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  • 1
    Online Resource
    Online Resource
    Waltham, Mass. [u.a.] : Elsevier, Academic Press
    UID:
    gbv_822041073
    Format: Online-Ressource (XXIV, 651 S.) , Ill., graph. Darst.
    Edition: Online-Ausg.
    ISBN: 9780128015216
    Series Statement: Methods in enzymology 556
    Content: Membrane Proteins - Production and Function Characterization a volume of Methods in Enzymology, encompasses chapters from the leading experts in the area of membrane protein biology. The chapters provide a brief overview of the topics covered and also outline step-by-step protocol. Illustrations and case example images are included wherever appropriate to help the readers understand the schematics and general experimental outlines.Volume of Methods In EnzymologyContains a collection of a diverse array of topics in the area of membrane protein biology ranging from recombinant expression, isolation, functional characterization, biophysical studies and crystallization
    Note: Description based upon print version of record , Front Cover; Membrane Proteins-Production and Functional Characterization; Copyright; Contents; Contributors; Preface; Section I: Recombinant Expression of Membrane Proteins; Chapter 1: Engineering Escherichia coli for Functional Expression of Membrane Proteins; 1. Introduction; 1.1. Green fluorescent protein as a folding reporter; 1.2. Antibiotic resistance marker protein for selection; 2. Preparation of Erythromycin-Sensitive E. coli Strain; 3. Preparation of Expression Plasmid; 3.1. Construction of expression vector for target protein-GFP-ErmC fusion; 3.2. Expression test , 3.2.1. Bacterial culture for protein expression and determination of whole-cell fluorescence3.2.2. Gel-based analysis of the expressed fusion constructs; 4. Selecting Cells for Better Expression; 5. Characterizing Evolved Strains; 5.1. Basic characterizations; 5.1.1. Plasmid copy number, DNA sequencing, and transcript levels; 5.2. Plasmid curing; 5.3. Functional assays; 6. Summary; Acknowledgments; References; Chapter 2: ACEMBLing a Multiprotein Transmembrane Complex: The Functional SecYEG-SecDF-YajC-YidC Holotranslocon Protein S...; 1. Introduction; 2. ACEMBLing the HTL Multiprotein Complex , 3. Purifying the HTL4. HTL Integrity and Activity; 4.1. Incorporation of translocation complexes in proteoliposomes; 4.2. Orientation of the reconstituted complexes; 4.3. Subunit interactions and activity of reconstituted translocation complexes; 4.3.1. ATP-stimulated protein secretion by SecA ATPase; 4.3.2. PMF-stimulated protein secretion activity; 4.3.3. Membrane protein insertion activity of the HTL; 5. Discussion and Conclusions; Acknowledgments; References; Chapter 3: Expression and Purification of OsVDAC4; 1. Introduction; 2. Equipment; 3. Materials; 3.1. Solutions and buffers , 4. Protocols4.1. Cloning; 4.2. Transformation protocol for protein expression; Duration: 2 h + overnight incubation; 4.3. Screening for colonies with high protein expression; Tips; 4.4. Expression and purification of OsVDAC4; 4.4.1. Soluble OsVDAC4 protein purification; Duration: 2-3 days; Tips; 4.4.2. OsVDAC4 purification from inclusion bodies; Duration: 2 days; Tips; 4.5. Tryptic digestion of OsVDAC4 for mass spectrometry; Duration: 2-3 days; 4.6. Functional characterization of OsVDAC4; 4.6.1. Liposome swelling assay; Duration: 2 days; Tips; Note; 4.6.2. Planar bilayer lipid membrane , Duration: 5-6hTips; Note; Acknowledgments; References; Chapter 4: Membrane Protein Expression in Lactococcus lactis; 1. Introduction; 2. Equipment and Materials; 3. Buffers and Media; 4. Protocol; 4.1. Preparation; 4.2. Duration; 4.3. Tip; 5. Step 1: Cloning the Target Gene into pNZ8048 and Transformation into L. lactis; 5.1. Overview; Amplification of the Target Gene by PCR; Restriction digestion; Preparation of pNZ vector; Restriction digestion; Ligation and pellet paint coprecipitation; Preparation of electrocompetent L. lactis; Transformation into electrocompetent L. lactis cells , 5.2. Tips
    Additional Edition: ISBN 9780128016251
    Additional Edition: Print version Membrane Proteins – Production and Functional Characterization
    Language: English
    Subjects: Biology
    RVK:
    RVK:
    Keywords: Membranproteine ; Electronic books ; Aufsatzsammlung
    Author information: Shukla, Arun K. 1981-
    Library Location Call Number Volume/Issue/Year Availability
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  • 2
    Online Resource
    Online Resource
    Amsterdam [u.a.] : Elsevier
    UID:
    b3kat_BV042488183
    Format: 1 Online-Ressource
    ISBN: 9780128015216 , 9780128016251
    Series Statement: Methods in enzymology 556
    Language: English
    Subjects: Biology
    RVK:
    RVK:
    Keywords: Membranproteine ; Aufsatzsammlung
    Author information: Shukla, Arun K. 1981-
    Library Location Call Number Volume/Issue/Year Availability
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  • 3
    Online Resource
    Online Resource
    Waltham, Massachusetts :Academic Press,
    UID:
    edoccha_9958132392402883
    Format: 1 online resource (693 p.)
