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

Membrane protein crystallization.

Martin Caffrey1

  • 1Biochemistry, Biophysics, Chemistry, The Ohio State University, 100 West 18th Avenue, Columbus, OH 43210-1106, USA. caffrey.1@osu.edu <caffrey.1@osu.edu>

Journal of Structural Biology
|April 30, 2003
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

Structural and dynamic insights into agonist recognition and function of the thromboxane A<sub>2</sub> receptor.

Nature communications·2026
Same author

Structural basis of specific lysine transport by Pseudomonas aeruginosa permease LysP.

Nature communications·2025
Same author

Late-stage lipidation of peptides <i>via</i> aqueous thiol-michael addition to dehydroalanine (Dha).

Chemical communications (Cambridge, England)·2025
Same author

Solid-state NMR of membrane peptides and proteins in the lipid cubic phase.

Biophysical journal·2025
Same author

Computational Design of Cyclic Peptide Inhibitors of a Bacterial Membrane Lipoprotein Peptidase.

ACS chemical biology·2024
Same author

7.10 MAG. A Novel Host Monoacylglyceride for <i>In Meso</i> (Lipid Cubic Phase) Crystallization of Membrane Proteins.

Crystal growth & design·2024
Same journal

MLAC: MicroED-assisted ligand structure analysis in complexes and its application to hERG-ligand complexes.

Journal of structural biology·2026
Same journal

Ultrastructural evidence of autophagy-related processes and mitochondrial remodeling in the myxozoan parasite Henneguya piaractus.

Journal of structural biology·2026
Same journal

Architecture and dynamics of a supramolecular oxygen transport system in human homogentisate 1,2-Dioxygenase.

Journal of structural biology·2026
Same journal

Connecting pathways between mineralized fibrocartilage and bone at the Achilles tendon insertion.

Journal of structural biology·2026
Same journal

Structural and functional characterization of thermostable EstS1 esterase for BHET degradation.

Journal of structural biology·2026
Same journal

Following the white rabbit: multiscale 2D3D correlative imaging of bone structure.

Journal of structural biology·2026
See all related articles

New methods for membrane protein crystallization, including vesicle-fusion, bicelle, and in meso (cubic-phase) techniques, are advancing structural biology. These approaches leverage lipid self-assembly for improved crystal production, crucial for understanding protein function.

Area of Science:

  • Structural Biology
  • Biophysics
  • Crystallography

Background:

  • High-resolution membrane protein structures are essential for understanding biological function.
  • Crystallography is the primary method for obtaining such structures, but crystal production is a bottleneck.
  • Traditional surfactant-based methods have limitations for membrane protein crystallization.

Purpose of the Study:

  • To review and present current and emerging methods for membrane protein crystallization.
  • To focus on novel techniques that utilize lipid self-assembly properties.
  • To provide a primer on phase science relevant to these crystallization strategies.

Main Methods:

  • Overview of vesicle-fusion, bicelle, and in meso (cubic-phase) crystallization methods.

Related Experiment Videos

  • Detailed examination of the cubic-phase method, including practical aspects and challenges.
  • Review of bicelle and vesicle-fusion methods, with examples like bacteriorhodopsin crystallization.
  • Main Results:

    • The three novel methods exploit spontaneous self-assembly of lipids and detergents.
    • The cubic-phase method offers detailed strategies for optimizing crystallization of various membrane proteins.
    • Bicelle and vesicle-fusion methods have successfully crystallized bacteriorhodopsin, demonstrating potential applicability.

    Conclusions:

    • Novel lipid-based methods offer promising alternatives to traditional techniques for membrane protein crystallization.
    • Understanding phase science is critical for optimizing these crystallization strategies.
    • These advanced methods are crucial for overcoming current limitations in obtaining high-resolution membrane protein structures.