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. 2009 Nov 20;192(2):436–445. doi: 10.1128/JB.01040-09

FIG. 2.

FIG. 2.

Mass spectra of farnesylated intermediates. All spectra were obtained using an Applied Biosystems AP 4000 QTrap as specified in Materials and Methods. Intermediates were infused at a concentration of 2 pmol/μl in 80:20 ethanol-hexanes at a flow rate of 20 μl/min. Panel A shows the [RQ3 + H]+ precursor ion (C23H34NO3+; exact mass, 372.2) and the RQ tropylium ion (C9H12NO3+; exact mass, 182.1). Panel B shows the [Q3 + H]+ precursor ion (C24H35O4+; exact mass, 387.2) and the Q tropylium ion (C10H13O4+; exact mass, 197.1). Panel C shows the [DDMQ3 + H]+ precursor ion (C22H31O3+; exact mass, 343.2) and the DDMQ tropylium ion (C8H9O3+; exact mass, 153.1). Panel D shows the [DMQ3 + H]+ precursor ion (C23H33O3+; exact mass, 357.2) and the DMQ tropylium ion (C9H11O3+; exact mass, 167.2). Panel E shows the [DMeQ3 + H]+ precursor ion (C23H33O4+; exact mass, 373.2) and the DMeQ tropylium ion (C9H11O4+; exact mass, 183.1; the base peak for this compound is highly collision energy dependent).