    Edition: First edition.
    ISBN: 0-12-801521-7
    Series Statement: Methods in Enzymology ; Volume 556
    Note: Description based upon print version of record. , Front Cover; Membrane Proteins-Production and Functional Characterization; Copyright; Contents; Contributors; Preface; Section I: Recombinant Expression of Membrane Proteins; Chapter 1: Engineering Escherichia coli for Functional Expression of Membrane Proteins; 1. Introduction; 1.1. Green fluorescent protein as a folding reporter; 1.2. Antibiotic resistance marker protein for selection; 2. Preparation of Erythromycin-Sensitive E. coli Strain; 3. Preparation of Expression Plasmid; 3.1. Construction of expression vector for target protein-GFP-ErmC fusion; 3.2. Expression test , 3.2.1. Bacterial culture for protein expression and determination of whole-cell fluorescence3.2.2. Gel-based analysis of the expressed fusion constructs; 4. Selecting Cells for Better Expression; 5. Characterizing Evolved Strains; 5.1. Basic characterizations; 5.1.1. Plasmid copy number, DNA sequencing, and transcript levels; 5.2. Plasmid curing; 5.3. Functional assays; 6. Summary; Acknowledgments; References; Chapter 2: ACEMBLing a Multiprotein Transmembrane Complex: The Functional SecYEG-SecDF-YajC-YidC Holotranslocon Protein S...; 1. Introduction; 2. ACEMBLing the HTL Multiprotein Complex , 3. Purifying the HTL4. HTL Integrity and Activity; 4.1. Incorporation of translocation complexes in proteoliposomes; 4.2. Orientation of the reconstituted complexes; 4.3. Subunit interactions and activity of reconstituted translocation complexes; 4.3.1. ATP-stimulated protein secretion by SecA ATPase; 4.3.2. PMF-stimulated protein secretion activity; 4.3.3. Membrane protein insertion activity of the HTL; 5. Discussion and Conclusions; Acknowledgments; References; Chapter 3: Expression and Purification of OsVDAC4; 1. Introduction; 2. Equipment; 3. Materials; 3.1. Solutions and buffers , 4. Protocols4.1. Cloning; 4.2. Transformation protocol for protein expression; Duration: 2 h + overnight incubation; 4.3. Screening for colonies with high protein expression; Tips; 4.4. Expression and purification of OsVDAC4; 4.4.1. Soluble OsVDAC4 protein purification; Duration: 2-3 days; Tips; 4.4.2. OsVDAC4 purification from inclusion bodies; Duration: 2 days; Tips; 4.5. Tryptic digestion of OsVDAC4 for mass spectrometry; Duration: 2-3 days; 4.6. Functional characterization of OsVDAC4; 4.6.1. Liposome swelling assay; Duration: 2 days; Tips; Note; 4.6.2. Planar bilayer lipid membrane , Duration: 5-6hTips; Note; Acknowledgments; References; Chapter 4: Membrane Protein Expression in Lactococcus lactis; 1. Introduction; 2. Equipment and Materials; 3. Buffers and Media; 4. Protocol; 4.1. Preparation; 4.2. Duration; 4.3. Tip; 5. Step 1: Cloning the Target Gene into pNZ8048 and Transformation into L. lactis; 5.1. Overview; Amplification of the Target Gene by PCR; Restriction digestion; Preparation of pNZ vector; Restriction digestion; Ligation and pellet paint coprecipitation; Preparation of electrocompetent L. lactis; Transformation into electrocompetent L. lactis cells , 5.2. Tips , English
    Additional Edition: ISBN 0-12-801625-6
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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  • 4
    Online Resource
    Online Resource
    Waltham, Massachusetts :Academic Press,
    UID:
    almahu_9949697801002882
    Format: 1 online resource (693 p.)
