In HEK-293 cells, the hMC3R mutations C115S and C162S in transmembrane domain 3 significantly decreased the binding affinity and potency of NDP-MSH.
In plain wordsIn cells, two changes in the MC3R receptor lowered how tightly and strongly the NDP-MSH peptide acted on it.
- Peptide
- Melanotan I (afamelanotide)
- Outcome
- DecreaseNDP-MSH binding affinity and potency at C115S and C162S hMC3R mutants
- Study
humann: not reported in source
HEK-293 cells expressing cysteine-to-serine hMC3R mutants- Outcome group
- Receptor activity and mechanism · Pharmacology
Source sentences
two other mutations C115S and C162S in TM3 significantly decreased NDP-MSH binding affinity and potency.
1 context sentence(design, population, supporting numbers)
We replaced these cysteines with serine and expressed these receptors in HEK-293 cells which lack endogenous MC3R.
In this study, Melanotan I (afamelanotide) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Melanotan I (afamelanotide).