Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Videos

A versatile method for deciphering plant membrane proteomes.

Norbert Rolland1, Myriam Ferro, Geneviève Ephritikhine

  • 1Laboratoire de Physiologie Cellulaire Végétale, UMR 5168 CEA/CNRS/INRA/Université Joseph Fourier, CEA-Grenoble, F-38054 Grenoble-cedex 9, France.

Journal of Experimental Botany
|April 6, 2006
PubMed
Summary
This summary is machine-generated.

Related Concept Videos

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

The fluorescence-activating and absorption-shifting tag (FAST), a versatile protein marker for live plant cell imaging.

The Plant journal : for cell and molecular biology·2026
Same author

Deciphering photosynthetic protein networks: a crosslinking-MS strategy for studying functional thylakoid membranes.

The Plant journal : for cell and molecular biology·2026
Same author

Integrative spectroscopic, geochemical, and microbiological approaches for assessing uranium (U) speciation and microbial diversity in a U-impacted wetland.

Ecotoxicology and environmental safety·2026
Same author

Design Differences and Usability Risks in GLP-1 Pen Injectors: A Comparative Study of a Generic and Reference Device.

PDA journal of pharmaceutical science and technology·2026
Same author

Targeting enhanced digestibility: Prioritizing low pith lignification to complement low p-coumaric acid content as environmental stress intensity increases.

PloS one·2025
Same author

Multi-Level Investigation in Arabidopsis of the Growth-Stimulating Effects of a Protein Hydrolysate Biostimulant.

Physiologia plantarum·2025
Same journal

Novel Imaging Approaches for Visualising Root-Mycorrhizal Fungal Interactions.

Journal of experimental botany·2026
Same journal

The ga3ox1b mutation reveals the crosstalk between gibberellin and other phytohormones in controlling the growth and development of female flowers in Cucurbita pepo.

Journal of experimental botany·2026
Same journal

Increased grain weight conferred by GW2 mutations in wheat does not translate into yield gains in multi-year field trials of near-isogenic lines.

Journal of experimental botany·2026
Same journal

Serendipita indica promotes rice phosphorus uptake by plasma membrane H+-ATPase OsA1-stimulated root hair growth.

Journal of experimental botany·2026
Same journal

The primary beta-galactosidase BGAL10 modulates pavement cell shape acquisition in Arabidopsis.

Journal of experimental botany·2026
Same journal

The link between phosphate starvation-triggered anthocyanin biosynthesis and jasmonate-driven regulation in tomato.

Journal of experimental botany·2026
See all related articles

This study presents a versatile proteomics strategy to identify proteins in plant membranes. The method, applied to spinach and Arabidopsis, enhances understanding of plant cell membrane functions.

Area of Science:

  • Plant molecular biology
  • Proteomics
  • Cellular and subcellular biology

Background:

  • Genomic data requires functional context from proteomic studies.
  • Understanding plant cell compartment functions necessitates detailed membrane proteome analysis.
  • Previous methods lacked comprehensive approaches for plant membrane protein identification.

Purpose of the Study:

  • To outline a versatile proteomics strategy for deciphering plant membrane proteomes.
  • To adapt and extend this strategy across various plant membrane types and species.
  • To validate the strategy's effectiveness in understanding plant membrane biochemistry.

Main Methods:

  • Preparation of highly purified membrane fractions from plant tissues.
  • Fractionation of membrane proteins using physico-chemical methods (e.g., solvent extraction, chemical washing).

Related Experiment Videos

  • Proteomic analysis involving 1D-gel electrophoresis, mass spectrometry, database searching, and subcellular localization validation.
  • Main Results:

    • The strategy was successfully applied to spinach chloroplast envelope membranes, thylakoids, and Arabidopsis membranes (chloroplast envelope, plasma, mitochondrial).
    • Protein fractionation simplified complex membrane proteomes for effective analysis.
    • Combined proteomics and bioinformatics approaches provided molecular-level insights into plant membrane machinery.

    Conclusions:

    • The developed proteomics strategy is effective for comprehensive plant membrane proteome analysis.
    • This approach links genomic information to functional understanding of plant cell compartments.
    • The findings advance the molecular-level comprehension of diverse plant membrane systems.