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Synthetic Antibodies

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Cover of 'Synthetic Antibodies'

Table of Contents

  1. Altmetric Badge
    Book Overview
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    Chapter 1 Antibody Mimetics, Peptides, and Peptidomimetics
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    Chapter 2 Construction of a scFv Library with Synthetic, Non-combinatorial CDR Diversity
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    Chapter 3 Enzymatic Assembly for scFv Library Construction
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    Chapter 4 Directed Evolution of Protein Thermal Stability Using Yeast Surface Display
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    Chapter 5 Whole Cell Panning with Phage Display
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    Chapter 6 Generating Conformation and Complex-Specific Synthetic Antibodies
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    Chapter 7 High-Throughput IgG Conversion of Phage Displayed Fab Antibody Fragments by AmplYFast
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    Chapter 8 Utilization of Selenocysteine for Site-Specific Antibody Conjugation
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    Chapter 9 Solubility Characterization and Imaging of Intrabodies Using GFP-Fusions
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    Chapter 10 Antibody Validation by Immunoprecipitation Followed by Mass Spectrometry Analysis
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    Chapter 11 Novel HPLC-Based Screening Method to Assess Developability of Antibody-Like Molecules
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    Chapter 12 Glycosylation Profiling of α/β T Cell Receptor Constant Domains Expressed in Mammalian Cells
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    Chapter 13 A Proximity-Based Assay for Identification of Ligand and Membrane Protein Interaction in Living Cells
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    Chapter 14 A Biotin Ligase-Based Assay for the Quantification of the Cytosolic Delivery of Therapeutic Proteins
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    Chapter 15 Data-Driven Antibody Engineering Using Genedata Biologics™
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    Chapter 16 Selection of Aptamers Against Whole Living Cells: From Cell-SELEX to Identification of Biomarkers
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    Chapter 17 Rapid Selection of RNA Aptamers that Activate Fluorescence of Small Molecules
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    Chapter 18 An Enzyme-Linked Aptamer Sorbent Assay to Evaluate Aptamer Binding
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    Chapter 19 Incorporating Aptamers in the Multiple Analyte Profiling Assays (xMAP): Detection of C-Reactive Protein
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    Chapter 20 Transferring the Selectivity of a Natural Antibody into a Molecularly Imprinted Polymer
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    Chapter 21 Preparation of Molecularly Imprinted Microspheres by Precipitation Polymerization
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    Chapter 22 Generation of Janus Molecularly Imprinted Polymer Particles
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    Chapter 23 Surface Engineering of Nanoparticles to Create Synthetic Antibodies
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    Chapter 24 H5N1 Virus Plastic Antibody Based on Molecularly Imprinted Polymers
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    Chapter 25 Replacement of Antibodies in Pseudo-ELISAs: Molecularly Imprinted Nanoparticles for Vancomycin Detection
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    Chapter 26 Cell and Tissue Imaging with Molecularly Imprinted Polymers
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    Chapter 27 Erratum
Attention for Chapter 26: Cell and Tissue Imaging with Molecularly Imprinted Polymers
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Chapter title
Cell and Tissue Imaging with Molecularly Imprinted Polymers
Chapter number 26
Book title
Synthetic Antibodies
Published in
Methods in molecular biology, March 2017
DOI 10.1007/978-1-4939-6857-2_26
Pubmed ID
Book ISBNs
978-1-4939-6855-8, 978-1-4939-6857-2
Authors

Maria Panagiotopoulou, Stephanie Kunath, Karsten Haupt, Bernadette Tse Sum Bui

Editors

Thomas Tiller

Abstract

Advanced tools for cell imaging are of particular interest as they can detect, localize and quantify molecular targets like abnormal glycosylation sites that are biomarkers of cancer and infection. Targeting these biomarkers is often challenging due to a lack of receptor materials. Molecularly imprinted polymers (MIPs) are promising artificial receptors; they can be tailored to bind targets specifically, be labeled easily, and are physically and chemically stable. Herein, we demonstrate the application of MIPs as artificial antibodies for selective labeling and imaging of cellular targets, on the example of hyaluronan and sialylation moieties on fixated human skin cells and tissues. Thus, fluorescently labeled MIP nanoparticles templated with glucuronic acid (MIPGlcA) and N-acetylneuraminic acid (MIPNANA) are respectively applied. Two different fluorescent probes are used: (1) MIPGlcA particles, ~400 nm in size are labeled with the dye rhodamine that target the extracellular hyaluronan on cells and tissue specimens and (2) MIP-coated InP/ZnS quantum dots (QDs) of two different colors, ~125 nm in size that target the extracellular and intracellular hyaluronan and sialylation sites. Green and red emitting QDs are functionalized with MIPGlcA and MIPNANA respectively, enabling multiplexed cell imaging. This is a general approach that can also be adapted to other target molecules on and in cells.

Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 20 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 20 100%

Demographic breakdown

Readers by professional status Count As %
Student > Doctoral Student 3 15%
Student > Ph. D. Student 3 15%
Student > Bachelor 2 10%
Student > Master 2 10%
Researcher 2 10%
Other 3 15%
Unknown 5 25%
Readers by discipline Count As %
Chemistry 5 25%
Biochemistry, Genetics and Molecular Biology 4 20%
Medicine and Dentistry 4 20%
Pharmacology, Toxicology and Pharmaceutical Science 1 5%
Agricultural and Biological Sciences 1 5%
Other 0 0%
Unknown 5 25%