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Glossary of peptide terminology (revision 15)

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Glossary of peptide terminologyReference material
ScopeTerms used across this wiki
ArrangementBy domain, then alphabetically
List infobox · conventions

This glossary defines terms used across PeptidePedia Wiki. Each entry gives a short definition and, where a full article exists, links to it. Terms are grouped by domain and ordered alphabetically within each group.[1]

Definitions here are deliberately brief. Where a term carries a distinction that matters — purity against content, sterility against endotoxin freedom, contraindication against warning — the entry states the distinction and the article develops it.[2]

The glossary is not a substitute for the articles and does not attempt completeness.[3]

Chemistry and manufacture

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Aib
α-aminoisobutyric acid, a non-proteinogenic residue used to block DPP-4 cleavage.
Acylation
Attachment of a fatty acid to a peptide, usually for albumin binding.
Crude
The material obtained directly after cleavage, before purification. See Crude peptide.
Deletion sequence
A synthesis by-product missing one or more residues.
Fmoc
The base-labile temporary protecting group scheme dominating peptide synthesis.
Linker
The resin attachment defining the C-terminal functionality of the finished peptide.
Lyophilisation
Freeze-drying; the isolation step producing the powder in a vial. See Lyophilisation.
SPPS
Assembly of a peptide on an insoluble support.
TFA salt
The salt form in which most reverse-phase-purified peptides are isolated.[1]

Analysis and documentation

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Area percent
Main-peak area over total integrated area; normalised, and independent of quantity.
Batch number
The identifier linking a container to production records.
COA
The document a supplier issues reporting determinations on a lot.
Endotoxin
Lipopolysaccharide from Gram-negative bacteria; survives sterilisation.
Karl Fischer
A water-specific determination, as distinct from loss on drying.
LOD
The lowest level at which presence can be distinguished from background.
Peptide content
The mass fraction of a solid that is peptide; not purity.
Reference standard
A characterised material of assigned content used for calibration.
Retention time
Time from injection to peak; characteristic under fixed conditions.
Stability-indicating
Of a method, able to resolve degradation products from the parent.[2]

Clinical and evidence

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Placebo-adjusted
The difference between treatment and comparator arms.
ITT
Analysis by randomised assignment, regardless of treatment received.
NNT
Reciprocal of the absolute risk reduction, over a stated period.
Surrogate endpoint
A measure standing in for an outcome of direct importance.
Estimand
A precise statement of the quantity a trial estimates, including how discontinuation is handled.
Contraindication
A circumstance in which labelling directs a product is not used; distinct from a warning.
Research use only
A presentation, not a quality grade; such material is not approved for human use.[4]

Additional terms are defined where they first appear in the articles. Suggestions for entries belong on the talk page.[3]

See also

References

  1. ^ a b United States Pharmacopeia, General Chapter <1503>, Quality Attributes of Synthetic Peptide Drug Substances.
  2. ^ a b United States Pharmacopeia, General Chapter <621>, Chromatography.
  3. ^ a b PeptidePedia Wiki community test-report tally, 2024–2026 (self-reported; see Project:Sourcing guidelines).
  4. ^ Drucker DJ. "Mechanisms of action and therapeutic application of glucagon-like peptide-1." Cell Metabolism 27(4):740–756 (2018). PMID 29617641.