Detergent Lipid Ratio

Detergent lipid ratio is the relative amount of detergent to membrane lipid in a biological membrane preparation, a parameter that controls how effectively membranes are disrupted and their components maintained in solution. Detergent molecules insert into lipid bilayers, forming mixed detergent-lipid micelles or related aggregates once their concentration and proportion exceed conditions needed for solubilization; changing the ratio can shift the balance between intact vesicles, partially solubilized membranes, and fully dispersed complexes. In biology, controlling this ratio supports membrane-protein extraction, purification, structural analysis, and reconstitution into artificial membranes. Optimizing it helps preserve protein folding and activity while producing reproducible experimental samples.

Detergent Lipid Ratio - Related Videos

Research

JoVE EoE - Bacterial Growth and Techniques

Enrichment of Bacterial Lipoproteins Using Non-Ionic Detergent Phase Separation

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2025

Source: Armbruster, K. M., Meredith, T. C. Enrichment of Bacterial Lipoproteins and Preparation of N-terminal Lipopeptides for Structural Determination by Mass Spectrometry. J. Vis. Exp. (2018)This video demonstrates the enrichment of bacterial lipoproteins using a non-ionic detergent that undergoes phase separation upon warming. Through sequential temperature shifts and centrifugation steps, lipoproteins are selectively partitioned into the detergent phase, while non-lipoprotein contaminants...

Detergent-assisted Reconstitution of Recombinant Drosophila Atlastin into Liposomes for Lipid-mixing Assays

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Cited by 2 •

2019

Biological membrane fusion is catalyzed by specialized fusion proteins. Measuring the fusogenic properties of proteins can be achieved by lipid mixing assays. We present a method for purifying recombinant Drosophila atlastin, a protein that mediates homotypic fusion of the ER, reconstituting it to preformed liposomes, and testing for fusion capacity.

Research

JoVE Journal - Biochemistry
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Detergent-free Ultrafast Reconstitution of Membrane Proteins into Lipid Bilayers Using Fusogenic Complementary-charged Proteoliposomes.

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Cited by 6 •

2018

Here we present two ultrafast protocols for reconstitution of membrane proteins into fusogenic proteoliposomes, and fusion of such proteoliposomes with target lipid bilayers for detergent-free delivery of these membrane proteins into the postfusion bilayer. The combination of these approaches enables fast and easily controlled assembly of complex multi-component membrane systems.

Research

JoVE Journal - Biology
Free Sample

Crystallization of Membrane Proteins in Lipidic Mesophases

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Cited by 30 •

2011

The protocols describe the essential steps for obtaining diffraction quality crystals of a membrane protein starting from reconstitution of the protein in a lipidic cubic phase (LCP), finding initial conditions with LCP-FRAP pre-crystallization assays, setting up LCP crystallization trials and harvesting crystals.

High-throughput Crystallization of Membrane Proteins Using the Lipidic Bicelle Method

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Cited by 27 •

2012

Bicelles are lipid/amphiphile mixtures that maintain membrane proteins (MPs) within a lipid bilayer but have unique phase behavior that facilitates high-throughput screening by crystallization robots. This technique has successfully produced a number of high-resolution structures from both prokaryotic and eukaryotic sources. This video describes protocols for generating the lipidic bicelle mixture, incorporating MPs into the bicelle mixture, setting up crystallizations trials (manually as well...

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