Nonionic, redox-cleavable surfactant for mass spectrometry-based proteomics and structural biological applications
OwnerKyle BROWN, Song JIN +2inventors
InventorsKyle BROWN, Song JIN, Ying GE, Morgan GUGGER
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OwnerKyle BROWN, Song JIN +2inventors
InventorsKyle BROWN, Song JIN, Ying GE, Morgan GUGGER
Estimating the term…
The present invention provides nonionic cleavable surfactants (NCS), specifically n-Decyl-disulfide-β-D-maltoside (DSSM), suitable for MS-based proteomics and analysis. These surfactants are designed to mimic the properties of a commonly used surfactant in structural biology, n-dodecyl-β-d-maltoside (DDM), but contain a disulfide bond that allows for facile cleavage and surfactant removal before analysis. DSSM and other NCS are compatible with native mass spectrometry, top-down and bottom-up proteomics, ESI-MS and other analytical techniques, and reduce signal suppression typically observed with other surfactants. DSSM and other NCS provide versatile surfactants that can facilitate protein sample preparation under non-denaturing conditions for a myriad of proteomic and structural biology applications and act as a general replacement for DDM.
A chemically-cleavable surfactant comprising:
A method of solubilizing a compound comprising the steps of:
A method for analyzing a compound comprising the steps of:
Dependencies are inferred from the claim text.