Secondary structure and temperature behaviour of acetylcholinesterase
- 1 May 1993
- journal article
- Published by Wiley in European Journal of Biochemistry
- Vol. 213 (3), 1235-1242
- https://doi.org/10.1111/j.1432-1033.1993.tb17874.x
Abstract
The secondary structure of the acetylcholinesterase and its temperature behaviour have been investigated using Fourier-transform infrared (FTIR) spectroscopy. The data are compared to the structure obtained by X-ray analysis of the crystalline enzyme. The secondary structure was determined using the spectral features observed in the amide-I band (H2O buffer) and amide-I' band (D2O buffer) at 1600-1700 cm-1, taking advantage of resolution-enhancement techniques along with least-squares band-fitting procedures. The relative amounts of different secondary-structure elements, 34-36% for alpha-helices, 19-25% for beta-sheets, 15-16% for turns and 13-17% for irregular structures, were estimated. These data, obtained with the enzyme in solution, correlate well with X-ray data of the crystalline protein [Sussman, J. L., Hard, M., Frolow, F., Oefner, C., Goldman, A., Toker, L. & Silman, I. (1991) Science 253, 872-879]. These results are also in good agreement with those obtained by computing the psi and phi angles of the peptide backbone using the Kabsch and Sanders method [Kabsch, W. & Sanders, C. (1983) Biopolymers 22, 2577-2637]. In conjunction with the X-ray data, two bands in the FTIR spectra were assigned to different populations of long and short alpha-helices. Until now this phenomenon has only been described by theoretical calculations [Nevskaya, N. A. & Chirgadze, Yu. N. (1976) Biopolymers 15, 637-648]. The relationship between the thermally induced loss of enzyme activity and secondary-structure changes has also been investigated. The decrease in enzyme activity to zero at 30-40 degrees C was accompanied only by minor changes in the secondary structure. At 55-60 degrees C, denaturation of AChE occurs. In this temperature range, all bands assigned to the various secondary-structure elements abruptly disappear in a co-operative and irreversible manner, whereas the beta-aggregation bands (at 1622 cm-1 and the corresponding high-frequency band) increase in intensity at the same rate.Keywords
This publication has 44 references indexed in Scilit:
- Beware of proteins in DMSOBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1991
- An infrared spectroscopic study of β‐galactosidase structure in aqueous solutionsFEBS Letters, 1989
- Structural and conformational changes of β-lactoglobulin B: an infrared spectroscopic study of the effect of pH and temperatureBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1988
- The solution structure of concanavalin A probed by FT-IR spectroscopyBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1988
- New insight into protein secondary structure from resolution-enhanced infrared spectraBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1988
- Conformation similarities of the globular and tailed forms of acetylcholinesterase from Torpedo californiaBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1987
- Circular dichroism studies of acetylcholine sterase conformation. Comparison of the 11 S and 5.6 S species and the differences induced by inhibitory ligandsBiochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology, 1985
- Dictionary of protein secondary structure: Pattern recognition of hydrogen‐bonded and geometrical featuresBiopolymers, 1983
- Protein structure by Fourier transform infrared spectroscopy: Second derivative spectraBiochemical and Biophysical Research Communications, 1983
- The Infrared Spectra of Polypeptides in Various Conformations: Amide I and II Bands1Journal of the American Chemical Society, 1961