Van Dorsselaer A, Bitsch F, Green B, Jarvis S, Lepage P, Bischoff R, Kolbe V J, Roitsch C
Laboratoire de Chimie Organique des Substances Naturelles, URA31 CNRS, 67084 Strasbourg, France.
Biomed Environ Mass Spectrom. 1990 Nov;19(11):692-704. doi: 10.1002/bms.1200191108.
Mass measurement by electrospray mass spectrometry (ESMS) is used as a rapid preliminary verification of the identity of various recombinant proteins ranging from 7 to 44 kDa with an accuracy of 0.01-0.03%. ESMS not only improves the speed but also the reliability of the protein structure determination when used in conjunction with other methods of protein analysis. Modifications of these large molecules, for example the loss of C-terminal amino acids, N-terminal acetylation, 2-mercaptoethanol addition to a cysteine, and trace formation of a covalent dimer (3%), are easily detected individually or in mixtures by mass measurement using ESMS; feats which would be very difficult to achieve using classical biochemical methods. As little as 1% of several structurally related protein contaminants have been identified in a 15 kDa recombinant protein preparation.
通过电喷雾质谱法(ESMS)进行质量测量,可用于快速初步验证各种分子量在7至44 kDa之间的重组蛋白的身份,其准确度为0.01 - 0.03%。当与其他蛋白质分析方法结合使用时,ESMS不仅提高了速度,还提高了蛋白质结构测定的可靠性。这些大分子的修饰,例如C端氨基酸的缺失、N端乙酰化、向半胱氨酸添加2-巯基乙醇以及共价二聚体的微量形成(3%),通过使用ESMS进行质量测量,能够轻松地单独或混合检测出来;而这些是使用经典生化方法很难实现的。在一种15 kDa的重组蛋白制剂中,已鉴定出低至1%的几种结构相关的蛋白质污染物。