Difference between revisions of "Part:BBa K2976006:Design"
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− | Synthetic construct | + | Synthetic construct, Chinese patent |
===References=== | ===References=== | ||
− | [1] Jie X.A PD-L1 targeting peptide and its application:CN201810650428.9[P].2018-11-20. | + | <p>[1] Jie X.A PD-L1 targeting peptide and its application:CN201810650428.9[P].2018-11-20.</p> |
− | [2] Hung ME, Leonard JN. Stabilization of exosome-targeting peptides via engineered glycosylation. J Biol Chem. 2015;290(13):8166-72 | + | <p>[2] Hung ME, Leonard JN. Stabilization of exosome-targeting peptides via engineered glycosylation. J Biol Chem. 2015;290(13):8166-72</p> |
Latest revision as of 02:07, 5 September 2019
Anti-PD-L1 peptide
Assembly Compatibility:
- 10COMPATIBLE WITH RFC[10]
- 12COMPATIBLE WITH RFC[12]
- 21COMPATIBLE WITH RFC[21]
- 23COMPATIBLE WITH RFC[23]
- 25COMPATIBLE WITH RFC[25]
- 1000COMPATIBLE WITH RFC[1000]
Design Notes
GNSTM should be fused to the N terminus of anti-PD-L1 peptide to enhance the stability. The amino acid sequence Asn-Ser-Thr (NST) is a standard N-linked glycosylation sequon, and the amino acids Ger and Met flanking sequon could increase glycosylation frequency in mammals.
Source
Synthetic construct, Chinese patent
References
[1] Jie X.A PD-L1 targeting peptide and its application:CN201810650428.9[P].2018-11-20.
[2] Hung ME, Leonard JN. Stabilization of exosome-targeting peptides via engineered glycosylation. J Biol Chem. 2015;290(13):8166-72