|
ABSTRACT
High-throughput, data-directed computational protocols for Structural Genomics (or Proteomics) are required in order to evaluate the protein products of genes for structure and function at rates comparable to current gene-sequencing technology. To develop such methods, new algorithms are required that can quickly extract significantly more structural information from sparse experimental data. This paper presents a new class of signal processing algorithms for nuclear magnetic resonance (NMR) structural biology, based on time-frequency analysis of chemical shift dynamics.
A novel approach to multidimensional NMR analysis is proposed in which the data are interpreted in the time-frequency domain, as opposed to the traditional frequency domain. Time-frequency analysis (TFA) exposes behavior orthogonal to the magnetic coherence transfer pathways, thus affording new avenues of NMR discovery. An implementation yielding new biophysical results is discussed. In particular, we demonstrate the heretofore unknown presence of through-space inter-atomic distance information within 15N-edited heteronuclear single-quantum coherence(15N HSQC) data. A biophysical model explains these results, and is supported by further experiments on simulated spectra.
REFERENCES
Note: OCR errors may be found in this Reference List extracted from the full text article. ACM has opted to expose the complete List rather than only correct and linked references.
 |
1
|
Chris Bailey-Kellogg , Alik Widge , John J. Kelley, III , Marcelo J. Berardi , John H. Bushweller , Bruce Randall Donald, The NOESY jigsaw: automated protein secondary structure and main-chain assignment from sparse, unassigned NMR data, Proceedings of the fourth annual international conference on Computational molecular biology, p.33-44, April 2000, Tokyo, Japan
[doi> 10.1145/332306.332323]
|
| |
2
|
C. Bailey-Kellogg, A. Widge, J. J. Kelley III, M. Berardi, J. Bushweller, B. R. Donald, "The NOESY Jigsaw: Automated Protein Secondary Structure and Main-Chain Assignment from Sparse, Unassigned NMR Data, J. Computational Biology, 7(3-4) (2000) pp. 537-558.
|
| |
3
|
D.E. Zimmerman, C.A. Kulikowski, Y. Huang, W. Feng, M. Tashiro, S. Shimotakahara, C. Chien, R. Powers, and G. Montelione. Automated analysis of protein NMR assignments using methods from artificial intelligence. J. Mol. Bio, 269:592-610, 1997.
|
| |
4
|
C. Bartels, P. Guntert, M. Bileter, and K. Wuthrich. GARANT- a general algorithm for resonance assignment of multidimensional nuclear magnetic resonance spectra. J. Comp. Chem., 18:139-149, 1997
|
| |
5
|
D. Croft, J. Kemmink, K.-P. Neidig, and H. Oschkinat. Tools for the automated assignment of high-resolution three-dimensional protein NMR spectra based on pattern recognition techniques. J. Biomol. NMR, 10:207- 219, 1997
|
| |
6
|
Y. X. Lin and G. Wagner, Efficient side-chain and backbone assignment in large proteins: Application to tGCN5, J. Biomol. NMR, 15 227-239, 1999.
|
| |
7
|
J.A. Cuff, M.E. Clamp, A.S. Siddiqui, M. Finlay, and G.J. Barton. JPRED: A consensus secondary structure prediction server. Bioinformatics, 14:892-893. 1998.
|
| |
8
|
G. Dealeage, B. Tinland, and B. Roux. A computerized version of the Chou and Fasman method for predicting the secondary structure of proteins. Analytical Biochemistry, 163(2):292-297, June 1987
|
| |
9
|
D.S. Wishart, B.D. Sykes, and F.M. Richards. The chemical shift index: a fast and simple method for the assignment of protein secondary structure through NMR spectroscopy. Biochemistry, 31(6):1647-1651, February 1992
|
| |
10
|
K. W~thrich, NMR of Proteins and Nucleic Acids. (John Wiley & Sons, 1986).
|
| |
11
|
J. Cavanagh, W.J. Fairbrother, A.G. Palmer, N.J. Skelton, Protein NMR Spectroscopy: Principles and Practice. 416-418 (Academic Press Inc., 1996).
|
| |
12
|
Sitkoff, D., & Case, D. Density Functional Calculations of Proton Chemical Shifts in Model Peptides. J. Am. Chem Soc. 119, 12262-12273 (1997)
|
| |
13
|
Dejaegere, A. P., Case, D. Density Functional Study of Ribose and Deoxyribose Chemical Shifts, J. Phys. Chem. A 102, 5280-5289 (1998)
|
| |
14
|
Moravetski, V., Hill, J. R., Eichler, U., Sauer, J. 29Si NMR Chemical Shifts of Silicate Species: Ab Initio Study of Environment and Structure Effects, J. Am. Chem. Soc. 118, 13015-13020 (1996)
|
| |
15
|
M. Gerstein and W. Krebs, Nucleic Acids Research 26 (1998).
|
| |
16
|
Serrai, H., L. Senhadji, J. D. de Certaines, and J. L. Coatrieux, Timedomain quantification of amplitude, chemical shift, apparent relaxation time T2, and phase by wavelet-transform analysis. Application to biomedical magnetic resonance spectroscopy J. Magn. Res. 124, 20-34 (1997).
