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Chemical synthesis and structural analysis of guanylate cyclase C agonist linaclotide 被引量:1
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作者 Chenchen Chen Shuai Gao +3 位作者 Qian Qu Pengcheng Mi Anjin Tao Yi-Ming Li 《Chinese Chemical Letters》 SCIE CAS CSCD 2018年第7期1135-1138,共4页
Guanylate cyclase C(GC-C) is an important receptor protein expressed by intestinal epithelial cells, and its dysregulation leads to severe intestinal diseases. Linaclotide is a 14-amino acid peptide approved by the FD... Guanylate cyclase C(GC-C) is an important receptor protein expressed by intestinal epithelial cells, and its dysregulation leads to severe intestinal diseases. Linaclotide is a 14-amino acid peptide approved by the FDA for the treatment of irritable bowel syndrome with constipation(IBS-C), which activates guanylate cyclase C to accelerate intestinal transit. Drug molecule design based on structural information plays a crucial role and the activity of linaclotide still need to improve, while the structure of linaclotide remains unknown. In this work, linaclotide and its D-enantiomer were obtained through Fmoc solid phase peptide synthesis method and co-crystalized through racemic crystallization. The crystal structure showed that linaclotide has a tight, three-beta turns structure immobilized by three pairs of disulfide bonds. 展开更多
关键词 Linaclotide Guanylyl cyclase Protein chemical synthesis fmoc solid phase peptide synthesis Racemic crystallization
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