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Keep peptides in a dedicated container or section

The most vulnerable include: Methionine Cysteine Tryptophan Tyrosine Histidine Asparagine These amino acids are more likely to undergo: Oxidation Deamidation Structural rearrangement As their numbers increase, overall peptide stability usually decreases

This process steals away precious methyl groups

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Scientific investigations continue to examine its molecular structure, copper-binding behaviour and peptide chemistry using established laboratory techniques and analytical methods