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. 1999 Aug;8(8):1571–1590. doi: 10.1110/ps.8.8.1571

The hydrogen exchange core and protein folding.

R Li 1, C Woodward 1
PMCID: PMC2144413  PMID: 10452602

Abstract

A database of hydrogen-deuterium exchange results has been compiled for proteins for which there are published rates of out-exchange in the native state, protection against exchange during folding, and out-exchange in partially folded forms. The question of whether the slow exchange core is the folding core (Woodward C, 1993, Trends Biochem Sci 18:359-360) is reexamined in a detailed comparison of the specific amide protons (NHs) and the elements of secondary structure on which they are located. For each pulsed exchange or competition experiment, probe NHs are shown explicitly; the large number and broad distribution of probe NHs support the validity of comparing out-exchange with pulsed-exchange/competition experiments. There is a strong tendency for the same elements of secondary structure to carry NHs most protected in the native state, NHs first protected during folding, and NHs most protected in partially folded species. There is not a one-to-one correspondence of individual NHs. Proteins for which there are published data for native state out-exchange and theta values are also reviewed. The elements of secondary structure containing the slowest exchanging NHs in native proteins tend to contain side chains with high theta values or be connected to a turn/loop with high theta values. A definition for a protein core is proposed, and the implications for protein folding are discussed. Apparently, during folding and in the native state, nonlocal interactions between core sequences are favored more than other possible nonlocal interactions. Other studies of partially folded bovine pancreatic trypsin inhibitor (Barbar E, Barany G, Woodward C, 1995, Biochemistry 34:11423-11434; Barber E, Hare M, Daragan V, Barany G, Woodward C, 1998, Biochemistry 37:7822-7833), suggest that developing cores have site-specific energy barriers between microstates, one disordered, and the other(s) more ordered.

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Selected References

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  1. Alonso D. O., Daggett V. Molecular dynamics simulations of protein unfolding and limited refolding: characterization of partially unfolded states of ubiquitin in 60% methanol and in water. J Mol Biol. 1995 Mar 31;247(3):501–520. doi: 10.1006/jmbi.1994.0156. [DOI] [PubMed] [Google Scholar]
  2. Arcus V. L., Vuilleumier S., Freund S. M., Bycroft M., Fersht A. R. A comparison of the pH, urea, and temperature-denatured states of barnase by heteronuclear NMR: implications for the initiation of protein folding. J Mol Biol. 1995 Nov 24;254(2):305–321. doi: 10.1006/jmbi.1995.0618. [DOI] [PubMed] [Google Scholar]
  3. Arrington C. B., Robertson A. D. Microsecond protein folding kinetics from native-state hydrogen exchange. Biochemistry. 1997 Jul 22;36(29):8686–8691. doi: 10.1021/bi970872m. [DOI] [PubMed] [Google Scholar]
  4. Arrington C. B., Teesch L. M., Robertson A. D. Defining protein ensembles with native-state NH exchange: kinetics of interconversion and cooperative units from combined NMR and MS analysis. J Mol Biol. 1999 Jan 22;285(3):1265–1275. doi: 10.1006/jmbi.1998.2338. [DOI] [PubMed] [Google Scholar]
  5. Bai Y., Karimi A., Dyson H. J., Wright P. E. Absence of a stable intermediate on the folding pathway of protein A. Protein Sci. 1997 Jul;6(7):1449–1457. doi: 10.1002/pro.5560060709. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Bai Y., Milne J. S., Mayne L., Englander S. W. Primary structure effects on peptide group hydrogen exchange. Proteins. 1993 Sep;17(1):75–86. doi: 10.1002/prot.340170110. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Barbar E., Hare M., Daragan V., Barany G., Woodward C. Dynamics of the conformational ensemble of partially folded bovine pancreatic trypsin inhibitor. Biochemistry. 1998 May 26;37(21):7822–7833. doi: 10.1021/bi973102j. [DOI] [PubMed] [Google Scholar]
