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Synthesis and immunological evaluation of the conjugates composed from a muramyl peptide GMDP and tuftsin.
Titov, V M; Meshcheryakova, E A; Balashova, T A; Andronova, T M; Ivanov, V T.
Affiliation
  • Titov VM; Laboratory of Peptide Chemistry, Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Moscow, Russia.
Int J Pept Protein Res ; 45(4): 348-55, 1995 Apr.
Article in En | MEDLINE | ID: mdl-7601608
The conjugates of a muramyl dipeptide analog GMDP (N-acetylglucosaminyl beta 1-->4 N-acetylmuramyl-L-alanyl-D-isoglutamine) and tuftsin (Thr-Lys-Pro-Arg) were synthesized from unprotected GMDP by mixed anhydride procedure. The identity of the conjugates was confirmed by high resolution NMR and their immunomodulating properties were determined in various tests. It was found that the conjugate in which the GMDP carboxyl group forms an amide bond with the epsilon-amino group of tuftsin lysyl residue exceeds GMDP in all the activities determined. Synergism of GMDP and tuftsin was found in phagocytosis stimulation assay.
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Collection: 01-internacional Database: MEDLINE Main subject: Tuftsin / Acetylmuramyl-Alanyl-Isoglutamine Limits: Animals Language: En Journal: Int J Pept Protein Res Year: 1995 Document type: Article Affiliation country: Russia Country of publication: Denmark
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Collection: 01-internacional Database: MEDLINE Main subject: Tuftsin / Acetylmuramyl-Alanyl-Isoglutamine Limits: Animals Language: En Journal: Int J Pept Protein Res Year: 1995 Document type: Article Affiliation country: Russia Country of publication: Denmark