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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Pegylated catalase as a potential alternative to treat vitiligo and UV induced skin damage

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Author(s):
Santos, Joao H. P. M. [1] ; Oliveira, Camila A. [1, 2] ; Rocha, Beatriz M. [1] ; Carretero, Gustavo [3] ; Rangel-Yagui, Carlota O. [1]
Total Authors: 5
Affiliation:
[1] Univ Sao Paulo, Dept Biochem & Pharmaceut Technol, Ave Prof Lineu Prestes 580 Bloco 16, BR-05508000 Sao Paulo, SP - Brazil
[2] Fundacao Oswaldo Cruz, Lab Dev & Analyt Validat Farmanguinhos, Rio De Janeiro, RJ - Brazil
[3] Univ Sao Paulo, Inst Chem, Dept Biochem, Sao Paulo, SP - Brazil
Total Affiliations: 3
Document type: Journal article
Source: Bioorganic & Medicinal Chemistry; v. 30, JAN 15 2021.
Web of Science Citations: 0
Abstract

The metabolic function of catalase (CAT) is to prevent oxidative damage to tissues through the hydrolysis of hydrogen peroxide, which is a strong oxidizing agent. It has been suggested as an alternative to treat skin diseases related to oxidative stress, such as vitiligo. Owing to the instability associated to the protein nature, topical use of CAT is challenging and, in this sense, PEGylation can be an interesting alternative. Here, we conjugated CAT to methoxy-poly(ethylene oxide) (mPEG) of 10, 20 and 40 kDa, by means of a nucleophilic attack of epsilon-amino groups to an electron-deficient carbonyl group of the reactive PEG, resulting in site specifically PEGylated bioconjugates. PEGylation yields ranged from 31% +/- 2% for CAT-PEG40 to 59% +/- 4% for CAT-PEG20 and were strongly affected by the reaction pH owing to the protonation/deprotonation state of primary amines of lysine and N-terminal residues. PEGylated conjugates were purified by size-exclusion chromatography (purity > 95%) and characterized by circular dichroism. Irrespectively of MW, PEG did not affected CAT secondary and tertiary structure, but a decrease in specific activity was observed, more pronounced when PEGs of higher MWs were used. However, this loss of activity is compensated by the increased long-term stability, with a gain of >5 times in t(1/2). In vitro antioxidant activity of CAT-PEG20 showed complete elimination of lipid peroxidation at the skin upper layer (stratum corneum) suitable for a topical use to treat vitiligo, as well as other skin conditions related to oxidative stress. (AU)

FAPESP's process: 16/22065-5 - N-terminal pegylation of proteins and purification by aqueous two-phase systems
Grantee:Carlota de Oliveira Rangel Yagui
Support type: Regular Research Grants