1. Academic Validation
  2. N-acetyl-L-methionine is a superior protectant of human serum albumin against post-translational oxidation as compared to N-acetyl-L-tryptophan

N-acetyl-L-methionine is a superior protectant of human serum albumin against post-translational oxidation as compared to N-acetyl-L-tryptophan

  • Biochem Biophys Rep. 2016 Apr 26:6:266-274. doi: 10.1016/j.bbrep.2016.04.011.
Yousuke Kouno 1 2 Makoto Anraku 1 3 Keishi Yamasaki 1 3 Yoshiro Okayama 2 Daisuke Iohara 1 Hedeaki Nakamura 4 Toru Maruyama 4 Fumitoshi Hirayama 1 3 Ulrich Kragh-Hansen 5 Masaki Otagiri 1 3
Affiliations

Affiliations

  • 1 Faculty of Pharmaceutical Sciences, Sojo University, Kumamoto 860-0082, Japan.
  • 2 Pharma Daiwa Yuge Pharmacy, Kumamoto City, Japan.
  • 3 DDS Research Institute, Sojo University, Kumamoto 860-0082, Japan.
  • 4 Graduate School of Pharmaceutical Sciences, Kumamoto University, Kumamoto 862-0973, Japan.
  • 5 Department of Biomedicine, University of Aarhus, DK-8000 Aarhus C, Denmark.
Abstract

Sodium octanoate and N-acetyl-L-tryptophan (N-AcTrp) are widely used as stabilizers during pasteurization and storage of albumin products. However, as compared with N-AcTrp, N-acetyl-L-methionine (N-AcMet) is superior in protecting albumin exposed to light during storage. Here, we examine, whether N-AcMet also is better than N-AcTrp to protect albumin against oxidation. Recombinant human serum albumin (rHSA) without and with N-AcMet or N-AcTrp was oxidized by using chloramine-T (CT) as a model compound for mimicking oxidative stress. Oxidation of rHSA was examined by determining carbonyl groups and advanced oxidation protein products. Structural changes were studied by native-PAGE, circular dichroism, intrinsic fluorescence and differential scanning calorimetry. The anti-oxidant capacity of CT-treated rHSA was quantified by its ability to scavenge peroxynitrite and the hydroxyl radical. The pharmacokinetics of indocyanine green-labeled albumin preparations was studied in male mice. We found that the number of chemical modifications and the structural changes of rHSA were significantly smaller in the presence of N-AcMet than in the presence of N-AcTrp. The anti-oxidant properties of CT-exposed rHSA were best protected by adding N-AcMet. Finally, N-AcMet is superior in preserving the normal pharmacokinetics of rHSA. Thus, N-AcMet is superior to N-AcTrp in protecting albumin preparations against oxidation. In addition, N-AcMet is probable also useful for protecting Other proteins. Therefore, N-AcMet should be useful as a new and effective stabilizer and antioxidant for albumin isolated from blood, rHSA, albumin-fusion proteins and for preparations of rHSA-therapeutic complexes.

Keywords

CD, circular dichroism; CT, chloramine-T; DSC, differential scanning calorimetry; HSA, human serum albumin; Human serum albumin; N-AcMet, N-acetyl-L-methionine; N-AcTrp, N-acetyl-L-tryptophan; N-Acetyl-L-Methionine; N-Acetyl-L-Tryptophan; Oct, octanoate; Oxidation; Pharmacokinetics; ROS, reactive oxygen species; Structural Changes; rHSA, recombinant HSA.

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