SYNTHESIS AND BIOLOGICAL-ACTIVITY OF GLYCOSYLATED ANALOGS OF SOMATOSTATIN

被引:10
作者
LAVIELLE, S [1 ]
LING, N [1 ]
BRAZEAU, P [1 ]
BENOIT, R [1 ]
WASADA, T [1 ]
HARRIS, D [1 ]
UNGER, R [1 ]
GUILLEMIN, R [1 ]
机构
[1] UNIV TEXAS,HLTH SCI CTR,SW MED SCH,DALLAS,TX 75235
基金
美国国家卫生研究院;
关键词
D O I
10.1016/0006-291X(79)91566-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The synthesis by solid-phase methodology of two glycosylated analogs of somatostatin [Glc-Asn5]-SS and [NAcGlc-Asn5]-SS is described. These two analogs have been biologically tested on the secretion of pituitary growth hormone, pancreatic glucagon and insulin. The results show that glycosylation of somatostatin on the Asn5 residue decreases by a hundred fold the inhibition activity on GH release when tested invitro. Invivo, since the activity is similar to somatostatin the carbohydrates are probably removed by some enzymatic reaction and thus liberate the full activity of somatostatin. © 1979.
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页码:614 / 622
页数:9
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