    Edition: First edition.
    ISBN: 0-12-801521-7
    Series Statement: Methods in Enzymology ; Volume 556
    Note: Description based upon print version of record. , Front Cover; Membrane Proteins-Production and Functional Characterization; Copyright; Contents; Contributors; Preface; Section I: Recombinant Expression of Membrane Proteins; Chapter 1: Engineering Escherichia coli for Functional Expression of Membrane Proteins; 1. Introduction; 1.1. Green fluorescent protein as a folding reporter; 1.2. Antibiotic resistance marker protein for selection; 2. Preparation of Erythromycin-Sensitive E. coli Strain; 3. Preparation of Expression Plasmid; 3.1. Construction of expression vector for target protein-GFP-ErmC fusion; 3.2. Expression test , 3.2.1. Bacterial culture for protein expression and determination of whole-cell fluorescence3.2.2. Gel-based analysis of the expressed fusion constructs; 4. Selecting Cells for Better Expression; 5. Characterizing Evolved Strains; 5.1. Basic characterizations; 5.1.1. Plasmid copy number, DNA sequencing, and transcript levels; 5.2. Plasmid curing; 5.3. Functional assays; 6. Summary; Acknowledgments; References; Chapter 2: ACEMBLing a Multiprotein Transmembrane Complex: The Functional SecYEG-SecDF-YajC-YidC Holotranslocon Protein S...; 1. Introduction; 2. ACEMBLing the HTL Multiprotein Complex , 3. Purifying the HTL4. HTL Integrity and Activity; 4.1. Incorporation of translocation complexes in proteoliposomes; 4.2. Orientation of the reconstituted complexes; 4.3. Subunit interactions and activity of reconstituted translocation complexes; 4.3.1. ATP-stimulated protein secretion by SecA ATPase; 4.3.2. PMF-stimulated protein secretion activity; 4.3.3. Membrane protein insertion activity of the HTL; 5. Discussion and Conclusions; Acknowledgments; References; Chapter 3: Expression and Purification of OsVDAC4; 1. Introduction; 2. Equipment; 3. Materials; 3.1. Solutions and buffers , 4. Protocols4.1. Cloning; 4.2. Transformation protocol for protein expression; Duration: 2 h + overnight incubation; 4.3. Screening for colonies with high protein expression; Tips; 4.4. Expression and purification of OsVDAC4; 4.4.1. Soluble OsVDAC4 protein purification; Duration: 2-3 days; Tips; 4.4.2. OsVDAC4 purification from inclusion bodies; Duration: 2 days; Tips; 4.5. Tryptic digestion of OsVDAC4 for mass spectrometry; Duration: 2-3 days; 4.6. Functional characterization of OsVDAC4; 4.6.1. Liposome swelling assay; Duration: 2 days; Tips; Note; 4.6.2. Planar bilayer lipid membrane , Duration: 5-6hTips; Note; Acknowledgments; References; Chapter 4: Membrane Protein Expression in Lactococcus lactis; 1. Introduction; 2. Equipment and Materials; 3. Buffers and Media; 4. Protocol; 4.1. Preparation; 4.2. Duration; 4.3. Tip; 5. Step 1: Cloning the Target Gene into pNZ8048 and Transformation into L. lactis; 5.1. Overview; Amplification of the Target Gene by PCR; Restriction digestion; Preparation of pNZ vector; Restriction digestion; Ligation and pellet paint coprecipitation; Preparation of electrocompetent L. lactis; Transformation into electrocompetent L. lactis cells , 5.2. Tips , English
    Additional Edition: ISBN 0-12-801625-6
    Language: English
    Library Location Call Number Volume/Issue/Year Availability
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