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Using CRISPR-Cas9 in human and mouse cells, genome-wide, targeted loss-of-function pooled screens have been studied that has provided information about the inactivated genomic loci and strategies that modulate transcriptional activities (Shalem et al., 2015)

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Presumably, the interaction between Arg240 and the carboxylate group of L -DOPA and L -tyrosine (which are most probably of ionic nature as the amide group is mainly charged at the investigated pH) is too strong, resulting in the amide-containing substrates (tyramine and dopamine) being held in place by Arg240

specifically investigated Sermorelin with GHRP-2 (plus an additional GHRP)