Chemical Protein Synthesis
| Korporativní autor: | |
|---|---|
| Další autoři: | |
| Shrnutí: | XI, 259 p. 89 illus., 69 illus. in color. text |
| Jazyk: | angličtina |
| Vydáno: |
New York, NY :
Springer US : Imprint: Humana,
2022.
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| Vydání: | 1st ed. 2022. |
| Edice: | Methods in Molecular Biology,
2530 |
| Témata: | |
| On-line přístup: | https://doi.org/10.1007/978-1-0716-2489-0 |
| Médium: | Elektronický zdroj Kniha |
Obsah:
- Sulfated Glycoprotein Synthesis
- Total Chemical Synthesis of a SARS-CoV-2 Miniprotein Inhibitor LCB1
- Serine/Threonine Ligation and Cysteine/Penicillamine Ligation
- Continuous-flow synthesis of N-Methylated Peptides via Generation of an Acyl N-Methylimidazolium Cation
- Covalent Reactive Peptides to Block Protein – Protein Interactions and Inhibit Microbe-Host Interaction
- Ynamide-Mediated Synthetic Approach to Thioamide Substituted Peptides
- Improved Handling of Peptide Segments Using Side Chain-Based “Helping Hand” Solubilizing Tools
- Helical Stabilization of Peptide Macrocycles by Stapled Architectures
- General solution to the preparation of ꞵ-thiolated/Selenolated Amino Acids Via Visible Light Catalyzed Asymmetric Giese reaction
- Side-chain Anchoring Strategies for the Synthesis of Peptide Thioesters and Selenoesters
- Preparation of Site-Specific Succinylated Histone Mimics to Investigate ItsImpact On Nucleosome Dynamics
- Protein Synthesis Via Activated Cysteine-Directed Protein Ligation
- Sulfonium Tethered Peptide
- PAL-mediated Ligation for Protein and Cell-Surface Modification
- Development of a Glycoform Library-based Strategy to Decipher the Role of Protein Glycosylation
- A Selenium-Based Cysteine Surrogate for Protein Chemical Synthesis
- Removable Backbone Modification (RBM) Strategy for the Chemical Synthesis of Hydrophobic Peptides/Proteins. .