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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 366410Generated: October 25, 2026

Trifluoroacetic acid → L-Glutamic Acid

https://huagongshe.com/reaction/366410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantTris(hydroxymethyl)aminomethaneHCID 6503—
ReactantCalcium ChlorideHCID 5284359—
ReactantTFA acetonitrileHCID 21924481—
ProductL-Glutamic AcidHCID 33032—

Reaction Steps

The oligopeptides prepared as described in Example 2 were individually dissolved in PSA digestion buffer (12 mM tris(hydroxymethyl)-aminomethane pH8.0, 25 mM NaCl, 0.5 mM CaCl2) and the solution added to PSA at a molar ration of 100 to 1. The reaction is quenched after various reaction times by the addition of trifluoroacetic acid (TFA) to a final 1% (volume/volume). The quenched reaction was analyzed by HPLC on a reversed-phase C18 column using an aqueous 0.1% TFA/acetonitrile gradient. The results of the assessment are shown in FIG. 2. Other oligopeptides prepared as described in Example 2 were tested in the same assay wherein the reaction was quenched at 4 hours. Those results of the assessment are shown in FIG. 3. The removal of an asparagine residue from the amino terminus of the oligopeptide results in a significant loss of PSA mediated peptide hydrolysis, while the presence of a glutamic acid residue at the carboxyl end of the peptide appears not to be essential to recognition by PSA.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06130204
Source datasetuspto-grants-2000_10
ORD IDord-2d806cedacd44f0a90f1cba3cdbe959e
Source noteuspto-grants-2000_10