|
| |
17
|
Wagner, G., NMR relaxation and protein mobility, Current Opinion in Struct. Biol., 3, 748-754 (1993)
|
| |
18
|
Palmer, A. G., Williams, J., & McDermott, A. Nuclear Magnetic Resonance Studies of Biopolymer Dynamics, J. Phys. Chem., 100, 13293-13310 (1996)
|
| |
19
|
Lipari, G. & Szabo, A., Model-Free approach to the Interpretation of Nuclear Magnetic Resonance Relaxation in Macromolecules. 1. Theory and Range of Validity, J. Am. Chem. Soc., 104, 4546-4559 (1982)
|
| |
20
|
Palmer, A. G., Dynamic properties of proteins from NMR spectroscopy, Current Opinion in Biotechnology., 4, 385-391 (1993)
|
| |
21
|
Palmer, A. G., Probing molecular motion by NMR, Current Opinion in Struct. Biol., 7, 732-737 (1997)
|
| |
22
|
Lipari, G. & Szabo, A., Model-Free approach to the Interpretation of Nuclear Magnetic Resonance Relaxation in Macromolecules. 2. Analysis of Experimental Results, J. Am. Chem. Soc., 104, 4560-4570 (1982)
|
| |
23
|
Kay, L., Protein Dynamics from NMR, Nature Struct. Biol. NMR Supplement, July (1998)
|
| |
24
|
Palmer, A. G. and Bracken, C. Spin Relaxation Methods for Characterizing Picosecond-nanosecond and microsecond-millisecond motions in Proteins, in NMR in Supramolecular Chemistry, Pons, M. ed. 171-190, (1999 Kluwer Academic Publishers, Netherlands)
|
| |
25
|
|
| |
26
|
Delaglio, F. et al, NMRPipe: a multidimensional spectral processing system based on UNIX Pipes. J. Biomol. NMR. 6 (1995).
|
| |
27
|
Mendel, J. M., Tutorial on Higher-Order Statistics (Spectra) in Signal Processing and System Theory: Theoretical Results and Some Applications, Proc. IEEE, 79 278-305 (1996).
|
| |
28
|
H. Farid, Blind Inverse Gamma Correction, IEEE Trans. on Image Processing
|
| |
29
|
Sun, C., Holmgren, A. & Bushweller, J., Complete 1H, 13C, and 15N NMR resonance assignments and secondary structure of human glutaredoxin in the fully reduced form, Protein Science, 6, 383-390 (1997)
|
| |
30
|
Sun, C., Berardi, M. J., & Bushweller, J., The NMR solution structure of human glutaredoxin in the fully reduced form. J. Mol. Bio 280, p 687 (1998).
|
| |
31
|
Huang, X., Speck, N. A. & Bushweller, J., Complete Resonance Assignments and secondary structure of core binding factor ~, J. Biom. NMR 12, 459-460 (1997).
|
| |
32
|
Huang, X. Peng, J., Speck, N. A. & Bushweller, J., Solution Structure of Core Binding Factor Beta and Map of the CBF-~ Binding Site, Nat Struct Biol. 6 pp. 624 (1999)
|
| |
33
|
Bloch, F., Hansen, W.W. & Packard, M., Nuclear Induction, Phys. Rev. 69,127 (1946).
|
| |
34
|
Wijmenga, S. S., Kruithof, M. & Hilbers, C. W., Analysis of 1H chemical shifts in DNA: Assessment of the reliability of 1H chemical shifts for use in structure refinement. J. Bio NMR 10, 337-350 (1997)
|
| |
35
|
J. Cavanagh, W.J. Fairbrother, A.G. Palmer, N.J. Skelton, Protein NMR Spectroscopy: Principles and Practice. 384-394 (Academic Press Inc., 1996).
|
| |
36
|
Hare B.J., Wyss D.F., Osburne M.S., Kern P.S., Reinherz E.L., Wagner G. Structure, specificity and CDR mobility of a class II restricted singlechain T-cell receptor, Nat Struct Biol 1999 Jun;6(6):574-81
|
| |
37
|
Pearson, J. G., et al Predicting Chemical Shifts in Proteins: Structure Refinement of Valine Residues by Using ab Initio and Empirical Geometry Optimizations, J. Am. Chem. Soc. 119, 11941-11950 (1997)
|
| |
38
|
Osapay, K. & Case, D.A., Peptides, Chemistry, Structure and Biology, R.S. Hodges and J.A. Smith, eds. (Leiden: ESCOM, 1994), pp. 911-913.
|
 |
39
|
Ying Xu , Dong Xu , Oakley H. Crawford , J. Ralph Einstein , Engin Serpersu, Protein structure determination using protein threading and sparse NMR data (extended abstract), Proceedings of the fourth annual international conference on Computational molecular biology, p.299-307, April 2000, Tokyo, Japan
[doi> 10.1145/332306.332568]
|
| |
40
|
Stern, A., and J. C. Hoch, Personal communication (2000).
|
|