A Modular Customizable Ligand-Conjugate (LC) System Targeting Ghrelin O-Acyltransferase

被引:0
|
作者
Ford, Amber L. [1 ]
Taft, Caine W. [1 ]
Sprague-Getsy, Andrea M. [1 ]
Carlson, Gracie C. [1 ]
Mate, Nilamber A. [1 ]
Sieburg, Michelle A. [1 ]
Chisholm, John D. [1 ,2 ]
Hougland, James L. [1 ,2 ,3 ]
机构
[1] Syracuse Univ, Dept Chem, Syracuse, NY 13244 USA
[2] Syracuse Univ, BioInspired Syracuse, Syracuse, NY 13244 USA
[3] Syracuse Univ, Dept Biol, Syracuse, NY 13244 USA
基金
美国国家科学基金会; 美国国家卫生研究院;
关键词
ghrelin; ghrelin <italic>O</italic>-acyltransferase; membrane-bound <italic>O</italic>-acyltransferase; GHSR; posttranslational modification; membrane enzyme; protein acylation; peptide mimetic inhibitor; HORMONE SECRETAGOGUE RECEPTOR; PROSTATE-CANCER; ANOREXIA-NERVOSA; PREPROGHRELIN ISOFORM; BREAST-CANCER; PEPTIDE; EXPRESSION; IDENTIFICATION; SUBSTRATE; ANTIBODY;
D O I
10.3390/biom15020204
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
Ghrelin is a 28 amino acid peptide hormone that impacts a wide range of biological processes, including appetite regulation, glucose metabolism, growth hormone regulation, and cognitive function. To bind and activate its cognate receptor, ghrelin must be acylated on a serine residue in a post-translational modification performed by ghrelin O-acyltransferase (GOAT). GOAT is a membrane-bound O-acyltransferase (MBOAT) responsible for the catalysis of the addition of an octanoyl fatty acid to the third serine of desacyl ghrelin. Beyond its canonical role for ghrelin maturation in endocrine cells within the stomach, GOAT was recently reported to be overexpressed in prostate cancer (PCa) cells and detected at increased levels in the serum and urine of PCa patients. This suggests GOAT can serve as a potential route for the detection and therapeutic targeting of PCa and other diseases that exhibit GOAT overexpression. Building upon a ghrelin mimetic peptide with nanomolar affinity for GOAT, we developed an antibody-conjugate-inspired system for customizable ligand-conjugate (LC) synthesis allowing for the attachment of a wide range of cargoes. The developed synthetic scheme allows for the easy synthesis of the desired LCs and demonstrates that our ligand system tolerates an extensive palette of cargoes while maintaining nanomolar affinity against GOAT.
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页数:17
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