TY - JOUR
T1 - Neuropeptide biosynthesis
T2 - focus on the carboxypeptidase processing enzyme
AU - Fricker, Lloyd D.
PY - 1985
Y1 - 1985
N2 - Many peptide neurotransmitters and hormones are initially synthesized as large protein precursors (prohormones) which must undergo proteolytic processing to yield the biologically active fragment. Often, the neurotransmitter or hormone is flanked by pairs of basic amino acids in the precursor molecule, and the sequential action of a trypsin-like endopeptidase followed by a carboxypeptidase-B-like exopeptidase would liberate the hormone. An important question is whether unique enzymes are associated with each prohormone, or whether general processing enzymes perform similar cleavages for all prohormones. Recent studies on the carboxypeptidase-B-like processing enzyme associated with enkephalin biosynthesis suggests that this enzyme is also involved in the biosynthesis of many other peptide hormones and neurotransmitters.
AB - Many peptide neurotransmitters and hormones are initially synthesized as large protein precursors (prohormones) which must undergo proteolytic processing to yield the biologically active fragment. Often, the neurotransmitter or hormone is flanked by pairs of basic amino acids in the precursor molecule, and the sequential action of a trypsin-like endopeptidase followed by a carboxypeptidase-B-like exopeptidase would liberate the hormone. An important question is whether unique enzymes are associated with each prohormone, or whether general processing enzymes perform similar cleavages for all prohormones. Recent studies on the carboxypeptidase-B-like processing enzyme associated with enkephalin biosynthesis suggests that this enzyme is also involved in the biosynthesis of many other peptide hormones and neurotransmitters.
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U2 - 10.1016/0166-2236(85)90081-5
DO - 10.1016/0166-2236(85)90081-5
M3 - Review article
AN - SCOPUS:0022259540
SN - 0378-5912
VL - 8
SP - 210
EP - 214
JO - Trends in Neurosciences
JF - Trends in Neurosciences
IS - C
ER -