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Solid-phase peptide synthesis: difference between revisions

Diff·revision 6 → 7·01:38, 13 Aug 2024

Difference between revision 6 and revision 7 of Solid-phase peptide synthesis. 2 lines changed; the page grew by 324 bytes.

Revision 6 — 19:37, 31 Jul 2024
SemaglutideSasha (talk)
rm the vendor-specific packaging detail; not general enough for the article
2,254 bytes +361
Revision 7 — 01:38, 13 Aug 2024
RepackRadek (talk)
correct the freezer temperature range given for long-term storage
2,578 bytes +324
11The cycle is: remove the temporary N-terminal protecting group, wash, couple the next protected amino acid in excess, wash. Excess reagent drives each coupling towards completion, and the washing that removes it is the operation solution-phase synthesis cannot perform cheaply.{{r|behrendt2016}}11The cycle is: remove the temporary N-terminal protecting group, wash, couple the next protected amino acid in excess, wash. Excess reagent drives each coupling towards completion, and the washing that removes it is the operation solution-phase synthesis cannot perform cheaply.{{r|behrendt2016}}
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+13Its principal limitation follows from the same design. Intermediates cannot be purified — everything anchored to the resin travels together — so a failed coupling generates a deletion sequence that persists to the end and must be separated at the [[Preparative HPLC purification|purification]] stage.{{r|behrendt2016}}
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13== Support and linker ==15== Support and linker ==
14The resin is typically cross-linked polystyrene or a polyethylene glycol–polystyrene composite, functionalised with a linker that attaches the first residue and defines how the finished peptide is released.{{r|behrendt2016}}16The resin is typically cross-linked polystyrene or a polyethylene glycol–polystyrene composite, functionalised with a linker that attaches the first residue and defines how the finished peptide is released.{{r|behrendt2016}}