  8. Bond C. J., Wong K. B., Clarke J., Fersht A. R., Daggett V. Characterization of residual structure in the thermally denatured state of barnase by simulation and experiment: description of the folding pathway. Proc Natl Acad Sci U S A. 1997 Dec 9;94(25):13409–13413. doi: 10.1073/pnas.94.25.13409. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Bowie J. U., Reidhaar-Olson J. F., Lim W. A., Sauer R. T. Deciphering the message in protein sequences: tolerance to amino acid substitutions. Science. 1990 Mar 16;247(4948):1306–1310. doi: 10.1126/science.2315699. [DOI] [PubMed] [Google Scholar]
  10. Briggs M. S., Roder H. Early hydrogen-bonding events in the folding reaction of ubiquitin. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2017–2021. doi: 10.1073/pnas.89.6.2017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Buck M., Radford S. E., Dobson C. M. A partially folded state of hen egg white lysozyme in trifluoroethanol: structural characterization and implications for protein folding. Biochemistry. 1993 Jan 19;32(2):669–678. doi: 10.1021/bi00053a036. [DOI] [PubMed] [Google Scholar]
  12. Buck M., Radford S. E., Dobson C. M. Amide hydrogen exchange in a highly denatured state. Hen egg-white lysozyme in urea. J Mol Biol. 1994 Apr 1;237(3):247–254. doi: 10.1006/jmbi.1994.1228. [DOI] [PubMed] [Google Scholar]
  13. Burton R. E., Huang G. S., Daugherty M. A., Calderone T. L., Oas T. G. The energy landscape of a fast-folding protein mapped by Ala-->Gly substitutions. Nat Struct Biol. 1997 Apr;4(4):305–310. doi: 10.1038/nsb0497-305. [DOI] [PubMed] [Google Scholar]
  14. Bycroft M., Matouschek A., Kellis J. T., Jr, Serrano L., Fersht A. R. Detection and characterization of a folding intermediate in barnase by NMR. Nature. 1990 Aug 2;346(6283):488–490. doi: 10.1038/346488a0. [DOI] [PubMed] [Google Scholar]
  15. Chamberlain A. K., Handel T. M., Marqusee S. Detection of rare partially folded molecules in equilibrium with the native conformation of RNaseH. Nat Struct Biol. 1996 Sep;3(9):782–787. doi: 10.1038/nsb0996-782. [DOI] [PubMed] [Google Scholar]
  16. Chung E. W., Nettleton E. J., Morgan C. J., Gross M., Miranker A., Radford S. E., Dobson C. M., Robinson C. V. Hydrogen exchange properties of proteins in native and denatured states monitored by mass spectrometry and NMR. Protein Sci. 1997 Jun;6(6):1316–1324. doi: 10.1002/pro.5560060620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Clarke J., Fersht A. R. An evaluation of the use of hydrogen exchange at equilibrium to probe intermediates on the protein folding pathway. Fold Des. 1996;1(4):243–254. doi: 10.1016/S1359-0278(96)00038-7. [DOI] [PubMed] [Google Scholar]
  18. Clarke J., Itzhaki L. S., Fersht A. R. Hydrogen exchange at equilibrium: a short cut for analysing protein-folding pathways? Trends Biochem Sci. 1997 Aug;22(8):284–287. doi: 10.1016/s0968-0004(97)01087-6. [DOI] [PubMed] [Google Scholar]
  19. Dabora J. M., Pelton J. G., Marqusee S. Structure of the acid state of Escherichia coli ribonuclease HI. Biochemistry. 1996 Sep 17;35(37):11951–11958. doi: 10.1021/bi9611671. [DOI] [PubMed] [Google Scholar]
  20. Daggett V., Li A., Itzhaki L. S., Otzen D. E., Fersht A. R. Structure of the transition state for folding of a protein derived from experiment and simulation. J Mol Biol. 1996 Mar 29;257(2):430–440. doi: 10.1006/jmbi.1996.0173. [DOI] [PubMed] [Google Scholar]
  21. Deng Y., Smith D. L. Identification of unfolding domains in large proteins by their unfolding rates. Biochemistry. 1998 May 5;37(18):6256–6262. doi: 10.1021/bi972711o. [DOI] [PubMed] [Google Scholar]
