光控神經退行性相關蛋白p62聚集的研究模型構建
首發時間:2023-06-27
摘要:目的:構建一種ALS/FTD(amyotrophic lateral sclerosis/frontotemporal dementia)相關蛋白p62的光控研究工具,在多種細胞模型中實現對p62相分離能力的人工控制。方法:利用同源重組技術,將p62頭端的PB1結構域替換為CRY2-mCherry。首先設計包含同源臂的引物,利用PCR線性化pCMV-CRY2-mCherry質粒模板并擴增p62 Δ1-122目的片段,在各自純化后進行同源重組反應并測序驗證pCMV-CRY2-mCherry-p62 Δ1-122(opto-p62)質粒的成功構建。隨后在HEK 293細胞和SH-SY5Y細胞中表達opto-p62,通過藍光刺激誘導其在細胞質內發生相分離,形成具備流動性的光控p62小體,并對opto-p62相變能力的影響因素和其他性質進行研究。結果:p62在細胞內形成的p62小體具備流動性。HEK 293細胞和SH-SY5Y細胞中過表達的opto-p62在波長488 nm的藍光刺激下可以發生相變,形成光控p62小體。opto-p62的相變能力與蛋白表達強度和藍光光照強度正相關,且光照形成的p62體可以招募p62相關蛋白。
關鍵詞: 神經退行性疾病 肌萎縮側索硬化 額顳葉癡呆 相分離
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Construction of a photo-controllable model for aggregationofneurodegenerative disease-associated protein p62
Abstract:Objective: To Construct a light control model of ALS/FTD (amyotrophic lateral sclerosis/frontotemporal dementia)-associated protein p62, and achieve manipulation of p62 phase transition in multiple cell lines. Methods: PB1 domain of p62 was replaced with CRY2-mCherry by homologous recombination. pCMV-CRY2-mCherry plasmid template were linearized and the p62 Δ1-122 sequence were amplified using PCR. Homologous recombination reactions were performed after purification and the product were sequenced to verify the successful of pCMV-CRY2-mCherry-p62 Δ1-122(opto-p62)construct. Opto-p62 was expressed in HEK 293 cells and SH-SY5Y cells, and were stimulated by blue light to form light-induced p62 bodies. The properties and factors affecting phase transition ability of opto-p62 were investigated.Results: The p62 bodies were liquid-like. Opto-p62 overexpressed in HEK 293 cells and SH-SY5Y cells can undergo phase transition to form light-induced p62 bodies under blue light stimulation at a wavelength of 488 nm. Opto-p62 phase transition ability was positively correlated with protein expression intensity and blue light intensity, and the light-induced p62 bodies can recruit p62-related proteins.
Keywords: Neurodegenerative disease Amyotrophic lateral sclerosis Frontotemporal Dementia LLPS
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一種光控神經退行性相關蛋白p62聚集的研究模型構建
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