Difference between revisions of "Part:BBa K4165143"
Line 5: | Line 5: | ||
Tau binding peptide targeting the PHF seed of Tau | Tau binding peptide targeting the PHF seed of Tau | ||
− | |||
===Usage and Biology=== | ===Usage and Biology=== | ||
− | + | KNT is a peptide tested as an inhibitor for tau aggregation. Its half maximal concentration for tau fibril formation inhibition is 182.8 μM, it can bind to tau at PHF seed (VQIVYK), its amino acid sequence is KNTPQHRKLRLS. It can penetrate cell membrane and cytosol of N2a cells | |
<!-- --> | <!-- --> | ||
<span class='h3bb'>Sequence and Features</span> | <span class='h3bb'>Sequence and Features</span> | ||
<partinfo>BBa_K4165143 SequenceAndFeatures</partinfo> | <partinfo>BBa_K4165143 SequenceAndFeatures</partinfo> | ||
+ | ===Reference=== | ||
+ | |||
+ | 1. Dammers, C., Yolcu, D., Kukuk, L., Willbold, D., Pickhardt, M., Mandelkow, E., ... & Funke, S. A. (2016). Selection and Characterization of Tau Binding ᴅ-Enantiomeric Peptides with Potential for Therapy of Alzheimer Disease. PLoS One, 11(12), e0167432. | ||
<!-- Uncomment this to enable Functional Parameter display | <!-- Uncomment this to enable Functional Parameter display |
Revision as of 18:10, 5 October 2022
KNT Peptide
Tau binding peptide targeting the PHF seed of Tau
Usage and Biology
KNT is a peptide tested as an inhibitor for tau aggregation. Its half maximal concentration for tau fibril formation inhibition is 182.8 μM, it can bind to tau at PHF seed (VQIVYK), its amino acid sequence is KNTPQHRKLRLS. It can penetrate cell membrane and cytosol of N2a cells Sequence and Features
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]
Reference
1. Dammers, C., Yolcu, D., Kukuk, L., Willbold, D., Pickhardt, M., Mandelkow, E., ... & Funke, S. A. (2016). Selection and Characterization of Tau Binding ᴅ-Enantiomeric Peptides with Potential for Therapy of Alzheimer Disease. PLoS One, 11(12), e0167432.