Diffusion and interaction dynamics of the cytosolic peroxisomal import receptor PEX5

被引:4
作者
Galiani, S. [1 ,2 ]
Reglinski, K. [1 ,3 ,4 ,5 ]
Carravilla, P. [3 ,4 ,6 ,7 ]
Barbotin, A. [1 ,8 ]
Urbancic, I. [1 ,9 ]
Ott, J. [10 ]
Sehr, J. [10 ]
Sezgin, E. [1 ,11 ]
Schneider, F. [12 ]
Waithe, D. [2 ,13 ]
Hublitz, P. [15 ]
Schliebs, W. [10 ]
Erdmann, R. [10 ]
Eggeling, C. [1 ,2 ,3 ,4 ,14 ]
机构
[1] Univ Oxford, MRC Weatherall Inst Mol Med, MRC Human Immunol Unit, Oxford, England
[2] Univ Oxford, MRC Weatherall Inst Mol Med, Wolfson Imaging Ctr, Oxford, England
[3] Leibniz Inst Photon Technol eV, Jena, Germany
[4] Friedrich Schiller Univ Jena, Inst Appl Opt & Biophys, Jena, Germany
[5] Univ Hosp Jena, Jena, Germany
[6] Univ Basque Country UPV EHU, Dept Biochem & Mol Biol, Bilbao, Spain
[7] Univ Basque Country, Inst Bio Fis UPV EHU, CSIC, Leioa, Spain
[8] Univ Oxford, Dept Engn Sci, Oxford, England
[9] Jozef Stefan Inst, Condensed Matter Phys Dept, Lab Biophys, Ljubljana, Slovenia
[10] Ruhr Univ Bochum, Inst Biochem & Pathobiochem, Syst Biochem, Bochum, Germany
[11] Karolinska Inst, Dept Womens & Childrens Hlth, Sci Life Lab, Solna, Sweden
[12] Univ Oxford, Kennedy Inst Rheumatol, Oxford, England
[13] Univ Oxford, MRC Weatherall Inst Mol Med, WIMM Ctr Computat Biol, Oxford, England
[14] Jena Ctr Soft Matter JCSM, Jena, Germany
[15] Univ Oxford, MRC Weatherall Inst Mol Med, WIMM Genome Engn Serv, Oxford, England
来源
BIOPHYSICAL REPORTS | 2022年 / 2卷 / 02期
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
FLUORESCENCE CORRELATION SPECTROSCOPY; PLASMA-MEMBRANE; PROTEIN IMPORT; STED-FCS; BINDING; CELL; LOCALIZATION; RECOGNITION; MICROSCOPY; RECOVERY;
D O I
10.1016/j.bpr.2022.100055
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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 com-bined advanced optical microscopy and spectroscopy techniques such as fluorescence correlation spectroscopy and stimu-lated 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 func-tionality 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.
引用
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页数:15
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