Ferguson plot analysis of multiple intermediate species of thermally unfolded bovine serum albumin.


Journal

Biophysical chemistry
ISSN: 1873-4200
Titre abrégé: Biophys Chem
Pays: Netherlands
ID NLM: 0403171

Informations de publication

Date de publication:
10 2023
Historique:
received: 17 05 2023
revised: 28 07 2023
accepted: 14 08 2023
medline: 6 9 2023
pubmed: 24 8 2023
entrez: 23 8 2023
Statut: ppublish

Résumé

Ferguson plot was used to characterize the multiple intermediate species of bovine serum albumin (BSA) upon thermal unfolding. Differential scanning calorimetry showed an irreversible melting of BSA in Tris-HCl and phosphate buffers with a mid-transition temperature, Tm, of ∼68 °C. Thermally unfolded BSA was analyzed by agarose native gel electrophoresis stained by Coomassie blue and SYPRO Orange staining as a function of pH or protein concentration. SYPRO Orange was used to stain unfolded proteins. BSA heated at 70 and 80 °C, i.e., above the Tm, formed multiple intermediate species, which depended on the pH between 7.0 and 8.0, protein concentration and which buffer was used. These intermediate species were analyzed by Ferguson plot, which showed that BSA heated at 60 °C had a similar size to the native BSA, indicating that they are either native or native-like state consistent with no SYPRO Orange staining. The intermediate species observed at higher temperatures with the mobility less than that of the native BSA showed a steeper Ferguson plot and were stained by SYPRO Orange, indicating that these species had a larger hydrodynamic size than the native BSA and were unfolded.

Identifiants

pubmed: 37611350
pii: S0301-4622(23)00146-1
doi: 10.1016/j.bpc.2023.107095
pii:
doi:

Substances chimiques

Serum Albumin, Bovine 27432CM55Q

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

107095

Informations de copyright

Copyright © 2023 Elsevier B.V. All rights reserved.

Déclaration de conflit d'intérêts

Declaration of Competing Interest This work was supported by Kyokuto Pharmaceutical Industrial Co., Ltd. Y.T., M.N., and T.A. (Teruo Akuta) are employees of the for-profit company Kyokuto Pharmaceuticals. S·N and K.T. are staffs of University of Tokyo and have no conflict of interest. Tsutomu Arakawa used to belong to the for-profit company Alliance Protein Laboratories but currently has no conflict of interest.

Auteurs

Yui Tomioka (Y)

Research and Development Division, Kyokuto Pharmaceutical Industrial Co., Ltd., 3333-26, Aza-Asayama, Kamitezuna Takahagi-shi, Ibaraki 318-0004, Japan. Electronic address: y.tomioka@kyokutoseiyaku.co.jp.

Satoru Nagatoishi (S)

The Institute of Medical Sciences, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan. Electronic address: nagatoishi@bioeng.t.u-tokyo.ac.jp.

Masataka Nakagawa (M)

Research and Development Division, Kyokuto Pharmaceutical Industrial Co., Ltd., 3333-26, Aza-Asayama, Kamitezuna Takahagi-shi, Ibaraki 318-0004, Japan. Electronic address: m.nakagawa@kyokutoseiyaku.co.jp.

Kouhei Tsumoto (K)

The Institute of Medical Sciences, The University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan; School of Engineering, The University of Tokyo, 7-3-1, Hongo, Bunkyo-ku, Tokyo 113-8656, Japan. Electronic address: tsumoto@bioeng.t.u-tokyo.ac.jp.

Tsutomu Arakawa (T)

Alliance Protein Laboratories, 13380 Pantera Rd, San Diego, CA 92130, USA. Electronic address: tarakawa2@aol.com.

Teruo Akuta (T)

Research and Development Division, Kyokuto Pharmaceutical Industrial Co., Ltd., 3333-26, Aza-Asayama, Kamitezuna Takahagi-shi, Ibaraki 318-0004, Japan. Electronic address: t.akuta@kyokutoseiyaku.co.jp.

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