Explicit treatment of spin labels in modeling of distance constraints from dipolar EPR and DEER

J Am Chem Soc. 2005 Jul 6;127(26):9334-5. doi: 10.1021/ja051652w.

Abstract

Current SDSL-EPR methods allow measurement of dipolar distances in the 8-70 A range; however, the use of extrinsic probes complicates the interpretation of these distances in modeling macromolecular structure and conformational changes. The data presented here show that interprobe distances correlate only weakly with Cbeta-Cbeta distances, especially for distances that are on the order of the spin label tether lengths. Explicitly incorporating the spin label into the modeling process increases the experiment/model correlation 4-fold and reduces the distance error from 6 A to 3 A.

Publication types

  • Comparative Study

MeSH terms

  • Carbon / chemistry
  • Crystallography, X-Ray
  • Electron Spin Resonance Spectroscopy / methods*
  • Monte Carlo Method
  • Protein Conformation
  • Proteins / chemistry*
  • Spin Labels*

Substances

  • Proteins
  • Spin Labels
  • Carbon