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Stabilized phospholipid membranes in chromatography: toward membrane protein-functionalized stationary phases
by
Gallagher, Elyssia S.
, Aspinwall, Craig A.
, Mansfield, Elisabeth
in
Affinity
/ affinity chromatography
/ Analysis
/ Analytical Chemistry
/ Animals
/ Biochemistry
/ Bisphenol A
/ Characterization and Evaluation of Materials
/ Chemical analysis
/ Chemistry
/ Chemistry and Materials Science
/ Chromatography
/ Chromatography, Affinity - instrumentation
/ Chromatography, Affinity - methods
/ Enzymes
/ Food Science
/ Glucose
/ Humans
/ Laboratory Medicine
/ Lipids
/ Mathematical analysis
/ Membrane proteins
/ Membrane Proteins - chemistry
/ Membranes
/ Monitoring/Environmental Analysis
/ Phases
/ Phospholipids
/ Phospholipids - chemistry
/ Proteins
/ Reproducibility
/ Separation
/ Separation techniques
/ Signal transduction
/ Trace elements
/ Trends
2014
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Stabilized phospholipid membranes in chromatography: toward membrane protein-functionalized stationary phases
by
Gallagher, Elyssia S.
, Aspinwall, Craig A.
, Mansfield, Elisabeth
in
Affinity
/ affinity chromatography
/ Analysis
/ Analytical Chemistry
/ Animals
/ Biochemistry
/ Bisphenol A
/ Characterization and Evaluation of Materials
/ Chemical analysis
/ Chemistry
/ Chemistry and Materials Science
/ Chromatography
/ Chromatography, Affinity - instrumentation
/ Chromatography, Affinity - methods
/ Enzymes
/ Food Science
/ Glucose
/ Humans
/ Laboratory Medicine
/ Lipids
/ Mathematical analysis
/ Membrane proteins
/ Membrane Proteins - chemistry
/ Membranes
/ Monitoring/Environmental Analysis
/ Phases
/ Phospholipids
/ Phospholipids - chemistry
/ Proteins
/ Reproducibility
/ Separation
/ Separation techniques
/ Signal transduction
/ Trace elements
/ Trends
2014
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Stabilized phospholipid membranes in chromatography: toward membrane protein-functionalized stationary phases
by
Gallagher, Elyssia S.
, Aspinwall, Craig A.
, Mansfield, Elisabeth
in
Affinity
/ affinity chromatography
/ Analysis
/ Analytical Chemistry
/ Animals
/ Biochemistry
/ Bisphenol A
/ Characterization and Evaluation of Materials
/ Chemical analysis
/ Chemistry
/ Chemistry and Materials Science
/ Chromatography
/ Chromatography, Affinity - instrumentation
/ Chromatography, Affinity - methods
/ Enzymes
/ Food Science
/ Glucose
/ Humans
/ Laboratory Medicine
/ Lipids
/ Mathematical analysis
/ Membrane proteins
/ Membrane Proteins - chemistry
/ Membranes
/ Monitoring/Environmental Analysis
/ Phases
/ Phospholipids
/ Phospholipids - chemistry
/ Proteins
/ Reproducibility
/ Separation
/ Separation techniques
/ Signal transduction
/ Trace elements
/ Trends
2014
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Stabilized phospholipid membranes in chromatography: toward membrane protein-functionalized stationary phases
Journal Article
Stabilized phospholipid membranes in chromatography: toward membrane protein-functionalized stationary phases
2014
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Overview
Transmembrane protein (TMP)-functionalized materials have resulted in powerful new methods in chemical analysis. Of particular interest is the development of high-throughput, TMP-functionalized stationary phases for affinity chromatography of complex mixtures of analytes. Several natural and synthetic phospholipids and lipid mimics have been used for TMP reconstitution, although the resulting membranes often lack the requisite chemical and temporal stability for long-term use, a problem that is exacerbated in flowing separation systems. Polymerizable lipids with markedly increased membrane stability and TMP functionality have been developed over the past two decades. More recently, these lipids have been incorporated into a range of analytical methods, including separation techniques, and are now poised to have a significant impact on TMP-based separations. Here, we describe current methods for preparing TMP-containing stationary phases and examine the potential utility of polymerizable lipids in TMP affinity chromatography.
Publisher
Springer Berlin Heidelberg,Springer,Springer Nature B.V
Subject
/ Analysis
/ Animals
/ Characterization and Evaluation of Materials
/ Chemistry and Materials Science
/ Chromatography, Affinity - instrumentation
/ Chromatography, Affinity - methods
/ Enzymes
/ Glucose
/ Humans
/ Lipids
/ Membrane Proteins - chemistry
/ Monitoring/Environmental Analysis
/ Phases
/ Proteins
/ Trends
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