↓ Skip to main content

Antibody Engineering

Overview of attention for book
Cover of 'Antibody Engineering'

Table of Contents

  1. Altmetric Badge
    Book Overview
  2. Altmetric Badge
    Chapter 1 Antibody Design and Humanization via In Silico Modeling
  3. Altmetric Badge
    Chapter 2 Antibody Affinity Maturation by Computational Design
  4. Altmetric Badge
    Chapter 3 Use of IMGT® Databases and Tools for Antibody Engineering and Humanization
  5. Altmetric Badge
    Chapter 4 Construction of Human Naïve Antibody Gene Libraries
  6. Altmetric Badge
    Chapter 5 Construction of Synthetic Antibody Libraries
  7. Altmetric Badge
    Chapter 6 Construction of Histidine-Enriched Shark IgNAR Variable Domain Antibody Libraries for the Isolation of pH-Sensitive vNAR Fragments
  8. Altmetric Badge
    Chapter 7 Display Technologies for Generation of Ig Single Variable Domains
  9. Altmetric Badge
    Chapter 8 A Streamlined Approach for the Construction of Large Yeast Surface Display Fab Antibody Libraries
  10. Altmetric Badge
    Chapter 9 Phage Display and Selections on Purified Antigens
  11. Altmetric Badge
    Chapter 10 Selection of Antibodies to Transiently Expressed Membrane Proteins Using Phage Display
  12. Altmetric Badge
    Chapter 11 Selection of Antibody Fragments Against Structured DNA by Phage Display
  13. Altmetric Badge
    Chapter 12 Selection of Antibody Fragments by Yeast Display
  14. Altmetric Badge
    Chapter 13 Rapid Selection of High-Affinity Antibody scFv Fragments Using Ribosome Display
  15. Altmetric Badge
    Chapter 14 In Vitro Selection of Single-Domain Antibody (VHH) Using cDNA Display
  16. Altmetric Badge
    Chapter 15 Sequencing and Affinity Determination of Antigen-Specific B Lymphocytes from Peripheral Blood
  17. Altmetric Badge
    Chapter 16 Expression of IgG Monoclonals with Engineered Immune Effector Functions
  18. Altmetric Badge
    Chapter 17 An IRES-Mediated Tricistronic Vector for Efficient Generation of Stable, High-Level Monoclonal Antibody Producing CHO DG44 Cell Lines
  19. Altmetric Badge
    Chapter 18 Production, Purification, and Characterization of Antibody-TNF Superfamily Ligand Fusion Proteins
  20. Altmetric Badge
    Chapter 19 Chemoenzymatic Defucosylation of Therapeutic Antibodies for Enhanced Effector Functions Using Bacterial α-Fucosidases
  21. Altmetric Badge
    Chapter 20 Fc Glyco- and Fc Protein-Engineering: Design of Antibody Variants with Improved ADCC and CDC Activity
  22. Altmetric Badge
    Chapter 21 Fc Engineering: Tailored Synthetic Human IgG1-Fc Repertoire for High-Affinity Interaction with FcRn at pH 6.0
  23. Altmetric Badge
    Chapter 22 Measuring Antibody-Antigen Binding Kinetics Using Surface Plasmon Resonance
  24. Altmetric Badge
    Chapter 23 Parallel Evolution of Antibody Affinity and Thermal Stability for Optimal Biotherapeutic Development
  25. Altmetric Badge
    Chapter 24 The Use of Somatic Hypermutation for the Affinity Maturation of Therapeutic Antibodies
  26. Altmetric Badge
    Chapter 25 Selection and Use of Intracellular Antibodies
  27. Altmetric Badge
    Chapter 26 Site-Specific Radioactive Labeling of Nanobodies
Attention for Chapter 18: Production, Purification, and Characterization of Antibody-TNF Superfamily Ligand Fusion Proteins
Altmetric Badge

Citations

dimensions_citation
5 Dimensions

Readers on

mendeley
9 Mendeley
You are seeing a free-to-access but limited selection of the activity Altmetric has collected about this research output. Click here to find out more.
Chapter title
Production, Purification, and Characterization of Antibody-TNF Superfamily Ligand Fusion Proteins
Chapter number 18
Book title
Antibody Engineering
Published in
Methods in molecular biology, September 2018
DOI 10.1007/978-1-4939-8648-4_18
Pubmed ID
Book ISBNs
978-1-4939-8647-7, 978-1-4939-8648-4
Authors

Martin Siegemund, Nadine Beha, Dafne Müller, Siegemund, Martin, Beha, Nadine, Müller, Dafne

Abstract

Antibody-fusion proteins with ligands, e.g., of the TNF superfamily (TNFSF) can be adequately produced in mammalian expression systems. Here, we describe the transient production in adherent and suspension human embryonic kidney cells at laboratory scale, followed by purification procedures applying protein A and immobilized metal affinity chromatography for proteins with Fc domain and 6 × histidine-tag, respectively. In addition, characterization of the purified proteins by size exclusion chromatography is described.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 9 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 9 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 3 33%
Professor > Associate Professor 1 11%
Researcher 1 11%
Student > Bachelor 1 11%
Unknown 3 33%
Readers by discipline Count As %
Chemical Engineering 1 11%
Biochemistry, Genetics and Molecular Biology 1 11%
Nursing and Health Professions 1 11%
Agricultural and Biological Sciences 1 11%
Engineering 1 11%
Other 0 0%
Unknown 4 44%