  22. Dill K. A., Chan H. S. From Levinthal to pathways to funnels. Nat Struct Biol. 1997 Jan;4(1):10–19. doi: 10.1038/nsb0197-10. [DOI] [PubMed] [Google Scholar]
  23. Driscoll P. C., Gronenborn A. M., Wingfield P. T., Clore G. M. Determination of the secondary structure and molecular topology of interleukin-1 beta by use of two- and three-dimensional heteronuclear 15N-1H NMR spectroscopy. Biochemistry. 1990 May 15;29(19):4668–4682. doi: 10.1021/bi00471a023. [DOI] [PubMed] [Google Scholar]
  24. Elöve G. A., Bhuyan A. K., Roder H. Kinetic mechanism of cytochrome c folding: involvement of the heme and its ligands. Biochemistry. 1994 Jun 7;33(22):6925–6935. doi: 10.1021/bi00188a023. [DOI] [PubMed] [Google Scholar]
  25. Englander S. W., Kallenbach N. R. Hydrogen exchange and structural dynamics of proteins and nucleic acids. Q Rev Biophys. 1983 Nov;16(4):521–655. doi: 10.1017/s0033583500005217. [DOI] [PubMed] [Google Scholar]
  26. Englander S. W., Mayne L. Protein folding studied using hydrogen-exchange labeling and two-dimensional NMR. Annu Rev Biophys Biomol Struct. 1992;21:243–265. doi: 10.1146/annurev.bb.21.060192.001331. [DOI] [PubMed] [Google Scholar]
  27. Englander S. W. Native-state HX. Trends Biochem Sci. 1998 Oct;23(10):378–381. doi: 10.1016/s0968-0004(98)01281-x. [DOI] [PubMed] [Google Scholar]
  28. Fan P., Bracken C., Baum J. Structural characterization of monellin in the alcohol-denatured state by NMR: evidence for beta-sheet to alpha-helix conversion. Biochemistry. 1993 Feb 16;32(6):1573–1582. doi: 10.1021/bi00057a023. [DOI] [PubMed] [Google Scholar]
  29. Fersht A. R., Matouschek A., Serrano L. The folding of an enzyme. I. Theory of protein engineering analysis of stability and pathway of protein folding. J Mol Biol. 1992 Apr 5;224(3):771–782. doi: 10.1016/0022-2836(92)90561-w. [DOI] [PubMed] [Google Scholar]
  30. Fersht A. R. The sixth Datta Lecture. Protein folding and stability: the pathway of folding of barnase. FEBS Lett. 1993 Jun 28;325(1-2):5–16. doi: 10.1016/0014-5793(93)81405-o. [DOI] [PubMed] [Google Scholar]
  31. Freund C., Gehrig P., Holak T. A., Plückthun A. Comparison of the amide proton exchange behavior of the rapidly formed folding intermediate and the native state of an antibody scFv fragment. FEBS Lett. 1997 Apr 21;407(1):42–46. doi: 10.1016/s0014-5793(97)00306-2. [DOI] [PubMed] [Google Scholar]
  32. Freund C., Honegger A., Hunziker P., Holak T. A., Plückthun A. Folding nuclei of the scFv fragment of an antibody. Biochemistry. 1996 Jun 25;35(25):8457–8464. doi: 10.1021/bi952764a. [DOI] [PubMed] [Google Scholar]
  33. Gassner N. C., Baase W. A., Matthews B. W. A test of the "jigsaw puzzle" model for protein folding by multiple methionine substitutions within the core of T4 lysozyme. Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12155–12158. doi: 10.1073/pnas.93.22.12155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  34. Gladwin S. T., Evans P. A. Structure of very early protein folding intermediates: new insights through a variant of hydrogen exchange labelling. Fold Des. 1996;1(6):407–417. doi: 10.1016/S1359-0278(96)00057-0. [DOI] [PubMed] [Google Scholar]
  35. Grantcharova V. P., Baker D. Folding dynamics of the src SH3 domain. Biochemistry. 1997 Dec 16;36(50):15685–15692. doi: 10.1021/bi971786p. [DOI] [PubMed] [Google Scholar]
  36. Grantcharova V. P., Riddle D. S., Santiago J. V., Baker D. Important role of hydrogen bonds in the structurally polarized transition state for folding of the src SH3 domain. Nat Struct Biol. 1998 Aug;5(8):714–720. doi: 10.1038/1412. [DOI] [PubMed] [Google Scholar]
  37. Gregory R. B., Dinh A., Rosenberg A. The effect of tri-N-acetylglucosamine on hydrogen exchange in hen egg white lysozyme. J Biol Chem. 1986 Oct 25;261(30):13963–13968. [PubMed] [Google Scholar]
