Title of article :
Characterization of Nα-acetyl methionyl human growth hormone formed during expression in Saccharomyces cerevisiae with liquid chromatography and mass spectrometry
Author/Authors :
Jung، نويسنده , , Chulho and Lee، نويسنده , , Young-Phil and Jeong، نويسنده , , Yeong Ran and Kim، نويسنده , , Jin Young and Kim، نويسنده , , Young Hwan and Kim، نويسنده , , Hyun Sik، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2005
Pages :
7
From page :
53
To page :
59
Abstract :
We found a new variant of human growth hormone (hGH) from the recombinant hGH expression process in Saccharomyces cerevisiae. The variant was identified as Nα-acetyl methionyl hGH which may be formed by Nα-acetylation of met-hGH during the intracellular expression of hGH in S. cerevisiae. The variant was isolated from manufacturing process of LG Life Sciences’ hGH product. The variant was subjected to trypsin digestion and RP-HPLC analysis, resulting in a delayed retention time and an increased mass (173 Da) of T1 tryptic peptide. The amino acid composition and amino acid sequence of the peptide showed the same result with T1 peptide of met-hGH except the N-terminal modification on methionine in the variant peptide. With collision induced dissociation (CID) experiments of the variant T1 tryptic peptide, we found the sequence and the a1 fragment of N-terminal residue matched with those of acetyl-methionyl hGH. Within our production process, we produce the methionyl hGH first and then use the aminopeptidase to cut the N-terminal methionine. So the acetylation may inhibit the aminopeptidase to remove methionine and produces Nα-acetyl methionyl hGH. And the biological activity of the variant was comparable to one of the unmodified hGH when tested by rat weight gain bioassay.
Keywords :
variant , mass spectrometry , Aminopeptidase , Human growth hormone , modification
Journal title :
Journal of Chromatography B
Serial Year :
2005
Journal title :
Journal of Chromatography B
Record number :
1457118
Link To Document :
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