Short-range ENDOR distance measurements between Gd(III) and trifluoromethyl labels in proteins.

The measurement of distances in proteins can be challenging in the 5-20 Å range, which is outside those accessible through conventional NMR and EPR methods. Recently it was demonstrated that distances in this range could be measured between a nitroxide as a paramagnetic spin label and a nearby fluorine atom ( 19 F) as a nuclear spin label using high-field (W-band/3.4 T) ENDOR spectroscopy. Here we show that such measurements can also be performed using a gadolinium ion (Gd 3+ ) as the paramagnetic tag. Gd 3+ has two advantages. (i) A greater electronic spin ( S = 7/2) and fast electronic spin-lattice ( T 1 ) relaxation, improving sensitivity by allowing data to be collected at lower temperatures. (ii) A narrow EPR signal for the -½ ↔ ½ transition, and therefore no orientation selection artefacts. Signal intensities can be further enhanced by using a trifluoromethyl (C 19 F 3 ) group instead of a single 19 F atom. Using the protein calbindin D 9k with a Ca 2+ ion replaced by a Gd 3+ ion and a trifluoromethylphenylalanine in position 50, we show that distances up to about 10 Å can be readily measured. Longer distances proved more difficult to measure due to variable electronic T M relaxation rates, which lead to broader Lorentzian ENDOR lineshapes. Gd 3+ complexes (Gd 3+ tags), which reliably display longer T M times, allow longer distances to be measured (8-16 Å). We also provide preliminary evidence that the intensity of ENDOR signals follows the predicted 1/ r 6 dependence, indicating that distances r > 20 Å can be measured by this method.