Chemical ligation : tools for biomolecule synthesis and modification /

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Bibliographic Details
Other Authors: D'Andrea, Luca D. (Editor), Romanelli, Alessandra (Editor)
Format: Electronic eBook
Language:English
Published: Hoboken, NJ : John Wiley & Sons, Inc., 2017.
Subjects:
Online Access:CONNECT

MARC

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245 0 0 |a Chemical ligation :  |b tools for biomolecule synthesis and modification /  |c edited by Luca D. D'Andrea, Alessandra Romanelli. 
264 1 |a Hoboken, NJ :  |b John Wiley & Sons, Inc.,  |c 2017. 
300 |a 1 online resource 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
500 |a Wiley EBA  |5 TMurS 
504 |a Includes bibliographical references and index. 
588 0 |a Print version record and CIP data provided by publisher. 
505 0 |6 880-01  |a Cover; Title Page; Copyright; Contents; List of Figures; List of Plates; List of Contributors; Preface; Chapter 1 Introduction to Chemical Ligation Reactions; 1.1 Introduction; 1.1.1 Chemical Synthesis of Proteins: From the Stepwise Synthesis to the Chemical Ligation Approach; 1.1.2 Chemical Modification of Proteins: From Conventional Methods to Chemoselective Labeling by Chemical Ligation; 1.2 Chemical Ligation Chemistries; 1.3 Imine Ligations; 1.3.1 Oxime Ligation; 1.3.2 Hydrazone Ligation; 1.3.3 Pictet-Spengler Ligation; 1.3.4 Thiazolidine Ligation; 1.4 Serine/Threonine Ligation (STL). 
505 8 |a 2.3.2 SEAon/off Concept and the Design of a One-Pot Three Peptide Segment Assembly Process2.3.3 SEA on/off Concept and the Solid-Phase Synthesis of Proteins in the N-to-C Direction; 2.4 Chemical Synthesis of HGF/SF Subdomains for Deciphering the Functioning of HGF/SF-MET System; 2.5 Conclusion; References; Chapter 3 Development of Serine/Threonine Ligation and Its Applications; 3.1 Introduction; 3.1.1 Protein Synthesis by SPPS; 3.1.2 Native Chemical Ligation (and Extended Desulfurization); 3.1.3 KAHA Ligation; 3.2 Serine/Threonine Ligation (STL); 3.2.1 SAL Ester Preparation. 
505 8 |a 3.2.2 N-Terminal-Protecting Group for Successive C-to-N Ser/Thr Ligations3.2.3 Scope and Limitations; 3.3 Application of STL in Protein Synthesis; 3.3.1 Consecutive STL of Peptides/Proteins; 3.3.2 STL-Mediated Peptide Cyclization; 3.3.3 Thiol SAL Ester-Mediated Aminolysis in Peptide Cyclization; 3.3.4 A Fluorogenic Probe for Recognizing 5-OH-Lys Inspired by STL; 3.3.5 Expressed Protein Semisynthesis via Ser/Thr Ligation; 3.4 Conclusion and Outlook; References; Chapter 4 Synthesis of Proteins by Native Chemical Ligation-Desulfurization Strategies; 4.1 Introduction. 
505 8 |a 4.2 Ligation-Desulfurization and Early Applications4.2.1 Metal-Free Desulfurization; 4.2.2 Ligation-Desulfurization toward the Synthesis of Proteins; 4.3 Beyond Native Chemical Ligation at Cysteine -- The Development of Thiolated Amino Acids and Their Application in Protein Synthesis; 4.3.1 Phenylalanine; 4.3.2 Valine; 4.3.3 Lysine; 4.3.4 Threonine; 4.3.5 Leucine; 4.3.6 Proline; 4.3.7 Glutamine; 4.3.8 Arginine; 4.3.9 Aspartic Acid; 4.3.10 Glutamic Acid; 4.3.11 Tryptophan; 4.3.12 GlcNAc-Asparagine; 4.3.13 Asparagine; 4.4 Ligation-Deselenization in the Chemical Synthesis of Proteins. 
650 0 |a Biosynthesis. 
650 0 |a Peptides  |x Synthesis. 
650 0 |a Proteins  |x Synthesis. 
650 0 |a Bioorganic chemistry. 
650 0 |a Chemistry, Organic. 
700 1 |a D'Andrea, Luca D.,  |e editor. 
700 1 |a Romanelli, Alessandra,  |e editor. 
730 0 |a WILEYEBA 
776 0 8 |i Print version:  |t Chemical ligation.  |d Hoboken, NJ : John Wiley & Sons, Inc., 2017  |z 9781119044109  |w (DLC) 2016052028 
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880 8 |6 505-01  |a 1.5 Thioether Ligation1.6 Thioester Ligation; 1.6.1 Native Chemical Ligation (NCL); 1.6.2 Expressed Protein Ligation (EPL); 1.6.3 Thioacid-Mediated Ligation Strategies; 1.7 α-Ketoacid-Hydroxylamine (KAHA) Ligation; 1.7.1 Acyltrifluoroborates and Hydroxylamines Ligation; 1.8 Staudinger Ligation; 1.9 Azide-Alkyne Cycloaddition; 1.10 Diels-Alder Ligation; References; Chapter 2 Protein Chemical Synthesis by SEA Ligation; 2.1 Introduction; 2.2 Essential Chemical Properties of SEA Group; 2.3 Protein Total Synthesis Using SEA Chemistry -- SEAon/off Concept; 2.3.1 Synthesis of SEAoff Peptide Segments. 
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952 f f |a Middle Tennessee State University  |b Main  |c James E. Walker Library  |d Electronic Resources  |t 0  |e QP551 .C44 2017  |h Library of Congress classification