Abstract
Photoactivatable caged protons have been used to trigger proton transfer reactions in aqueous solutions of acetate, glutamate, and poly-L-glutamic acid, and the volumetric and enthalpic changes have been detected and characterized by means of time-resolved photoacoustics. Neutralization of carboxylates in aqueous solutions invariably results in an expansion of the solution due to the disappearance of two charges and is accompanied by little enthalpic change. The reactions occur with thermally activated, apparent bimolecular rates on the order of 10(10) M(-1)s(-1). In the case of aqueous solutions of poly-L-glutamic acid at pH around the pK(a) of the coil-to-helix transition, diffusional binding of a proton by carboxylates is followed by a sequential reaction with rate 1.06 (+/- 0.05) x 10(7)s(-1). This step is not thermally activated in the temperature range we have investigated and is likely related to local formation of hydrogen bonds near the protonation site. This structural event may constitute a rate-limiting step in helix propagation.
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- Abbruzzetti S., Crema E., Masino L., Vecli A., Viappiani C., Small J. R., Libertini L. J., Small E. W. Fast events in protein folding: structural volume changes accompanying the early events in the N-->I transition of apomyoglobin induced by ultrafast pH jump. Biophys J. 2000 Jan;78(1):405–415. doi: 10.1016/S0006-3495(00)76603-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ballew R. M., Sabelko J., Gruebele M. Direct observation of fast protein folding: the initial collapse of apomyoglobin. Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):5759–5764. doi: 10.1073/pnas.93.12.5759. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ballew R. M., Sabelko J., Gruebele M. Observation of distinct nanosecond and microsecond protein folding events. Nat Struct Biol. 1996 Nov;3(11):923–926. doi: 10.1038/nsb1196-923. [DOI] [PubMed] [Google Scholar]
- Callis J. B., Parson W. W., Gouterman M. Fast changes of enthalpy and volume on flash excitation of Chromatium chromatophores. Biochim Biophys Acta. 1972 May 25;267(2):348–362. doi: 10.1016/0005-2728(72)90122-3. [DOI] [PubMed] [Google Scholar]
- Chalikian T. V., Bresiauer K. J. On volume changes accompanying conformational transitions of biopolymers. Biopolymers. 1996 Nov;39(5):619–626. doi: 10.1002/(sici)1097-0282(199611)39:5<619::aid-bip1>3.0.co;2-z. [DOI] [PubMed] [Google Scholar]
- Chalikian T. V., Gindikin V. S., Breslauer K. J. Volumetric characterizations of the native, molten globule and unfolded states of cytochrome c at acidic pH. J Mol Biol. 1995 Jul 7;250(2):291–306. doi: 10.1006/jmbi.1995.0377. [DOI] [PubMed] [Google Scholar]
- Cocco M. J., Kao Y. H., Phillips A. T., Lecomte J. T. Structural comparison of apomyoglobin and metaquomyoglobin: pH titration of histidines by NMR spectroscopy. Biochemistry. 1992 Jul 21;31(28):6481–6491. doi: 10.1021/bi00143a018. [DOI] [PubMed] [Google Scholar]
- Creighton T. E. Protein folding. Biochem J. 1990 Aug 15;270(1):1–16. doi: 10.1042/bj2700001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gross M., Jaenicke R. Proteins under pressure. The influence of high hydrostatic pressure on structure, function and assembly of proteins and protein complexes. Eur J Biochem. 1994 Apr 15;221(2):617–630. doi: 10.1111/j.1432-1033.1994.tb18774.x. [DOI] [PubMed] [Google Scholar]
- Gruenewald B., Nicola C. U., Lustig A., Schwarz G., Klump H. Kinetics of the helix-coil transition of a polypeptide with non-ionic side groups, derived from ultrasonic relaxation measurements. Biophys Chem. 1979 Jan;9(2):137–147. doi: 10.1016/0301-4622(79)87008-8. [DOI] [PubMed] [Google Scholar]
- Hughson F. M., Barrick D., Baldwin R. L. Probing the stability of a partly folded apomyoglobin intermediate by site-directed mutagenesis. Biochemistry. 1991 Apr 30;30(17):4113–4118. doi: 10.1021/bi00231a001. [DOI] [PubMed] [Google Scholar]
- Kharakoz D. P. Volumetric properties of proteins and their analogs in diluted water solutions. 1. Partial volumes of amino acids at 15-55 degrees C. Biophys Chem. 1989 Oct;34(2):115–125. doi: 10.1016/0301-4622(89)80049-3. [DOI] [PubMed] [Google Scholar]
- Peters K. S., Snyder G. J. Time-resolved photoacoustic calorimetry: probing the energetics and dynamics of fast chemical and biochemical reactions. Science. 1988 Aug 26;241(4869):1053–1057. doi: 10.1126/science.3045967. [DOI] [PubMed] [Google Scholar]
- Small J. R. Deconvolution analysis for pulsed-laser photoacoustics. Methods Enzymol. 1992;210:505–521. doi: 10.1016/0076-6879(92)10026-a. [DOI] [PubMed] [Google Scholar]
- Small J. R., Libertini L. J., Small E. W. Analysis of photoacoustic waveforms using the nonlinear least squares method. Biophys Chem. 1992 Jan;42(1):29–48. doi: 10.1016/0301-4622(92)80005-p. [DOI] [PubMed] [Google Scholar]
- Thompson P. A., Eaton W. A., Hofrichter J. Laser temperature jump study of the helix<==>coil kinetics of an alanine peptide interpreted with a 'kinetic zipper' model. Biochemistry. 1997 Jul 29;36(30):9200–9210. doi: 10.1021/bi9704764. [DOI] [PubMed] [Google Scholar]
- Viappiani C., Abbruzzetti S., Small J. R., Libertini L. J., Small E. W. An experimental methodology for measuring volume changes in proton transfer reactions in aqueous solutions. Biophys Chem. 1998 Jul 13;73(1-2):13–22. doi: 10.1016/s0301-4622(98)00108-2. [DOI] [PubMed] [Google Scholar]
- Williams S., Causgrove T. P., Gilmanshin R., Fang K. S., Callender R. H., Woodruff W. H., Dyer R. B. Fast events in protein folding: helix melting and formation in a small peptide. Biochemistry. 1996 Jan 23;35(3):691–697. doi: 10.1021/bi952217p. [DOI] [PubMed] [Google Scholar]
