Literature DB >> 3473964

The role of secretory granules in peptide biosynthesis.

R E Mains, E I Cullen, V May, B A Eipper.   

Abstract

There are many events in the posttranslational processing of bioactive peptides that occur in secretory granules and not to any great extent in other cellular organelles and that do not appear as modifications of the structure of many conventional neurotransmitters. In addition, at least two very important steps are unique to peptide-containing granules: (1) the peptides must begin their trek to the secretory granule in the RER as a larger precursor, rather than being taken up as a finished or nearly finished product into a mature granule; (2) there is at least one crucial sorting step on the way from the RER to the secretory granule that must occur faithfully before the peptide correctly appears in the granule. As for small molecules such as the catecholamines, the posttranslational processing enzymes and any required cofactors must also be put into the granules if the final events of processing are to occur with fidelity. Many of the posttranslational processing enzymes are only beginning to be identified. It is clear from these studies on purified PAM and peptide alpha-amidation as it occurs in cells that correlating test tube studies with the functioning of secretory granules is a worthwhile, if difficult, pursuit. The unique milieu inside the granule is difficult to mimic in a test tube. Transfection of peptide-producing cells with cDNAs encoding precursors with specific alterations in processing sites offers perhaps the best way to interface the studies of secretory granules and the posttranslational processing enzymes that mediate those functions.

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Year:  1987        PMID: 3473964     DOI: 10.1111/j.1749-6632.1987.tb27213.x

Source DB:  PubMed          Journal:  Ann N Y Acad Sci        ISSN: 0077-8923            Impact factor:   5.691


  14 in total

1.  Multiple episodes of induced secretion of human growth hormone from recombinant AtT-20 cells.

Authors:  A Sambanis; G Stephanopoulos; H F Lodish
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2.  In vitro aggregation of the regulated secretory protein chromogranin A.

Authors:  Renu K Jain; Wen Tzu Chang; Chitta Geetha; Paul B M Joyce; Sven-Ulrik Gorr
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Review 3.  How peptidergic neurons cope with variation in physiological stimulation.

Authors:  I G Morgan; I W Chubb
Journal:  Neurochem Res       Date:  1991-06       Impact factor: 3.996

4.  Posttranslational processing of endogenous and of baculovirus-expressed human gastrin-releasing peptide precursor.

Authors:  A M Lebacq-Verheyden; P G Kasprzyk; M G Raum; K Van Wyke Coelingh; J A Lebacq; J F Battey
Journal:  Mol Cell Biol       Date:  1988-08       Impact factor: 4.272

5.  Cultivation of recombinant, insulin-secreting AtT-20 cells as free and entrapped spheroids.

Authors:  K K Papas; I Constantinidis; A Sambanis
Journal:  Cytotechnology       Date:  1993       Impact factor: 2.058

Review 6.  Sorting and processing of secretory proteins.

Authors:  P A Halban; J C Irminger
Journal:  Biochem J       Date:  1994-04-01       Impact factor: 3.857

7.  Endocytotic pathways in the melanotroph of the rat pituitary.

Authors:  N Bäck; S Soinila; I Virtanen
Journal:  Histochem J       Date:  1993-02

Review 8.  Mass Spectrometry Approaches Empowering Neuropeptide Discovery and Therapeutics.

Authors:  Krishna D B Anapindi; Elena V Romanova; James W Checco; Jonathan V Sweedler
Journal:  Pharmacol Rev       Date:  2022-07       Impact factor: 18.923

9.  Localization of cholecystokinin-like and calcitonin-like peptides in infant carotid bodies: a light- and electron-microscopic immunohistochemical study.

Authors:  Y Y Wang; D G Perrin; E Cutz
Journal:  Cell Tissue Res       Date:  1993-04       Impact factor: 5.249

10.  Ionic milieu controls the compartment-specific activation of pro-opiomelanocortin processing in AtT-20 cells.

Authors:  W K Schmidt; H P Moore
Journal:  Mol Biol Cell       Date:  1995-10       Impact factor: 4.138

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