North C L, Franklin J C, Bryant R G, Cafiso D S
Department of Chemistry, University of Virginia, Charlottesville 22901.
Biophys J. 1994 Nov;67(5):1861-6. doi: 10.1016/S0006-3495(94)80667-8.
A nitroxide spin label attached to the C-terminus of the channel forming peptide alamethicin produces an enhancement of the nuclear spin-lattice relaxation rates of peptide protons as a result of both intermolecular and intramolecular magnetic dipole-dipole interactions. The intermolecular contribution provides evidence that alamethicin monomers collide preferentially in a C-terminal-to-N-terminal configuration in methanol. From the intramolecular paramagnetic enhancement of nuclear spin-lattice relaxation times, effective distances between the unpaired electron on the nitroxide at the C-terminus of alamethicin and protons along the peptide backbone were calculated. These distances are much shorter than distances based on the reported crystal structure of alamethicin, and cannot be accounted for by motion in the bonds that attach the nitroxide to the peptide. In addition, the differences between distances deduced from the nuclear spin relaxation and the distances seen in the crystal structure increase toward the N-terminal end of the peptide. The simplest explanation for these data is that the alamethicin backbone suffers large structural fluctuations that yield shorter effective distances between the C-terminus and positions along the backbone. This finding can be interpreted in terms of a molecular mechanism for the voltage-gating of the alamethicin channel. When the distances between a paramagnetic center and a nucleus fluctuate, paramagnetic enhancements are expected to yield distances that are weighted by r-6, and distances calculated using the Solomon-Bloembergen equations may more nearly represent a distance of closest approach than a time average distance. Therefore, the use of paramagnetic centers such as spin labels or metal ions with long electron T1 values provides a distance measurement that reflects a dynamically averaged structure where the averaging process heavily weights short distances. The results of such measurements, when combined with other structural information, may provide particularly clear evidence for the magnitude of structural fluctuations involving distances greater than 10 A.
附着于通道形成肽短杆菌肽C末端的氮氧化物自旋标记,由于分子间和分子内磁偶极-偶极相互作用,导致肽质子的核自旋-晶格弛豫速率增强。分子间的贡献提供了证据,表明短杆菌肽单体在甲醇中优先以C末端到N末端的构型碰撞。根据核自旋-晶格弛豫时间的分子内顺磁增强,计算了短杆菌肽C末端氮氧化物上未配对电子与沿肽主链质子之间的有效距离。这些距离比基于报道的短杆菌肽晶体结构的距离短得多,并且不能用将氮氧化物连接到肽的键中的运动来解释。此外,从核自旋弛豫推导出的距离与晶体结构中观察到的距离之间的差异朝着肽的N末端增加。对这些数据最简单的解释是,短杆菌肽主链存在较大的结构波动,导致C末端与沿主链位置之间的有效距离更短。这一发现可以用短杆菌肽通道电压门控的分子机制来解释。当顺磁中心与原子核之间的距离发生波动时,顺磁增强预计会产生按r-6加权的距离,并且使用所罗门-布洛姆伯根方程计算的距离可能更接近表示最接近的距离而不是时间平均距离。因此,使用具有长电子T1值的顺磁中心,如自旋标记或金属离子,提供了一种距离测量方法,该方法反映了一种动态平均结构,其中平均过程对短距离有很大的权重。当与其他结构信息结合时,这种测量结果可能为涉及大于10 Å距离的结构波动幅度提供特别清晰的证据。