Source: Vy M. Dong and Diane Le, Department of Chemistry, University of California, Irvine, CA
Merrifield's solid-phase synthesis is a Nobel Prize winning invention where a reactant molecule is bound on a solid support and undergoes successive chemical reactions to form a desired compound. When the molecules are bound to a solid support, excess reagents and byproducts can be removed by washing away the impurities, while the target compound remains bound to the resin. Specifically, we will showcase an example of solid-phase peptide synthesis (SPPS) to demonstrate this concept.
Procedure
1. Loading the Resin
To a 100mL peptide synthesis vessel, add 2-chlorotrityl chloride (CTC) resin (1.1 mmol/g, 0.360 g, 0.400 mmol). Add 20 mL DMF and allow them to swell for 30 min under N2.
Drain the beads under vacuum and add 10 mL DMF.
Add 500 mg Fmoc-Ala-OH (1.60 mmol) and 2.5 mL i-Pr2EtN, and mix under N2 for 15 min.
Drain the solvent under vacuum and repeat the loading with Fmoc-Ala-OH for 15 min.
Drain the solvent under
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Resultaten
Representative results for solid phase peptide synthesisfor Procedure 3.
Procedure Step
Color of solution
3.1
Control - Clear, light yellow
Reaction – Clear, light yellow
3.2
Control - Clear, light yellow
Reaction – Dark blue
3.3
Dark blue solution, beads blue – c
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Toepassing en samenvatting
In this experiment, we have demonstrated an example of solid-phase synthesis via SPPS through the synthesis of a dipeptide.
Solid-phase synthesis is widely used in combinatorial chemistry to build up libraries of compounds for rapid screening. It has been commonly used to synthesize peptides, oligosaccharides, and nucleic acids. Moreover, this concept has been implemented in chemical synthesis. Because it is heterogeneous, these solid-supported reagents can often be recycled and reused in subs
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To a 100mL peptide synthesis vessel, add 2-chlorotrityl chloride (CTC) resin (1.1 mmol/g, 0.360 g, 0.400 mmol). Add 20 mL DMF and allow them to swell for 30 min under N2.
Drain the beads under vacuum and add 10 mL DMF.
Add 500 mg Fmoc-Ala-OH (1.60 mmol) and 2.5 mL i-Pr2EtN, and mix under N2 for 15 min.
Drain the solvent under vacuum and repeat the loading with Fmoc-Ala-OH for 15 min.
Drain the solvent under vacuum and wash the beads with 10 mL DMFunder N2, and drain under vacuum 3x.
2. Deprotection of the Fmoc Group
Add 10 mL 20% 4-methylpiperidine in DMF and stir the beads under N2 for 15 min.
Drain the solvent under vacuum and repeat the deprotection.
Wash the beads with 10 mL DMF under N2 and drain under vacuum 3x.
3. Performing the Kaiser Test
Perform the Kaiser test by adding 1-2 drops of solution A (0.5 mL 0.01 M KCN, 24.5 mL pyridine), solution B (1 g ninhydrin, 20 mL n-butanol), and solution C (20 g phenol, 10 mL n-butanol) each into two test tubes. One test tube will be the control while the other will monitor the reaction.
Add a few beads of the resin from the reaction vessel to reaction test tube and heat up the two test tubes to 110 °C.
If the deprotection is complete, the contents of the test tube will turn a dark blue/purple color. If the deprotection is incomplete or failed, the solution will remain yellow. Compare the reaction test tube with the control test tube.
4. Coupling the Next Building Blocks
Drain the solvent under vacuum.
Wash the beads with 10 mL N-methyl-2-pyrrolidone under N2 and drain the solvent under vacuum.
To begin the next coupling, add 10 mL NMP, 620 mgFmoc-Phe-OH (1.6 mmol), 610 mg HBTU (1.6 mmol), and 2.5 mLi-Pr2EtN, and allow the resin to bubble under N2 for 30 min.
Drain the solvent under vacuum.
Wash the beads with 10 mL DMF under N2 and drain under vacuum 3x.
Perform the Kaiser test (see steps 3.1-3.3) to look for the completion of the coupling. The beads and solution in the test tube should be yellow.
5. Cleaving the Peptide Off the Resin
Cleave the remaining Fmoc group using steps 2.1-2.3.
After the solvent is drained under vacuum, add 40 mL cleavage solution (95% TFA, 2.5% H2O, 2.5% TIPS) to the resin and bubble under N2 for 3 h.
Place a new receiving flask on the peptide synthesizer and drain theTFA solution containing the desired peptide under vacuum into the new flask.
6. Precipitation and I solation of the Peptide
Separate the TFA solution into 4 conical vials and add 25 mL cold ether (−20 °C) to each vial to precipitate the peptide.
Centrifuge the vials (3,000 rpm, 0-4 °C) for 20 min. Decant the remaining TFA and ether solution from the conical vials and concentrate the peptide precipitate to afford the desired dipeptide as a white solid.
