4.7 Article

Combined Molecular and Elemental Mass Spectrometry Approaches for Absolute Quantification of Proteomes: Application to the Venomics Characterization of the Two Species of Desert Black Cobras, Walterinnesia aegyptia and Walterinnesia morgani

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 20, Issue 11, Pages 5064-5078

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jproteome.1c00608

Keywords

snake venomics; combined top-down and bottom-up venomics; hybrid elemental and molecular mass spectrometry; absolute quantification of venom proteome; desert black cobra; Walterinnesia aegyptia; Walterinnesia morgani

Funding

  1. (MCIU/AEI/FEDER, UE), Madrid, Spain [PGC2018-098290-B-I00]
  2. Ministerio de Ciencia e Innovacion, Madrid, Spain [BFU201789103-P, PID2019-109698GB-I00]
  3. Technische Universitat Berlin by the Department of International Scientific Cooperation
  4. Agilent Technologies

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This study presents a novel hybrid, molecular and elemental mass spectrometry setup for the absolute quantification of snake venom proteomes, providing accurate information on two species within the genus Walterinnesia, Walterinnesia aegyptia and Walterinnesia morgani. Through an experimental design that includes decomplexation of venom samples and protein identification and elemental mass spectrometry, the study offers quantitative and specific insights into the venom proteomes. The results also validate the units of measure for relative quantification of snake venom proteomes and suggest broader applications of hybrid elemental/molecular MS setups in proteomics.
We report a novel hybrid, molecular and elemental mass spectrometry (MS) setup for the absolute quantification of snake venom proteomes shown here for two desert black cobra species within the genus Walterinnesia, Walterinnesia aegyptia and Walterinnesia morgani. The experimental design includes the decomplexation of the venom samples by reverse-phase chromatography independently coupled to four mass spectrometry systems: the combined bottom-up and top-down molecular MS for protein identification and a parallel reverse-phase microbore high-performance liquid chromatograph (RP-mu HPLC) on-line to inductively coupled plasma (ICP-MS/MS) elemental mass spectrometry and electrospray ionization quadrupole time-of-flight mass spectrometry (ESI-QToF MS). This allows to continuously record the absolute sulfur concentration throughout the chromatogram and assign it to the parent venom proteins separated in the RP-mu HPLC-ESI-QToF parallel run via mass profiling. The results provide a locus-resolved and quantitative insight into the three desert black cobra venom proteome samples. They also validate the units of measure of our snake venomics strategy for the relative quantification of snake venom proteomes as % of total venom peptide bonds as a proxy for the % by weight of the venom toxins/toxin families. In a more general context, our work may pave the way for broader applications of hybrid elemental/molecular MS setups in diverse areas of proteomics.

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