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A Novel Apoptosis Correlated Molecule: Expression and Characterization of Protein Latcripin-1 from Lentinula edodes C(91–3)

An apoptosis correlated molecule—protein Latcripin-1 of Lentinula edodes C(91–3)—was expressed and characterized in Pichia pastoris GS115. The total RNA was obtained from Lentinula edodes C(91–3). According to the transcriptome, the full-length gene of Latcripin-1 was isolated with 3′-Full Rapid Amp...

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Detalles Bibliográficos
Autores principales: Liu, Ben, Zhong, Mintao, Lun, Yongzhi, Wang, Xiaoli, Sun, Wenchang, Li, Xingyun, Ning, Anhong, Cao, Jing, Zhang, Wei, Liu, Lei, Huang, Min
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Diversity Preservation International (MDPI) 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3382792/
https://www.ncbi.nlm.nih.gov/pubmed/22754362
http://dx.doi.org/10.3390/ijms13056246
Descripción
Sumario:An apoptosis correlated molecule—protein Latcripin-1 of Lentinula edodes C(91–3)—was expressed and characterized in Pichia pastoris GS115. The total RNA was obtained from Lentinula edodes C(91–3). According to the transcriptome, the full-length gene of Latcripin-1 was isolated with 3′-Full Rapid Amplification of cDNA Ends (RACE) and 5′-Full RACE methods. The full-length gene was inserted into the secretory expression vector pPIC9K. The protein Latcripin-1 was expressed in Pichia pastoris GS115 and analyzed by Sodium Dodecylsulfonate Polyacrylate Gel Electrophoresis (SDS-PAGE) and Western blot. The Western blot showed that the protein was expressed successfully. The biological function of protein Latcripin-1 on A549 cells was studied with flow cytometry and the 3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyl-tetrazolium Bromide (MTT) method. The toxic effect of protein Latcripin-1 was detected with the MTT method by co-culturing the characterized protein with chick embryo fibroblasts. The MTT assay results showed that there was a great difference between protein Latcripin-1 groups and the control group (p < 0.05). There was no toxic effect of the characterized protein on chick embryo fibroblasts. The flow cytometry showed that there was a significant difference between the protein groups of interest and the control group according to apoptosis function (p < 0.05). At the same time, cell ultrastructure observed by transmission electron microscopy supported the results of flow cytometry. The work demonstrates that protein Latcripin-1 can induce apoptosis of human lung cancer cells A549 and brings new insights into and advantages to finding anti-tumor proteins.