Journal article
Authors list: Hien, Le Thi; Schierling, B.; Ryazanova, A. Yu.; Zatsepin, T. S.; Volkov, E. M.; Kubareva, E. A.; Velichko, T. I.; Pingoud, A.; Oretskaya, T. S.
Publication year: 2009
Pages: 549-555
Journal: Russian Journal of Bioorganic Chemistry
Volume number: 35
Issue number: 5
ISSN: 1068-1620
eISSN: 1608-330X
DOI Link: https://doi.org/10.1134/S1068162009050033
Publisher: Springer
Abstract:
Derivatives of azobenzene which contained a maleimide group in one of the benzene rings (for binding to a protein cysteine residue) and maleimide, hydroxyl, or carboxyl substitutes in another benzene ring were synthesized. The reactivity of these compounds towards a cysteine residue of a protein and their optical properties in a free form and after their attachment to the mutant forms of the SsoII restriction endonuclease were studied.
Citation Styles
Harvard Citation style: Hien, L., Schierling, B., Ryazanova, A., Zatsepin, T., Volkov, E., Kubareva, E., et al. (2009) New azobenzene derivatives for directed modification of proteins, Russian Journal of Bioorganic Chemistry, 35(5), pp. 549-555. https://doi.org/10.1134/S1068162009050033
APA Citation style: Hien, L., Schierling, B., Ryazanova, A., Zatsepin, T., Volkov, E., Kubareva, E., Velichko, T., Pingoud, A., & Oretskaya, T. (2009). New azobenzene derivatives for directed modification of proteins. Russian Journal of Bioorganic Chemistry. 35(5), 549-555. https://doi.org/10.1134/S1068162009050033
Keywords
CONFORMATION; CROSS-LINKING; HELIX CONTENT; ION CHANNELS; maleimidoazobenzene; PHOTOCHEMICAL CONTROL; PHOTO-CONTROL; proteins, modification of cysteine residues; the SsoII restriction endonuclease
