TY - JOUR
T1 - The octanoylated energy regulating hormone ghrelin
T2 - An expanded view of ghrelin’s biological interactions and avenues for controlling ghrelin signaling
AU - Cleverdon, Elizabeth R.
AU - McGovern-Gooch, Kayleigh R.
AU - Hougland, James L.
N1 - Publisher Copyright:
© 2017 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2016/11/16
Y1 - 2016/11/16
N2 - Ghrelin is a small peptide hormone that requires a unique post-translational modification, serine octanoylation, to bind and activate the GHS-R1a receptor. Initially demonstrated to stimulate hunger and appetite, ghrelin-dependent signaling is implicated in a variety of neurological and physiological processes influencing diseases such as diabetes, obesity, and Prader-Willi syndrome. In addition to its cognate receptor, recent studies have revealed ghrelin interacts with a range of binding partners within the bloodstream. Defining the scope of ghrelin’s interactions within the body, understanding how these interactions work in concert to modulate ghrelin signaling, and developing molecular tools for controlling ghrelin signaling are essential for exploiting ghrelin for therapeutic effect. In this review, we discuss recent findings regarding the biological effects of ghrelin signaling, outline binding partners that control ghrelin trafficking and stability in circulation, and summarize the current landscape of inhibitors targeting ghrelin octanoylation.
AB - Ghrelin is a small peptide hormone that requires a unique post-translational modification, serine octanoylation, to bind and activate the GHS-R1a receptor. Initially demonstrated to stimulate hunger and appetite, ghrelin-dependent signaling is implicated in a variety of neurological and physiological processes influencing diseases such as diabetes, obesity, and Prader-Willi syndrome. In addition to its cognate receptor, recent studies have revealed ghrelin interacts with a range of binding partners within the bloodstream. Defining the scope of ghrelin’s interactions within the body, understanding how these interactions work in concert to modulate ghrelin signaling, and developing molecular tools for controlling ghrelin signaling are essential for exploiting ghrelin for therapeutic effect. In this review, we discuss recent findings regarding the biological effects of ghrelin signaling, outline binding partners that control ghrelin trafficking and stability in circulation, and summarize the current landscape of inhibitors targeting ghrelin octanoylation.
KW - Ghrelin
KW - ghrelin O-acyltransferase
KW - ghrelin O-acyltransferase inhibitors
KW - protein acylation
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U2 - 10.1080/09687688.2017.1388930
DO - 10.1080/09687688.2017.1388930
M3 - Review article
AN - SCOPUS:85036659942
SN - 0968-7688
VL - 33
SP - 111
EP - 124
JO - Molecular Membrane Biology
JF - Molecular Membrane Biology
IS - 6-8
ER -