Mallis Christopher S, Zheng Xueyun, Qiu Xi, McCabe Jacob W, Shirzadeh Mehdi, Lyu Jixing, Laganowsky Arthur, Russell David H
Department of Chemistry, Texas A&M University, College Station, TX 77843.
Agilent Technologies, Inc., Wilmington, DE 19808.
Int J Mass Spectrom. 2020 Dec;458. doi: 10.1016/j.ijms.2020.116451. Epub 2020 Oct 9.
Native mass spectrometry (nMS) is increasingly used for studies of large biomolecules (>100 kDa), especially proteins and protein complexes. The growth in this area can be attributed to advances in native electrospray ionization as well as instrumentation that is capable of accessing high mass-to-charge () regimes without significant losses in sensitivity and resolution. Here, we describe modifications to the ESI source of an Agilent 6545XT Q-TOF MS that is tailored for analysis of large biomolecules. The modified ESI source was evaluated using both soluble and membrane protein complexes ranging from ~127 to ~232 kDa and the ~801 kDa protein chaperone GroEL. The increased mass resolution of the instrument affords the ability to resolve small molecule adducts and analyze collision-induced dissociation products of the native complexes.
原生质谱(nMS)越来越多地用于研究大分子(>100 kDa),尤其是蛋白质和蛋白质复合物。该领域的发展得益于原生电喷雾电离技术的进步以及能够在不显著损失灵敏度和分辨率的情况下进入高质量电荷比(m/z)范围的仪器设备。在此,我们描述了对安捷伦6545XT Q-TOF质谱仪的电喷雾电离(ESI)源进行的改进,该改进是为分析大分子量身定制的。使用分子量范围约为127至232 kDa的可溶性和膜蛋白复合物以及约801 kDa的蛋白质伴侣GroEL对改进后的ESI源进行了评估。仪器提高的质量分辨率使其能够分辨小分子加合物并分析原生复合物的碰撞诱导解离产物。