Researchers make breakthrough in antioxidant enzyme linked to jaundice
A Japanese research team involving Osaka University investigated biliverdin reductase, the enzyme producing bilirubin – a substance linked with jaundice – from biliverdin (BV). Two BV molecules were found at the enzyme reaction site, in an unusual stacked arrangement. Mutation experiments confirmed which enzyme amino acid was necessary for bilirubin production. In the proposed mechanism, this amino acid transfers hydrogen to one BV molecule, using the other BV as a conduit. This aids the search for anti-jaundice drugs.
Osaka – Jaundice, marked by yellowing of the skin, is common in infants, but also a symptom of various adult diseases. This discoloration is caused by excess bilirubin (BR), the substance that gives bile its yellow tinge. However, BR is also a vital antioxidant, which at healthy levels protects cells against peroxide damage. Its production in the body, though, has long been a source of uncertainty.
Now, a Japanese research collaboration involving Osaka University believes it has the answer. BR is already known to be produced from a related chemical, biliverdin (BV), by the enzyme biliverdin reductase (BVR). The enzyme wraps around BV and transfers two hydrogen atoms – one positive and one negative – to produce the yellow antioxidant. However, biologists could not establish which part of the enzyme was chemically involved in the process (the active site), or where the positive hydrogen came from. The findings were recently reported in Nature Communications.
"Previous studies used BVR from rats, and could never crystallize the enzyme well enough to determine how it binds to BV," study co-author Keiichi Fukuyama says. "We realized that the same enzyme in Synechocystis bacteria had an almost identical fold-shape, but was easier to examine by X-ray crystallography."
To their surprise, the researchers found two molecules of BV – one stacked upon the other – at the active site, even though only one is converted to BR. From the X-ray data, they deduced why two were needed. The first BV, because of the direction it faces to receive the negative hydrogen, cannot accept the positive hydrogen directly from the enzyme. Instead, the second BV acts as a hydrogen conduit to enable the process, but is not itself converted to BR.
From the structure, the researchers proposed which of the enzyme's 328 amino acids actually provides the positive hydrogen atom. Then, they performed experiments in which the enzymes were mutated to specifically remove that amino acid, while leaving the others intact. The resulting enzymes, whether from bacteria, rats, or humans, were virtually unable to produce BR. Further experiments confirmed that the rat and human enzymes also used two BV molecules, just like the bacteria.
"Such neat stacking of two substrate molecules during enzymatic processes is very rare," Fukuyama says. "A better understanding of BR production is not just exciting for biochemistry, but should help us develop drugs for diseases marked by severe jaundice from excess BR, such as hepatitis."
More information: Haruna Takao et al. A substrate-bound structure of cyanobacterial biliverdin reductase identifies stacked substrates as critical for activity, Nature Communications (2017). DOI: 10.1038/ncomms14397
Journal information: Nature Communications
Provided by Osaka University