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Mass spectrometry: difference between revisions

Diff·revision 1 → 2·19:05, 30 Jun 2024

Difference between revision 1 and revision 2 of Mass spectrometry. 5 lines changed; the page grew by 732 bytes.

Revision 1 — 02:39, 30 Jun 2024
ImportRecordIna (talk)
start article on the analytical method
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Revision 2 — 19:05, 30 Jun 2024
ShortageShona (talk)
close an unbalanced quotation mark
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10A purity determination by [[High-performance liquid chromatography|chromatography]] establishes that one species dominates a sample; it does not establish which species. These are separate questions and require separate determinations. A [[Certificate of analysis|certificate]] reporting purity but no identity leaves the more fundamental of the two unanswered.{{r|usp1503}}10A purity determination by [[High-performance liquid chromatography|chromatography]] establishes that one species dominates a sample; it does not establish which species. These are separate questions and require separate determinations. A [[Certificate of analysis|certificate]] reporting purity but no identity leaves the more fundamental of the two unanswered.{{r|usp1503}}
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+12== Ionisation and mass analysis ==
+13Electrospray disperses a solution into charged droplets in an electric field; solvent evaporates and ions are released into the gas phase. It is a soft technique — the molecule survives largely intact — which is why it suits peptides and proteins. Matrix-assisted laser desorption is the other common soft method and tends to produce singly charged ions.{{r|aebersold2003}}
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+15Mass analysers differ in resolution and in mass accuracy. A quadrupole gives unit resolution and is adequate for confirming a mass to within a dalton; time-of-flight and orbital-trap analysers give sufficient resolution to determine a mass to a few parts per million, which distinguishes species a quadrupole cannot.
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12== References ==17== References ==
13{{reflist}}18{{reflist}}