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Heterologous Expression of Membrane Proteins: Methods and Protocols Third Edition 2022 [Pehme köide]

  • Formaat: Paperback / softback, 467 pages, kõrgus x laius: 254x178 mm, kaal: 920 g, 78 Illustrations, color; 16 Illustrations, black and white, 1 Paperback / softback
  • Sari: Methods in Molecular Biology 2507
  • Ilmumisaeg: 02-Jul-2023
  • Kirjastus: Humana
  • ISBN-10: 1071623702
  • ISBN-13: 9781071623701
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  • Formaat: Paperback / softback, 467 pages, kõrgus x laius: 254x178 mm, kaal: 920 g, 78 Illustrations, color; 16 Illustrations, black and white, 1 Paperback / softback
  • Sari: Methods in Molecular Biology 2507
  • Ilmumisaeg: 02-Jul-2023
  • Kirjastus: Humana
  • ISBN-10: 1071623702
  • ISBN-13: 9781071623701
Teised raamatud teemal:
This detailed volume explores protocols for the production of membrane proteins in a panel of heterologous organisms for structural studies. Beginning with techniques using E. coli as a host for the overproduction and purification of membrane proteins, the book continues with chapters covering mammalian membrane protein production in yeast, insect cells, mammalian cells, as well as using virus like particles and acellular systems. Additionally, new detergents and alternatives to detergents allowing membrane protein purification for structural analyses are described. The book closes with a chapter exploring the use of microscale thermophoresis (MST) to evaluate the binding activity of heterologously expressed proteins directly in crude membrane extracts. Written for the highly successful Methods in Molecular Biology series, chapters include introductions to their respective topics, lists of the necessary materials and reagents, step-by-step, readily reproducible laboratory protocols, and tips on troubleshooting and avoiding known pitfalls. 

Authoritative and up-to-date, Heterologous Expression of Membrane Proteins: Methods and Protocols, Third Edition serves as an ideal guide for scientists aiming to produce and purify functional recombinant membrane proteins for structural studies.
Solubilization and Purification of a5b1 Integrin from Rat Liver for
Reconstitution into Nanodiscs.- Membrane Proteins Production in Escherichia
coli: Protocols and Rules.- Functional Overexpression of Membrane Proteins in
E. coli: The Good, the Bad, and the Ugly.- Heterologous Expression of
Membrane Proteins in E. coli.- Overexpression of the ABC Transporter BmrA
within Intracellular Caveolæ in Escherichia coli.- Production of Membrane
Proteins in Pseudomonas stutzeri.- Overproduction of Membrane-Associated, and
Integrated, Proteins Using Saccharomyces cerevisiae.- Purification of
Membrane Proteins Overexpressed in Saccharomyces cerevisiae.- Production and
Purification of a GFP-Tagged ABC Transporter CaCdr1p.- Membrane Protein
Production in the Yeast, P. pastoris.- Production and Preparation of
Isotopically-Labelled Human Membrane Proteins in Pichia pastoris for
Fast-MAS-NMR Analyses.- Membrane Protein Production in Insect Cells.-
Thromboxane A2 G Protein-Coupled Receptor Production and Crystallization for
Structure Studies.- Production of Human ABC Transporters and
Oligosaccharyltransferase Complexes for Structural Studies.- The Heterologous
Expression and Purification of GPCRs.- Expression and Purification of the
Human Thyroid-Stimulating Hormone Receptor.- Optimization of Recombinant GPCR
Proteins for Biophysical and Structural Studies Using Virus-Like Particles.-
Peptide Tags and Domains for Expression and Detection of Mammalian Membrane
Proteins at the Cell Surface.- Tailor the Purification and Analysis of
Membrane Proteins with Modular Detergents.- Detergent Alternatives: Membrane
Protein Purification Using Synthetic Nanodisc Polymers.- Detergent-Free
Membrane Protein Purification Using SMA Polymer.- Cell-Free Expression of
GPCRs into Nanomembranes for Functional and Structural Studies.- Cell-Free
Expression of Proton-Coupled Folate Transporter in the Presence of
Nanodiscs.- Microscale Thermophoresis to Evaluate the Functionality of
Heterologously Overexpressed Membrane Proteins in Membrane Preparations.