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Studies of Malaria by Mass Spectrometry

Applied Physics Laboratory, Johns Hopkins University, Laurel, MD 20723 [Pg.161]

Identification of Microorganisms by Mass Spectrometry, Edited by Charles L. Wilkins and Jackson O. Lay, Jr. [Pg.161]

Detection by LDMS and structural elucidation of other secondary metabolite products, generated in the host during the onset of the parasite disease, is discussed. These molecules may serve as additional biomarkers for rapid malaria diagnosis by LDMS. For instance, choline phosphate (CP) is identified as the source of several low-mass ions observed in parasite-infected blood samples in addition to heme biomarker ions. The CP levels track the sample parasitemia levels. This biomarker can provide additional specificity and sensitivity when compared to malaria detection based on heme ion signals alone. Furthermore the observed elevated CP levels are discussed in the context of Plasmodium metabolism during its intra-erythrocytic life cycle. These data can [Pg.162]


See other pages where Studies of Malaria by Mass Spectrometry is mentioned: [Pg.161]    [Pg.162]    [Pg.164]    [Pg.166]    [Pg.168]    [Pg.170]    [Pg.172]    [Pg.174]    [Pg.176]    [Pg.178]    [Pg.180]    [Pg.308]    [Pg.161]    [Pg.162]    [Pg.164]    [Pg.166]    [Pg.168]    [Pg.170]    [Pg.172]    [Pg.174]    [Pg.176]    [Pg.178]    [Pg.180]    [Pg.308]    [Pg.162]    [Pg.380]    [Pg.1351]   


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