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Liquid chromatography-mass spectrometry: difference between revisions

Diff·revision 8 → 9·18:12, 10 Jan 2025

Difference between revision 8 and revision 9 of Liquid chromatography-mass spectrometry. 6 lines changed; the page grew by 673 bytes.

Revision 8 — 05:03, 24 Dec 2024
AnalyticalAnnie (talk)
add the figure for the chromatogram and caption its axes
2,642 bytes ±0
Revision 9 — 18:12, 10 Jan 2025
NauseaNoor (talk)
clarify the difference between related substances and total impurities
3,315 bytes +673
1{{Infobox method1{{Infobox method
2| name = Liquid chromatography-mass spectrometry2| name = Liquid chromatography-mass spectrometry
+3| subtitle = Hyphenated technique
3| Abbreviation = LC-MS4| Abbreviation = LC-MS
4| Combines = Chromatographic separation and mass detection5| Combines = Chromatographic separation and mass detection
1920
20Tandem operation — selecting a precursor, fragmenting it, and measuring the fragments — adds sequence information and can locate a modification to a residue rather than merely detecting it.{{r|aebersold2003}}21Tandem operation — selecting a precursor, fragmenting it, and measuring the fragments — adds sequence information and can locate a modification to a residue rather than merely detecting it.{{r|aebersold2003}}
+22
+23== Quantification ==
+24LC-MS is not inherently quantitative: ionisation efficiency varies by orders of magnitude between species and with what else is eluting. Quantification requires calibration against a standard of the same substance, ideally with an isotopically labelled internal standard.{{r|aebersold2003}}
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+26This is why a purity figure is normally reported from ultraviolet detection rather than from mass detection: ultraviolet response at 214 nm is roughly proportional to the number of peptide bonds and is therefore a reasonable proxy for mass across related peptides, whereas mass-spectrometric response is not.{{r|usp1503}}
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22== References ==28== References ==