Vestal Marvin L, Campbell Jennifer M
Applied Biosystems, Framingham, Massachusetts, USA.
Methods Enzymol. 2005;402:79-108. doi: 10.1016/S0076-6879(05)02003-3.
A new tandem time-of-flight (TOF-TOF) instrument has been developed by modifying a standard matrix-assisted laser desorption ionization (MALDI)-TOF instrument to make high-performance, high-energy collision-induced dissociation (CID) MALDI tandem mass spectrometry (MS) a practical reality. To optimize fragment spectra quality, the selected precursor ion is decelerated before entering a floating collision cell and the potential difference between the source and the collision cell defines the collision energy of the ions. Standard operating conditions for tandem MS use a 1-kV collision energy with single-collision conditions and increased laser power for ion formation. Hence, both high- and low-energy fragments are observed in MALDI TOF-TOF spectra. On standard peptides, sensitivities down to 1 fmol are demonstrated. On a mixture of two solution tryptic digests at the 25-fmol level, 23 spectra were sufficient to result in proper database identification.
通过对标准基质辅助激光解吸电离(MALDI)-飞行时间(TOF)仪器进行改进,开发出了一种新型串联飞行时间(TOF-TOF)仪器,从而使高性能、高能碰撞诱导解离(CID)MALDI串联质谱(MS)成为现实。为了优化碎片谱质量,选定的前体离子在进入浮动碰撞池之前会减速,源与碰撞池之间的电位差决定了离子的碰撞能量。串联质谱的标准操作条件是在单碰撞条件下使用1 kV的碰撞能量,并增加用于离子形成的激光功率。因此,在MALDI TOF-TOF谱中可以观察到高能和低能碎片。对于标准肽,灵敏度可低至1 fmol。在25 fmol水平的两种溶液胰蛋白酶消化物的混合物上,23个谱就足以实现正确的数据库鉴定。