  38. Gu H., Kim D., Baker D. Contrasting roles for symmetrically disposed beta-turns in the folding of a small protein. J Mol Biol. 1997 Dec 12;274(4):588–596. doi: 10.1006/jmbi.1997.1374. [DOI] [PubMed] [Google Scholar]
  39. Hamada D., Goto Y. The equilibrium intermediate of beta-lactoglobulin with non-native alpha-helical structure. J Mol Biol. 1997 Jun 20;269(4):479–487. doi: 10.1006/jmbi.1997.1055. [DOI] [PubMed] [Google Scholar]
  40. Harding M. M., Williams D. H., Woolfson D. N. Characterization of a partially denatured state of a protein by two-dimensional NMR: reduction of the hydrophobic interactions in ubiquitin. Biochemistry. 1991 Mar 26;30(12):3120–3128. doi: 10.1021/bi00226a020. [DOI] [PubMed] [Google Scholar]
  41. Hilser V. J., Dowdy D., Oas T. G., Freire E. The structural distribution of cooperative interactions in proteins: analysis of the native state ensemble. Proc Natl Acad Sci U S A. 1998 Aug 18;95(17):9903–9908. doi: 10.1073/pnas.95.17.9903. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Hilton B. D., Trudeau K., Woodward C. K. Hydrogen exchange rates in pancreatic trypsin inhibitor are not correlated to thermal stability in urea. Biochemistry. 1981 Aug 4;20(16):4697–4703. doi: 10.1021/bi00519a027. [DOI] [PubMed] [Google Scholar]
  43. Holm L., Sander C. Touring protein fold space with Dali/FSSP. Nucleic Acids Res. 1998 Jan 1;26(1):316–319. doi: 10.1093/nar/26.1.316. [DOI] [PMC free article] [PubMed] [Google Scholar]
  44. Hughson F. M., Wright P. E., Baldwin R. L. Structural characterization of a partly folded apomyoglobin intermediate. Science. 1990 Sep 28;249(4976):1544–1548. doi: 10.1126/science.2218495. [DOI] [PubMed] [Google Scholar]
  45. Hvidt A., Nielsen S. O. Hydrogen exchange in proteins. Adv Protein Chem. 1966;21:287–386. doi: 10.1016/s0065-3233(08)60129-1. [DOI] [PubMed] [Google Scholar]
  46. Itzhaki L. S., Neira J. L., Fersht A. R. Hydrogen exchange in chymotrypsin inhibitor 2 probed by denaturants and temperature. J Mol Biol. 1997 Jul 4;270(1):89–98. doi: 10.1006/jmbi.1997.1049. [DOI] [PubMed] [Google Scholar]
  47. Itzhaki L. S., Otzen D. E., Fersht A. R. The structure of the transition state for folding of chymotrypsin inhibitor 2 analysed by protein engineering methods: evidence for a nucleation-condensation mechanism for protein folding. J Mol Biol. 1995 Nov 24;254(2):260–288. doi: 10.1006/jmbi.1995.0616. [DOI] [PubMed] [Google Scholar]
  48. Jackson S. E., elMasry N., Fersht A. R. Structure of the hydrophobic core in the transition state for folding of chymotrypsin inhibitor 2: a critical test of the protein engineering method of analysis. Biochemistry. 1993 Oct 26;32(42):11270–11278. doi: 10.1021/bi00093a002. [DOI] [PubMed] [Google Scholar]
  49. Jacobs M. D., Fox R. O. Staphylococcal nuclease folding intermediate characterized by hydrogen exchange and NMR spectroscopy. Proc Natl Acad Sci U S A. 1994 Jan 18;91(2):449–453. doi: 10.1073/pnas.91.2.449. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Jeng M. F., Englander S. W., Elöve G. A., Wand A. J., Roder H. Structural description of acid-denatured cytochrome c by hydrogen exchange and 2D NMR. Biochemistry. 1990 Nov 20;29(46):10433–10437. doi: 10.1021/bi00498a001. [DOI] [PubMed] [Google Scholar]
  51. Jennings P. A., Wright P. E. Formation of a molten globule intermediate early in the kinetic folding pathway of apomyoglobin. Science. 1993 Nov 5;262(5135):892–896. doi: 10.1126/science.8235610. [DOI] [PubMed] [Google Scholar]
  52. Karplus M. The Levinthal paradox: yesterday and today. Fold Des. 1997;2(4):S69–S75. doi: 10.1016/s1359-0278(97)00067-9. [DOI] [PubMed] [Google Scholar]
  53. Kim K. S., Fuchs J. A., Woodward C. K. Hydrogen exchange identifies native-state motional domains important in protein folding. Biochemistry. 1993 Sep 21;32(37):9600–9608. doi: 10.1021/bi00088a012. [DOI] [PubMed] [Google Scholar]
