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Biomolecular Chemistry

  • NOSE Takeru, Professor
  • SUYAMA Keitaro, Assistant Professor
  • † Faculty of Arts and Science
Our laboratory mainly studies three subjects that are focus areas in peptide and protein chemistry research. These are as follows: (1) structure-function relationship of elastin-derived peptides; (2) determination and discovery of receptor-binding molecules, in particular, risk assessment of endocrine disruptors using a combination of computational and biochemical techniques; and (3) rational molecular design of enzyme inhibitors.

1. Structure–function relationship of elastin-derived peptides

The new dimeric peptides showed significantly high coacervation ability compared to known elastin-derived peptide analogs.

Elastin, a core protein of elastic fibers, exhibits coacervation. Coacervation is promoted by molecular interactions and shows temperature-dependent reversible association/dissociation under physiological conditions. Because of this unique characteristic, elastin and elastin-derived peptides have been considered to be useful as base materials for developing various biomedical products, skin substitutes, synthetic vascular grafts, and drug delivery systems. Although elastin-derived polypeptide (Val-Pro-Gly-Val-Gly)n has also been known to demonstrate coacervation properties, a sufficiently high (VPGVG)n repetition number (n > 40) is required for coacervation. In our recent studies, we newly developed a series of elastin-derived peptide dimers, (Cys-(Phe-Pro-Gly-Val-Gly)5)2 and (Cys-(Trp-Pro-Gly-Val-Gly)3)2, possessing a high coacervation potential. These novel dimeric peptides exhibited coacervation at significantly lower concentrations and temperatures than the commonly used elastin-derived peptide analogs; this result suggests that the coacervation ability of the peptides is enhanced by dimerization. On the basis of these findings, we are developing more potent elastin-derived peptide analogs with biological and chemical functions.

2. Determination and discovery of receptor-binding molecules

Plotting analysis for the ADDS method. ΔG vs. ΔΔG plotting analysis. The agonist/antagonist factor (ΔΔG) was calculated from the difference between average energies used by the agonist-bound receptor and antagonist-bound receptor, from each docking calculation. The size of each plot shows the relative molecular size of the test chemical.

We conducted risk assessment studies on endocrine disrupting chemicals (EDCs) by using a combination of computational and biochemical techniques. Nuclear receptors (NRs) are the main target of EDCs and play a central role as transcription factors in biological processes. Most of these NRs possess a ligand-binding domain (LBD) for binding a hormone or a hormone-like chemical. If chemicals that can bind to the LBD are identified, this information would, in turn, be very helpful for identifying chemicals that can bind to NRs. Such chemicals can be considered as dangerous EDCs that cause serious disruptions in the endocrine system. We established a novel screening method to study endocrine-disrupting chemicals by means of in silico docking calculations. We used the crystal structures of both agonist-bound LBDs and antagonist-bound LBDs as templates in the docking calculations, and estimated binding energies to discriminate between agonist and antagonist binding. This agonist/antagonist differential-docking screening (AADS) method did predict, for example, 4-(1-adamantyl)phenol as an agonist of the human estrogen receptor α. The AADS method is an approach that appears to predict both the binding ability and the agonist/antagonist function of chemicals for the target nuclear receptors.

3. Rational molecular design of enzyme inhibitors

The dipeptide inhibitor D-Leu-Phe-NHBzl (pF) inhibits chymotrypsin via a π-π stacking interaction between the Phe-phenyl group of the inhibitor and His57-imidazole ring at the active site of chymotrypsin. This π interaction is essential for inhibition. In this study, we considered whether the docking calculation based on the conventional molecular mechanics method was applicable to strengthening the inhibitory activity of the dipeptide inhibitor. On the basis of the calculations, we are going to design and synthesize tripeptide inhibitors and to perform in vitro enzyme-inhibition tests.

Crystal structure of the chymotrypsin and D-Leu-Phe-NHBzl(pF) complex (PDB:1AFQ).