Abstract
Phenylketonuria (PKU) is known as a severe autosomal recessive disease caused by mutations in the expression enzyme, namely the PAH (Phenylalanine Hydroxylase) enzyme that causes the build-up of phenylalanine in the body. Untreated PKU affected brain damage and developmental problems. One of the strategies to reduce phenylalanine in the body is inhibiting B0AT1 activity using carotenoid and terpenoids compounds from Bok choy (Brassica rapa ssp.chinensis). In this study, we evaluated the nine carotenoid and terpenoid compounds from Bok choy as B0AT1 inhibitors. Nine Bok choy compounds, including alpha-carotene, beta-carotene, dimethylallyl pyrophosphate, isopentenyl pyrophosphate, lutein, neoxanthin, violaxanthin, geranylgeranyl diphosphate, and zeaxanthin were downloaded from PubChem database, while the 3D structure of B0AT1 was retrieved from Protein Data Bank RCSB. The compounds and B0AT1 were prepared by PyRx 0.8 version and Discovery Studio ver 21.1.1, then docked with Hex 8.0.0 and analyzed using Discovery Studio ver 21.1.1. This screening implies that three terpenoid compounds dimethylallyl pyrophosphate, isopentenyl pyrophosphate, and geranylgeranyl diphosphate interacts in C domain of B0AT1 while six carotenoid compounds, alpha carotene, beta-carotene, lutein, neoxanthin, violaxanthin, and zeaxanthin interacts in A domain and have possibility to inhibit B0AT1, because it interact with same A domain and have a stronger binding energy than phenylalanine. Alpha carotene has a same residue with phenylalanine, Phe144, making it potentially greater than other compound as inhibitors. Brassica rapa ssp. chinensis is indeed good for consumption by people with phenylketonuria, but it is also necessary to do a further compound screening in other low-phenylalanine diet foods to know which one is better as alternative phenylketonuria treatment.
Highlights
Phenylketonuria (PKU) is an inherited autosomal recessive congenital disease caused by a genetic mutation
PKU sufferers cannot break down the amino acid phenylalanine into tyrosine, the substance will accumulate in the body [2]
Interaction between Compounds and B0AT1 The interaction visualized in Figure 1 shows that three terpenoid group compounds bind to C domain of B0AT1, namely dimethylallyl pyrophosphate, isopentenyl pyrophosphate, and geranylgeranyl diphosphate, while compounds that bind to A domain of B0AT1 which is a transmembrane region are alpha carotene, betacarotene, lutein, neoxanthin, violaxanthin, and zeaxanthin, which are belong to the carotenoid group
Summary
Phenylketonuria (PKU) is an inherited autosomal recessive congenital disease caused by a genetic mutation. PKU sufferers cannot break down the amino acid phenylalanine into tyrosine, the substance will accumulate in the body [2]. B0AT1, known as SLC6A19, is a neutral amino acid transporter (AA0), which can be expressed in the intestine, especially in the jejunum [4]. Absorbed neutral amino acids consist of phenylalanine (Phe), leucin (Leu), methionine (Met), isoleucine (Ile), valine (Val), glycine (Gln), aspargine (Asn), cysteine (Cys), alanine (Ala), serin (Ser), threonine (Thr), glycine (Gly), tyrosine (Tyr), lysine (Lys), proline (Pro), tryptophan (Trp), and histidine (His). The presence of inhibition of B0AT1 shows a positive side for some cases of diseases such as restoring amino acid imbalances in phenylketonuria disease disorders [7]
Published Version (Free)
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have