Journal of Biomolecular NMR

, Volume 62, Issue 3, pp 387–401 | Cite as

Accessible surface area from NMR chemical shifts

Article

Abstract

Accessible surface area (ASA) is the surface area of an atom, amino acid or biomolecule that is exposed to solvent. The calculation of a molecule’s ASA requires three-dimensional coordinate data and the use of a “rolling ball” algorithm to both define and calculate the ASA. For polymers such as proteins, the ASA for individual amino acids is closely related to the hydrophobicity of the amino acid as well as its local secondary and tertiary structure. For proteins, ASA is a structural descriptor that can often be as informative as secondary structure. Consequently there has been considerable effort over the past two decades to try to predict ASA from protein sequence data and to use ASA information (derived from chemical modification studies) as a structure constraint. Recently it has become evident that protein chemical shifts are also sensitive to ASA. Given the potential utility of ASA estimates as structural constraints for NMR we decided to explore this relationship further. Using machine learning techniques (specifically a boosted tree regression model) we developed an algorithm called “ShiftASA” that combines chemical-shift and sequence derived features to accurately estimate per-residue fractional ASA values of water-soluble proteins. This method showed a correlation coefficient between predicted and experimental values of 0.79 when evaluated on a set of 65 independent test proteins, which was an 8.2 % improvement over the next best performing (sequence-only) method. On a separate test set of 92 proteins, ShiftASA reported a mean correlation coefficient of 0.82, which was 12.3 % better than the next best performing method. ShiftASA is available as a web server (http://shiftasa.wishartlab.com) for submitting input queries for fractional ASA calculation.

Keywords

Nuclear magnetic resonance Chemical-shifts Machine learning Accessible surface area Protein 

Supplementary material

10858_2015_9957_MOESM1_ESM.pdf (2 mb)
Supplementary material 1 (PDF 2064 kb)

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Copyright information

© Springer Science+Business Media Dordrecht 2015

Authors and Affiliations

  • Noor E. Hafsa
    • 1
  • David Arndt
    • 1
  • David S. Wishart
    • 1
    • 2
  1. 1.Department of Computing ScienceUniversity of AlbertaEdmontonCanada
  2. 2.Department of Biological SciencesUniversity of AlbertaEdmontonCanada

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