Basi N S, Rebois R V
Membrane Biochemistry Section, NINDS, NIH, Bethesda, Maryland 20892, USA.
Anal Biochem. 1997 Aug 15;251(1):103-9. doi: 10.1006/abio.1997.2255.
Rate zonal sedimentation gives information about the shape and size of proteins, and is useful for investigating protein-protein interactions. However, rate zonal sedimentation experiments typically last approximately 1 day. In contrast, this report describes a rate zonal sedimentation method requiring 1 h or less. This was accomplished by centrifuging small density gradients (200 microliters) prepared with sucrose or OptiPrep in a fixed-angle rotor at high relative centrifugal force. By using small gradient volumes, the sample dilution that occurs with larger gradients and with many chromatographic techniques was also avoided. For a variety of proteins, plots of S20,w versus distance sedimented during centrifugation in a TLA 120.2 rotor were linear. As a practical application, sedimentation of the heterotrimeric stimulatory G protein and its dissociated alpha-subunit were determined. The results were similar to those obtained with 17- to 22-h centrifugations in an SW 50.1 rotor and agreed with previously published values. Long periods of centrifugation might preclude the study of some unstable proteins or the investigation of protein-protein interactions whose affinities are to low to survive the lengthy centrifugations required to carry out traditional rate zonal sedimentation experiments. A rate zonal sedimentation technique that rivals many chromatographic methods in celerity will help to circumvent these problems.
速率区带沉降法可提供有关蛋白质形状和大小的信息,有助于研究蛋白质 - 蛋白质相互作用。然而,速率区带沉降实验通常持续约1天。相比之下,本报告描述了一种耗时1小时或更短时间的速率区带沉降方法。这是通过在固定角度转头中以高相对离心力离心用蔗糖或OptiPrep制备的小密度梯度(200微升)来实现的。通过使用小梯度体积,还避免了较大梯度以及许多色谱技术中出现的样品稀释。对于多种蛋白质,在TLA 120.2转头中离心时,S20,w与沉降距离的关系图呈线性。作为实际应用,测定了异源三聚体刺激性G蛋白及其解离的α亚基的沉降情况。结果与在SW 50.1转头中进行17至22小时离心所获得的结果相似,并且与先前发表的值一致。长时间离心可能会妨碍对某些不稳定蛋白质的研究,或妨碍对亲和力过低而无法在传统速率区带沉降实验所需的长时间离心过程中存活的蛋白质 - 蛋白质相互作用的研究。一种在速度上可与许多色谱方法相媲美的速率区带沉降技术将有助于解决这些问题。