  54. Kim K. S., Woodward C. Protein internal flexibility and global stability: effect of urea on hydrogen exchange rates of bovine pancreatic trypsin inhibitor. Biochemistry. 1993 Sep 21;32(37):9609–9613. doi: 10.1021/bi00088a013. [DOI] [PubMed] [Google Scholar]
  55. Kuszewski J., Clore G. M., Gronenborn A. M. Fast folding of a prototypic polypeptide: the immunoglobulin binding domain of streptococcal protein G. Protein Sci. 1994 Nov;3(11):1945–1952. doi: 10.1002/pro.5560031106. [DOI] [PMC free article] [PubMed] [Google Scholar]
  56. Kuwajima K. The molten globule state as a clue for understanding the folding and cooperativity of globular-protein structure. Proteins. 1989;6(2):87–103. doi: 10.1002/prot.340060202. [DOI] [PubMed] [Google Scholar]
  57. Kuwajima K. The molten globule state of alpha-lactalbumin. FASEB J. 1996 Jan;10(1):102–109. doi: 10.1096/fasebj.10.1.8566530. [DOI] [PubMed] [Google Scholar]
  58. Lacroix E., Bruix M., López-Hernández E., Serrano L., Rico M. Amide hydrogen exchange and internal dynamics in the chemotactic protein CheY from Escherichia coli. J Mol Biol. 1997 Aug 22;271(3):472–487. doi: 10.1006/jmbi.1997.1178. [DOI] [PubMed] [Google Scholar]
  59. Lazaridis T., Karplus M. "New view" of protein folding reconciled with the old through multiple unfolding simulations. Science. 1997 Dec 12;278(5345):1928–1931. doi: 10.1126/science.278.5345.1928. [DOI] [PubMed] [Google Scholar]
  60. Loh S. N., Kay M. S., Baldwin R. L. Structure and stability of a second molten globule intermediate in the apomyoglobin folding pathway. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5446–5450. doi: 10.1073/pnas.92.12.5446. [DOI] [PMC free article] [PubMed] [Google Scholar]
  61. Loh S. N., Prehoda K. E., Wang J., Markley J. L. Hydrogen exchange in unligated and ligated staphylococcal nuclease. Biochemistry. 1993 Oct 19;32(41):11022–11028. doi: 10.1021/bi00092a011. [DOI] [PubMed] [Google Scholar]
  62. Lopez-Hernandez E, Serrano L. Structure of the transition state for folding of the 129 aa protein CheY resembles that of a smaller protein, CI-2. Fold Des. 1995;1(1):43–55. [PubMed] [Google Scholar]
  63. Lu J., Dahlquist F. W. Detection and characterization of an early folding intermediate of T4 lysozyme using pulsed hydrogen exchange and two-dimensional NMR. Biochemistry. 1992 May 26;31(20):4749–4756. doi: 10.1021/bi00135a002. [DOI] [PubMed] [Google Scholar]
  64. Lumry R. On the interpretation of data from isothermal processes. Methods Enzymol. 1995;259:628–720. doi: 10.1016/0076-6879(95)59065-x. [DOI] [PubMed] [Google Scholar]
  65. Matagne A., Chung E. W., Ball L. J., Radford S. E., Robinson C. V., Dobson C. M. The origin of the alpha-domain intermediate in the folding of hen lysozyme. J Mol Biol. 1998 Apr 17;277(5):997–1005. doi: 10.1006/jmbi.1998.1657. [DOI] [PubMed] [Google Scholar]
  66. Matouschek A., Serrano L., Meiering E. M., Bycroft M., Fersht A. R. The folding of an enzyme. V. H/2H exchange-nuclear magnetic resonance studies on the folding pathway of barnase: complementarity to and agreement with protein engineering studies. J Mol Biol. 1992 Apr 5;224(3):837–845. doi: 10.1016/0022-2836(92)90565-2. [DOI] [PubMed] [Google Scholar]
  67. Miller D. W., Dill K. A. A statistical mechanical model for hydrogen exchange in globular proteins. Protein Sci. 1995 Sep;4(9):1860–1873. doi: 10.1002/pro.5560040921. [DOI] [PMC free article] [PubMed] [Google Scholar]
  68. Miranker A., Radford S. E., Karplus M., Dobson C. M. Demonstration by NMR of folding domains in lysozyme. Nature. 1991 Feb 14;349(6310):633–636. doi: 10.1038/349633a0. [DOI] [PubMed] [Google Scholar]
  69. Montelione G. T., Anderson S. Structural genomics: keystone for a Human Proteome Project. Nat Struct Biol. 1999 Jan;6(1):11–12. doi: 10.1038/4878. [DOI] [PubMed] [Google Scholar]
