[Solid phase reaction of hemoglobin with spillover hydrogen]
| Autor: | N. F. Myasoedov, Yu. A. Borisov, E. M. Dorokhova, A. K. Dadayan, V. S. Kozik, B. V. Vaskovsky, Yu. A. Zolotarev, R. Kh. Ziganshin |
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| Rok vydání: | 2009 |
| Předmět: |
Models
Molecular Hydrogen Protein subunit Inorganic chemistry chemistry.chemical_element Tritium Biochemistry Catalysis Hemoglobin complex Hemoglobins Enzymatic hydrolysis medicine Animals Trypsin Protein Structure Quaternary Chromatography Chemistry Organic Chemistry Protein Subunits Multiprotein Complexes Cattle Hemoglobin medicine.drug |
| Zdroj: | Bioorganicheskaia khimiia. 35(1) |
| ISSN: | 0132-3423 |
| Popis: | The reaction of high-temperature solid-state catalytic isotope exchange (HSCIE) between bovine hemoglobin and spillover hydrogen (SH) was studied. It was shown that, in the field of subunit contact, there is a significant decrease in ability for hydrogen exchange by SH. A comparison of the distribution of the isotope label in the hemoglobin alpha-subunit was carried out for the HSCIE reaction with the hemoglobin complex and with the free alpha-subunit. To this end, enzymatic hydrolysis of protein under the action of trypsin was carried out. The separation of tritium-labeled tryptic peptides was achieved by HPLC. Changes in availability of polypeptide chain fragments caused by complex formation were calculated using a molecular model. The formation of the protein complex was shown to lead to a decrease in the ability of fragments of alpha-subunits MFLSFPTTK (A(32-40)) and VDPVNFK (A(93-99)) for hydrogen replacement by tritium by almost an order of magnitude; hence, their availability to water (1.4 A) twice decreased on the average. The decrease in ability to an exchange of hydrogen by spillover tritium on the formation of hemoglobin complex was shown to be connected with a reduction in availability of polypeptide chain fragments participating in spatial interactions of subunits with each other. Thus, the HSCIE reaction can be used not only for the preparative obtaining of tritium-labeled compounds, but also for determining the contact area in the formation of protein complexes. |
| Databáze: | OpenAIRE |
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