## Abstract Using a solution of [^35^S]‐phenylisothiocyanate in pentane with a specific activity of 30 to 8O mC/mmole, the authors have determined the sequence of di‐, tri‐peptides and a pentapeptide on the following quantities: 1 to 2 nmole of peptide when the [^35^S]‐phenylthiohydantoines obtaine
Etude de structures peptidiques à l'aide de phénylisothiocyanate III. Sur la formation des phénylthiohydantoïnes-[35S] et sur leur chromatographie sur papier
✍ Scribed by Emile Cherbuliez; A. R. Sussmann; J. Rabinowitz
- Publisher
- John Wiley and Sons
- Year
- 1961
- Tongue
- German
- Weight
- 290 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
By the analysis of di‐, tri‐peptides and a pentapeptide of known constitution the authors show that using an N,N‐dimethylformamide solution of [^35^S]‐phenylisothiocyanate with a spectific activity of 10 to 40 mc/mmole the sequence of amino acids can be determined starting with 0,005 micromole of peptide.
📜 SIMILAR VOLUMES
## Abstract The microchromatography of phenylthiohydantoins on thin layers of silica (solvent: heptane, pyridine, ethyl acetate 5:3:2 vol.; revelation by starch‐iodineazide) is described. This method is 10 to 20 times more sensitive than that of classic paper chromatography. Good results are obtain
t i l'aide de phenylisothiocyanate VII [ill) Sur la reaction de quelques acides aminks et de quelques thiols avec le phenylisothiocyanate
## Abstract The authors describe modified procedures for the synthesis of phenylthiohydantoins derived from α‐amino acids, applied to 16 amino acids. With the exception of the phenylthiohydantoins containing a free NH~2~, CONH~2~, COOH or hetero‐cyclic group belonging to the starting amino acid,