  70. Mori S., van Zijl P. C., Shortle D. Measurement of water-amide proton exchange rates in the denatured state of staphylococcal nuclease by a magnetization transfer technique. Proteins. 1997 Jul;28(3):325–332. [PubMed] [Google Scholar]
  71. Morozova-Roche L. A., Arico-Muendel C. C., Haynie D. T., Emelyanenko V. I., Van Dael H., Dobson C. M. Structural characterisation and comparison of the native and A-states of equine lysozyme. J Mol Biol. 1997 May 23;268(5):903–921. doi: 10.1006/jmbi.1997.0996. [DOI] [PubMed] [Google Scholar]
  72. Morozova L. A., Haynie D. T., Arico-Muendel C., Van Dael H., Dobson C. M. Structural basis of the stability of a lysozyme molten globule. Nat Struct Biol. 1995 Oct;2(10):871–875. doi: 10.1038/nsb1095-871. [DOI] [PubMed] [Google Scholar]
  73. Mullins L. S., Pace C. N., Raushel F. M. Conformational stability of ribonuclease T1 determined by hydrogen-deuterium exchange. Protein Sci. 1997 Jul;6(7):1387–1395. doi: 10.1002/pro.5560060702. [DOI] [PMC free article] [PubMed] [Google Scholar]
  74. Mullins L. S., Pace C. N., Raushel F. M. Investigation of ribonuclease T1 folding intermediates by hydrogen-deuterium amide exchange-two-dimensional NMR spectroscopy. Biochemistry. 1993 Jun 22;32(24):6152–6156. doi: 10.1021/bi00075a006. [DOI] [PubMed] [Google Scholar]
  75. Nash D. P., Jonas J. Structure of pressure-assisted cold denatured lysozyme and comparison with lysozyme folding intermediates. Biochemistry. 1997 Nov 25;36(47):14375–14383. doi: 10.1021/bi970881v. [DOI] [PubMed] [Google Scholar]
  76. Nash D., Lee B. S., Jonas J. Hydrogen-exchange kinetics in the cold denatured state of ribonuclease A. Biochim Biophys Acta. 1996 Sep 13;1297(1):40–48. doi: 10.1016/0167-4838(96)00085-4. [DOI] [PubMed] [Google Scholar]
  77. Neira J. L., Itzhaki L. S., Otzen D. E., Davis B., Fersht A. R. Hydrogen exchange in chymotrypsin inhibitor 2 probed by mutagenesis. J Mol Biol. 1997 Jul 4;270(1):99–110. doi: 10.1006/jmbi.1997.1088. [DOI] [PubMed] [Google Scholar]
  78. Onuchic J. N., Luthey-Schulten Z., Wolynes P. G. Theory of protein folding: the energy landscape perspective. Annu Rev Phys Chem. 1997;48:545–600. doi: 10.1146/annurev.physchem.48.1.545. [DOI] [PubMed] [Google Scholar]
  79. Orban J., Alexander P., Bryan P., Khare D. Assessment of stability differences in the protein G B1 and B2 domains from hydrogen-deuterium exchange: comparison with calorimetric data. Biochemistry. 1995 Nov 21;34(46):15291–15300. doi: 10.1021/bi00046a038. [DOI] [PubMed] [Google Scholar]
  80. Pan H., Barbar E., Barany G., Woodward C. Extensive nonrandom structure in reduced and unfolded bovine pancreatic trypsin inhibitor. Biochemistry. 1995 Oct 31;34(43):13974–13981. doi: 10.1021/bi00043a002. [DOI] [PubMed] [Google Scholar]
  81. Pan Y., Briggs M. S. Hydrogen exchange in native and alcohol forms of ubiquitin. Biochemistry. 1992 Nov 24;31(46):11405–11412. doi: 10.1021/bi00161a019. [DOI] [PubMed] [Google Scholar]
  82. Perrett S., Clarke J., Hounslow A. M., Fersht A. R. Relationship between equilibrium amide proton exchange behavior and the folding pathway of barnase. Biochemistry. 1995 Jul 25;34(29):9288–9298. doi: 10.1021/bi00029a003. [DOI] [PubMed] [Google Scholar]
  83. Radford S. E., Buck M., Topping K. D., Dobson C. M., Evans P. A. Hydrogen exchange in native and denatured states of hen egg-white lysozyme. Proteins. 1992 Oct;14(2):237–248. doi: 10.1002/prot.340140210. [DOI] [PubMed] [Google Scholar]
  84. Radford S. E., Dobson C. M., Evans P. A. The folding of hen lysozyme involves partially structured intermediates and multiple pathways. Nature. 1992 Jul 23;358(6384):302–307. doi: 10.1038/358302a0. [DOI] [PubMed] [Google Scholar]
  85. Raschke T. M., Marqusee S. The kinetic folding intermediate of ribonuclease H resembles the acid molten globule and partially unfolded molecules detected under native conditions. Nat Struct Biol. 1997 Apr;4(4):298–304. doi: 10.1038/nsb0497-298. [DOI] [PubMed] [Google Scholar]
