Abstract
Powerful combinatorial peptide library methods allow the discovery of peptide leads from diverse libraries. A new platform based on tandem mass spectrometry peptide sequencing coupled with high-performance size-exclusion chromatography enables identification of high-affinity peptidic ligands from focused libraries.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 320-321 |
| Number of pages | 2 |
| Journal | Nature Chemical Biology |
| Volume | 15 |
| Issue number | 4 |
| DOIs | |
| State | Published - Apr 1 2019 |
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ASJC Scopus subject areas
- Molecular Biology
- Cell Biology
Cite this
Affinity selection and sequencing. / Lam, Kit.
In: Nature Chemical Biology, Vol. 15, No. 4, 01.04.2019, p. 320-321.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Affinity selection and sequencing
AU - Lam, Kit
PY - 2019/4/1
Y1 - 2019/4/1
N2 - Powerful combinatorial peptide library methods allow the discovery of peptide leads from diverse libraries. A new platform based on tandem mass spectrometry peptide sequencing coupled with high-performance size-exclusion chromatography enables identification of high-affinity peptidic ligands from focused libraries.
AB - Powerful combinatorial peptide library methods allow the discovery of peptide leads from diverse libraries. A new platform based on tandem mass spectrometry peptide sequencing coupled with high-performance size-exclusion chromatography enables identification of high-affinity peptidic ligands from focused libraries.
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U2 - 10.1038/s41589-019-0253-2
DO - 10.1038/s41589-019-0253-2
M3 - Article
VL - 15
SP - 320
EP - 321
JO - Nature Chemical Biology
JF - Nature Chemical Biology
SN - 1552-4450
IS - 4
ER -