3D NMR Experiments for Measuring15N Relaxation Data of Large Proteins: Application to the 44 kDa Ectodomain of SIV gp41
✍ Scribed by Michael Caffrey; Joshua Kaufman; Stephen J. Stahl; Paul T. Wingfield; Angela M. Gronenborn; G.Marius Clore
- Publisher
- Elsevier Science
- Year
- 1998
- Tongue
- English
- Weight
- 134 KB
- Volume
- 135
- Category
- Article
- ISSN
- 1090-7807
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✦ Synopsis
A suite of 3D NMR experiments for measuring 15N-¿1H¿ NOE, 15N T1, and 15N T1rho values in large proteins, uniformly labeled with 15N and 13C, is presented. These experiments are designed for proteins that exhibit extensive spectral overlap in the 2D 1H-15N HSQC spectrum. The pulse sequences are readily applicable to perdeuterated samples, which increases the spectral resolution and signal-to-noise ratio, thereby permitting the characterization of protein dynamics to be extended to larger protein systems. Application of the pulse sequences is demonstrated on a perdeuterated 13C/15N-labeled sample of the 44 kDa ectodomain of SIV gp41.