  86. Robertson A. D., Baldwin R. L. Hydrogen exchange in thermally denatured ribonuclease A. Biochemistry. 1991 Oct 15;30(41):9907–9914. doi: 10.1021/bi00105a014. [DOI] [PubMed] [Google Scholar]
  87. Roder H., Elöve G. A., Englander S. W. Structural characterization of folding intermediates in cytochrome c by H-exchange labelling and proton NMR. Nature. 1988 Oct 20;335(6192):700–704. doi: 10.1038/335700a0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  88. Roder H., Wüthrich K. Protein folding kinetics by combined use of rapid mixing techniques and NMR observation of individual amide protons. Proteins. 1986 Sep;1(1):34–42. doi: 10.1002/prot.340010107. [DOI] [PubMed] [Google Scholar]
  89. Rosenberg A., Chakravarti K. Studies of hydrogen exchange in proteins. I. The exchange kinetics of bovine carbonic anhydrase. J Biol Chem. 1968 Oct 10;243(19):5193–5201. [PubMed] [Google Scholar]
  90. Schulman B. A., Redfield C., Peng Z. Y., Dobson C. M., Kim P. S. Different subdomains are most protected from hydrogen exchange in the molten globule and native states of human alpha-lactalbumin. J Mol Biol. 1995 Nov 10;253(5):651–657. doi: 10.1006/jmbi.1995.0579. [DOI] [PubMed] [Google Scholar]
  91. Schönbrunner N., Wey J., Engels J., Georg H., Kiefhaber T. Native-like beta-structure in a trifluoroethanol-induced partially folded state of the all-beta-sheet protein tendamistat. J Mol Biol. 1996 Jul 19;260(3):432–445. doi: 10.1006/jmbi.1996.0412. [DOI] [PubMed] [Google Scholar]
  92. Serrano L., Matouschek A., Fersht A. R. The folding of an enzyme. III. Structure of the transition state for unfolding of barnase analysed by a protein engineering procedure. J Mol Biol. 1992 Apr 5;224(3):805–818. doi: 10.1016/0022-2836(92)90563-y. [DOI] [PubMed] [Google Scholar]
  93. Shoemaker B. A., Wang J., Wolynes P. G. Structural correlations in protein folding funnels. Proc Natl Acad Sci U S A. 1997 Feb 4;94(3):777–782. doi: 10.1073/pnas.94.3.777. [DOI] [PMC free article] [PubMed] [Google Scholar]
  94. Sivaraman T., Kumar T. K., Chang D. K., Lin W. Y., Yu C. Events in the kinetic folding pathway of a small, all beta-sheet protein. J Biol Chem. 1998 Apr 24;273(17):10181–10189. doi: 10.1074/jbc.273.17.10181. [DOI] [PubMed] [Google Scholar]
  95. Smith D. L., Deng Y., Zhang Z. Probing the non-covalent structure of proteins by amide hydrogen exchange and mass spectrometry. J Mass Spectrom. 1997 Feb;32(2):135–146. doi: 10.1002/(SICI)1096-9888(199702)32:2<135::AID-JMS486>3.0.CO;2-M. [DOI] [PubMed] [Google Scholar]
  96. Sosnick T. R., Mayne L., Hiller R., Englander S. W. The barriers in protein folding. Nat Struct Biol. 1994 Mar;1(3):149–156. doi: 10.1038/nsb0394-149. [DOI] [PubMed] [Google Scholar]
  97. Stockman B. J., Euvrard A., Scahill T. A. Heteronuclear three-dimensional NMR spectroscopy of a partially denatured protein: the A-state of human ubiquitin. J Biomol NMR. 1993 May;3(3):285–296. doi: 10.1007/BF00212515. [DOI] [PubMed] [Google Scholar]
  98. Swint-Kruse L., Robertson A. D. Temperature and pH dependences of hydrogen exchange and global stability for ovomucoid third domain. Biochemistry. 1996 Jan 9;35(1):171–180. doi: 10.1021/bi9517603. [DOI] [PubMed] [Google Scholar]
  99. Tirado-Rives J., Orozco M., Jorgensen W. L. Molecular dynamics simulations of the unfolding of barnase in water and 8 M aqueous urea. Biochemistry. 1997 Jun 17;36(24):7313–7329. doi: 10.1021/bi970096i. [DOI] [PubMed] [Google Scholar]
  100. Tüchsen E., Woodward C. Hydrogen kinetics of peptide amide protons at the bovine pancreatic trypsin inhibitor protein-solvent interface. J Mol Biol. 1985 Sep 20;185(2):405–419. doi: 10.1016/0022-2836(85)90412-7. [DOI] [PubMed] [Google Scholar]
