The electrochemically induced conformational transition of disulfides in bovine serum albumin studied by thin layer circular dichroism spectroelectrochemistry Original Research Article

The conformational transition of disulfides in bovine serum albumin (BSA) induced by electrochemical redox reaction of disulfides were monitored by in-situ circular dichroism (CD) spectroelectrochemistry, with a long optical path thin layer cell and analyzed by a singular value decomposition least square (SVDLS) method. Electrochemical reduction of disulfides drives the left-handed conformation of disulfides changed into the right-handed. At open circuit, eight of the 17 disulfides were of left-handed conformation. Four of the 17 disulfides took part in the electrochemical reduction with an EC mechanism. Only one-fourth of the reduced disulfides returned to left-handed conformation in the re-oxidation process. Some parameters of the electrochemical reduction process, i.e. the number of electrons transferred and electron transfer coefficient, n=8, αn=0.15, apparent formal potential, E10′=−0.65(±0.01) V, standard heterogeneous electron transfer rate constant, k10=(2.84±0.14)×10−5 cm s−1 and chemical reaction equilibrium constant, Kc=(5.13±0.12)×10−2, were also obtained by double logarithmic analysis based on the near-UV absorption spectra with applied potentials.