Abstract
This chapter provides an overview of peptide synthesis giving emphasis on solid-phase peptide synthesis (SPPS). Currently, most of the peptides used for research or therapeutics are synthesized by SPPS methods. Successful peptide synthesis overcoming the usual handles and limitations is extremely dependent on the convenient selection of resins, linkers, amino acid derivatives, and coupling reagents as well as side chain (de)protection and cleavage conditions. Old and newer solid supports, linkers, protecting groups, coupling reagents, deprotection, and/or cleavage solutions widely used in Fmoc/. tBu methodology are presented and discussed. Newer greener ways of synthesis are also presented. The chapter concludes with future challenges, perspectives and opportunities in the field of solid-phase peptide chemistry.
Original language | English |
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Title of host publication | Peptide Applications in Biomedicine, Biotechnology and Bioengineering |
Publisher | Elsevier Inc. |
Pages | 1-21 |
Number of pages | 21 |
ISBN (Electronic) | 9780081007426 |
ISBN (Print) | 9780081007365 |
DOIs | |
Publication status | Published - 16 Nov 2017 |
Keywords
- Cleavage solution
- Coupling reagents
- Cyclization reagents
- Disulfide formation
- Fmoc/tBu methodology
- Linkers
- Solid-phase peptide synthesis
- SPPS