  101. Udgaonkar J. B., Baldwin R. L. Early folding intermediate of ribonuclease A. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8197–8201. doi: 10.1073/pnas.87.21.8197. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Varley P., Gronenborn A. M., Christensen H., Wingfield P. T., Pain R. H., Clore G. M. Kinetics of folding of the all-beta sheet protein interleukin-1 beta. Science. 1993 May 21;260(5111):1110–1113. doi: 10.1126/science.8493553. [DOI] [PubMed] [Google Scholar]
  103. Walsh S. T., Cheng H., Bryson J. W., Roder H., DeGrado W. F. Solution structure and dynamics of a de novo designed three-helix bundle protein. Proc Natl Acad Sci U S A. 1999 May 11;96(10):5486–5491. doi: 10.1073/pnas.96.10.5486. [DOI] [PMC free article] [PubMed] [Google Scholar]
  104. Wang A., Robertson A. D., Bolen D. W. Effects of a naturally occurring compatible osmolyte on the internal dynamics of ribonuclease A. Biochemistry. 1995 Nov 21;34(46):15096–15104. doi: 10.1021/bi00046a016. [DOI] [PubMed] [Google Scholar]
  105. Wang Q. W., Kline A. D., Wüthrich K. Amide proton exchange in the alpha-amylase polypeptide inhibitor Tendamistat studied by two-dimensional 1H nuclear magnetic resonance. Biochemistry. 1987 Oct 6;26(20):6488–6493. doi: 10.1021/bi00394a030. [DOI] [PubMed] [Google Scholar]
  106. Woodward C. K., Hilton B. D. Hydrogen isotope exchange kinetics of single protons in bovine pancreatic trypsin inhibitor. Biophys J. 1980 Oct;32(1):561–575. doi: 10.1016/S0006-3495(80)84990-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  107. Woodward C. K., Rosenberg A. Studies of hydrogen exchange in proteins. V. The correlation of ribonuclease exchange kinetics with the temperature-induced transition. J Biol Chem. 1971 Jul 10;246(13):4105–4113. [PubMed] [Google Scholar]
  108. Woodward C. K., Rosenberg A. Studies of hydrogen exchange in proteins. VI. Urea effects on ribonuclease exchange kinetics leading to a general model for hydrogen exchange from folded proteins. J Biol Chem. 1971 Jul 10;246(13):4114–4121. [PubMed] [Google Scholar]
  109. Woodward C. Is the slow exchange core the protein folding core? Trends Biochem Sci. 1993 Oct;18(10):359–360. doi: 10.1016/0968-0004(93)90086-3. [DOI] [PubMed] [Google Scholar]
  110. Woodward C., Li R. The slow-exchange core and protein folding. Trends Biochem Sci. 1998 Oct;23(10):379–381. doi: 10.1016/s0968-0004(98)01282-1. [DOI] [PubMed] [Google Scholar]
  111. Woodward C., Simon I., Tüchsen E. Hydrogen exchange and the dynamic structure of proteins. Mol Cell Biochem. 1982 Oct 29;48(3):135–160. doi: 10.1007/BF00421225. [DOI] [PubMed] [Google Scholar]
  112. Yamasaki K., Ogasahara K., Yutani K., Oobatake M., Kanaya S. Folding pathway of Escherichia coli ribonuclease HI: a circular dichroism, fluorescence, and NMR study. Biochemistry. 1995 Dec 26;34(51):16552–16562. doi: 10.1021/bi00051a003. [DOI] [PubMed] [Google Scholar]
  113. Yi Q., Baker D. Direct evidence for a two-state protein unfolding transition from hydrogen-deuterium exchange, mass spectrometry, and NMR. Protein Sci. 1996 Jun;5(6):1060–1066. doi: 10.1002/pro.5560050608. [DOI] [PMC free article] [PubMed] [Google Scholar]
  114. Yi Q., Scalley M. L., Simons K. T., Gladwin S. T., Baker D. Characterization of the free energy spectrum of peptostreptococcal protein L. Fold Des. 1997;2(5):271–280. doi: 10.1016/S1359-0278(97)00038-2. [DOI] [PubMed] [Google Scholar]
  115. Yu H., Rosen M. K., Schreiber S. L. 1H and 15N assignments and secondary structure of the Src SH3 domain. FEBS Lett. 1993 Jun 7;324(1):87–92. doi: 10.1016/0014-5793(93)81538-b. [DOI] [PubMed] [Google Scholar]
  116. Zhang J., Peng X., Jonas A., Jonas J. NMR study of the cold, heat, and pressure unfolding of ribonuclease A. Biochemistry. 1995 Jul 11;34(27):8631–8641. doi: 10.1021/bi00027a012. [DOI] [PubMed] [Google Scholar]

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