Searching for Merrifield Solid Support Peptide Synthesis information? Find all needed info by using official links provided below.
https://en.chem-station.com/reactions-2/2014/02/merrifield-solid-phase-peptide-synthesis.html
Feb 02, 2014 · Solid phase peptide synthesis (SPPS), developed by R. B. Merrifield, was a major breakthrough allowing for the chemical synthesis of peptides and small proteins. SPPS results in high yields of pure products and works more quickly than classical synthesis (liquid-phase peptide synthesis, LPPS). The advantages of this method are very considerable.4.5/5(9)
https://chem.libretexts.org/Courses/Athabasca_University/Chemistry_360%3A_Organic_Chemistry_II/Chapter_26%3A_Biomolecules%3A_Amino_Acids%2C_Peptides%2C_and_Proteins/26.08_Automated_Peptide_Synthesis%3A_The_Merrifield_Solid-Phase_Technique
The solid‑phase used in this method is a polymer support. You will not be examined on the details of the Merrifield solid‑phase method; however, you should be prepared to write a couple of paragraphs describing this important process. For his work on the synthesis of peptides, Bruce Merrifield was awarded the 1984 Nobel Prize in chemistry.
https://en.wikipedia.org/wiki/Solid-phase_synthesis
The process was originally developed in the 1950s and 1960s by Robert Bruce Merrifield in order to synthesise peptide chains, and which was the basis for his 1984 Nobel Prize in Chemistry. In the basic method of solid-phase synthesis, building blocks that have two functional groups are used.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3564544/
In the early 1960s, Merrifield proposed the use of a polystyrene-based solid support for peptide synthesis. Peptides could be assembled stepwise from the C to N terminus using N α-protected amino acids.SPPS of a tetrapeptide was achieved by using Cbz as an α-amino-protecting group, coupling with N,N'-dicyclohexylcarbodiimide (DCC), and liberating the peptide from the support by ...Cited by: 20
https://www.peptide.com/resources/peptide-synthesis-resins/
PAM resin is widely used for solid phase synthesis of peptides utilizing the Boc strategy. The numerous Boc deprotection reactions with trifluoroacetic acid (TFA) required in the synthesis of large peptides leads to significant losses of peptide from Merrifield resin. 1 PAM resin provides better stability to TFA, 2 but the finished products are harder to cleave.
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