日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

A systematic bi-genomic split-GFP assay illuminates the mitochondrial matrix proteome and protein targeting routes

系统性的双基因组分裂GFP检测揭示了线粒体基质蛋白质组和蛋白质靶向途径

Bykov, Yury S; Zuttion, Solene; Edilbi, Dunya; Polozova, Marina; Arnold, Johanna; Malitsky, Sergey; Itkin, Maxim; Senger, Bruno; Klein, Ofir; Asraf, Yeynit; Meyer, Hadar; Becker, Hubert D; Kucharczyk, Roza; Schuldiner, Maya

Assigning mitochondrial localization of dual localized proteins using a yeast Bi-Genomic Mitochondrial-Split-GFP.

利用酵母双基因组线粒体分裂-GFP确定双重定位蛋白的线粒体定位

Bader Gaétan, Enkler Ludovic, Araiso Yuhei, Hemmerle Marine, Binko Krystyna, Baranowska Emilia, De Craene Johan-Owen, Ruer-Laventie Julie, Pieters Jean, Tribouillard-Tanvier Déborah, Senger Bruno, di Rago Jean-Paul, Friant Sylvie, Kucharczyk Roza, Becker Hubert Dominique

Crystal structure of Cex1p reveals the mechanism of tRNA trafficking between nucleus and cytoplasm

Cex1p的晶体结构揭示了tRNA在细胞核和细胞质之间运输的机制。

Nozawa, Kayo; Ishitani, Ryuichiro; Yoshihisa, Tohru; Sato, Mamoru; Arisaka, Fumio; Kanamaru, Shuji; Dohmae, Naoshi; Mangroo, Dev; Senger, Bruno; Becker, Hubert D; Nureki, Osamu

Yeast mitochondrial Gln-tRNA(Gln) is generated by a GatFAB-mediated transamidation pathway involving Arc1p-controlled subcellular sorting of cytosolic GluRS

酵母线粒体Gln-tRNA(Gln)是由GatFAB介导的转酰胺化途径产生的,该途径涉及Arc1p控制的胞质GluRS的亚细胞分选。

Frechin, Mathieu; Senger, Bruno; Brayé, Mélanie; Kern, Daniel; Martin, Robert Pierre; Becker, Hubert Dominique