细胞膜过氧物酶体导入受体 PEX5 的扩散和相互作用动力学。

IF 2.4 Q3 BIOPHYSICS Biophysical reports Pub Date : 2022-06-08 DOI:10.1016/j.bpr.2022.100055
S Galiani, K Reglinski, P Carravilla, A Barbotin, I Urbančič, J Ott, J Sehr, E Sezgin, F Schneider, D Waithe, P Hublitz, W Schliebs, R Erdmann, C Eggeling
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引用次数: 0

摘要

细胞功能有赖于过氧物酶体等细胞器的正常运作。这些细胞器依赖于从细胞质中导入蛋白质。过氧物酶体导入受体 PEX5 在细胞质中吸收目标蛋白质,并将其转运到过氧物酶体基质中。然而,到目前为止,它与细胞质的分子相互作用还没有被直接披露。在这里,我们将先进的光学显微镜和光谱技术(如荧光相关光谱和受激发射损耗显微镜)与生化工具相结合,详细描述了 PEX5 的胞浆扩散和相互作用动力学。除其他特征外,我们还强调了 PEX5 的缓慢扩散,这种扩散与聚集或目标结合无关,但通过其 N 端结构域与细胞膜相互作用伙伴相关联。这为研究受体在细胞质中的功能提供了新的视角,同时也凸显了利用互补显微镜工具,通过研究其扩散动力学来解密细胞质中分子相互作用的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Diffusion and interaction dynamics of the cytosolic peroxisomal import receptor PEX5.

Cellular functions rely on proper actions of organelles such as peroxisomes. These organelles rely on the import of proteins from the cytosol. The peroxisomal import receptor PEX5 takes up target proteins in the cytosol and transports them to the peroxisomal matrix. However, its cytosolic molecular interactions have so far not directly been disclosed. Here, we combined advanced optical microscopy and spectroscopy techniques such as fluorescence correlation spectroscopy and stimulated emission depletion microscopy with biochemical tools to present a detailed characterization of the cytosolic diffusion and interaction dynamics of PEX5. Among other features, we highlight a slow diffusion of PEX5, independent of aggregation or target binding, but associated with cytosolic interaction partners via its N-terminal domain. This sheds new light on the functionality of the receptor in the cytosol as well as highlighting the potential of using complementary microscopy tools to decipher molecular interactions in the cytosol by studying their diffusion dynamics.

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来源期刊
Biophysical reports
Biophysical reports Biophysics
CiteScore
2.40
自引率
0.00%
发文量
0
审稿时长
75 days
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