Quantitative analysis of peroxisomal protein import in vitro

Experimental Cell Research

Volumn 263, Issue 1, 2001, Pages 98-106

  Terlecky, S R ^a   Legakis, J E ^a   Hueni, S E ^a   Subramani, S ^b  

^a WAYNE STATE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^b UNIVERSITY OF CALIFORNIA   (United States)

Author keywords

Membrane; Organelle; Peroxisome matrix; Protein targeting; Zinc

Indexed keywords

ADENOSINE TRIPHOSPHATE; ANTIBODY; LUCIFERASE; MEMBRANE PROTEIN; PROTEIN PEX2P; PROTEIN PEX5P; PROTEIN PMP70; RECEPTOR; UNCLASSIFIED DRUG; ZINC; ZINC FINGER PROTEIN;

ANIMAL CELL; ARTICLE; BIOTINYLATION; CELL FRACTIONATION; CELL ORGANELLE; CONFOCAL LASER MICROSCOPY; ENZYME LINKED IMMUNOSORBENT ASSAY; FIBROBLAST; FLUORESCENCE; HUMAN; HUMAN CELL; IN VITRO STUDY; MEMBRANE DAMAGE; NONHUMAN; PEROXISOME; PRIORITY JOURNAL; PROTEIN LOCALIZATION; PROTEIN TARGETING; PROTEIN TRANSPORT; QUANTITATIVE ASSAY; TEMPERATURE DEPENDENCE; TIME; ZELLWEGER SYNDROME;

EID: 0035242491     PISSN: 00144827     EISSN: None     Source Type: Journal    
DOI: 10.1006/excr.2000.5111     Document Type: Article

References (33)

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5. The effects of chaperones and the influence of protein assembly on peroxisomal protein import
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7. A conserved tripeptide sorts proteins to peroxisomes
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9. Multiple PEX genes are required for proper subcellular distribution and stability of Pex5, the PTS1 receptor: Evidence that PTS1 protein import is mediated by a cycling receptor
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15. Components involved in peroxisome import, biogenesis, proliferation, turnover, and movement
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