Peterson J, Day E P, Pearce L L, Wilson M T
Department of Chemistry, University of Alabama, Tuscaloosa 35487-0336.
Biochem J. 1995 Feb 1;305 ( Pt 3)(Pt 3):871-8. doi: 10.1042/bj3050871.
A protocol for obtaining high-quality saturation-magnetization data from metalloprotein samples, employing a superconducting quantum interference device (SQUID) magnetometer, has previously been reported [E. P. Day, T. A. Kent, P. A. Lindahl, E. Münck, W. H. Orme-Johnson, H. Roder and A. Roy (1987) Biophys. J. 52, 837-853 and E. P. Day (1993) Methods Enzymol. 227, 437-463]. Following studies of several dozen different metalloprotein derivatives, the methodology has been further refined, particularly in the area of sample preparation. The details of the sample-handling procedures now in use are described, and moreover, the critical issue of verifying that contamination by paramagnetic impurities remains insignificant is considered. Importantly, it is shown that an independent determination of the quantity of paramagnetic sample present in the magnetometer is undesirable. Much more reliable parameters concerning the ground-state magnetic properties of the system under study are obtained if enough saturation-magnetization data are collected to enable the spin concentration to be determined during the subsequent fitting procedure. As proof of the validity of this method, the results of magnetization studies on ferricytochrome c, ferrocytochrome c and the benzohydroxamic acid adduct of horseradish peroxidase are presented. The ability of saturation-magnetization measurements to routinely determine spin concentration to within +/- 4% of accepted values is firmly established. In addition, a saturation-magnetization study has been performed on resting and fully reduced derivatives of cytochrome c oxidase. These results provide an illustration of the usefulness of the technique in probing some systems which have proved difficult to study by other methods. The increased difficulties inherent in obtaining meaningful data from these cytochrome c oxidase and other integer spin systems are delineated.
此前已有报道一种利用超导量子干涉器件(SQUID)磁力计从金属蛋白样品中获取高质量饱和磁化数据的方案[E.P.戴伊、T.A.肯特、P.A.林达尔、E.明克、W.H.奥姆-约翰逊、H.罗德和A.罗伊(1987年)《生物物理杂志》52卷,837 - 853页;E.P.戴伊(1993年)《酶学方法》227卷,437 - 463页]。在对几十种不同的金属蛋白衍生物进行研究之后,该方法得到了进一步完善,尤其是在样品制备方面。本文描述了目前所使用的样品处理程序的细节,此外,还考虑了验证顺磁性杂质污染仍可忽略不计这一关键问题。重要的是,研究表明,对磁力计中存在的顺磁性样品的量进行独立测定是不可取的。如果收集到足够的饱和磁化数据,以便在后续拟合过程中确定自旋浓度,就可以获得关于所研究系统基态磁性的更可靠参数。作为该方法有效性的证明,本文给出了对铁细胞色素c、亚铁细胞色素c以及辣根过氧化物酶的苯并异羟肟酸加合物的磁化研究结果。饱和磁化测量能够常规地将自旋浓度确定在公认值的±4%以内,这一点得到了有力证实。此外,还对细胞色素c氧化酶的静止态和完全还原态衍生物进行了饱和磁化研究。这些结果说明了该技术在探测一些用其他方法难以研究的系统方面的有用性。文中阐述了从这些细胞色素c氧化酶和其他整数自旋系统中获取有意义数据所固有的增加的困难。