Abstract
Peptide hormones are post-translationally matured before they reach a structure in which they can fulfill their biological functions. The prohormone processing may encompass a variety of endoproteolytic cleavages, N- and C-terminal trimmings, and amino acid derivatizations. The same prohormone can be variably processed in different cell types and, in addition, diseased cells often change the processing of a given precursor. The translational process is often either increased or decreased in diseased cells, which renders the ensuing modifications of the prohormone incomplete. Consequently, a variable mixture of precursors and processing-intermediates accumulates in plasma. In order to exploit disturbed posttranslational processing for diagnostic use and at the same time provide an accurate measure of the translational product, a simple analytical principle named "processing-independent analysis" (PIA) was designed. PIA-methods quantitate the total mRNA product irrespective of the degree of processing. PIA-methods have now been developed for a number of prohormones and proteins, and their diagnostic potential appears promising in diagnosis of cardiovascular disease and in several malignancies.
Original language | English |
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Journal | Frontiers in bioscience : a journal and virtual library |
Volume | 17 |
Pages (from-to) | 1804-15 |
Number of pages | 12 |
Publication status | Published - 2012 |
Keywords
- Amino Acid Sequence
- Gene Expression
- Hormones
- Humans
- Molecular Sequence Data
- Peptides
- Protein Processing, Post-Translational
- Sequence Homology, Amino Acid