SialEXO™ – Hydrolysis of Sialic Acids

The SialEXO products are sialidases for the removal and analysis of sialic acids. The enzymes are active on both N- and O-linked glycans present on native glycoproteins or released glycan structures.

SmartEnzymes™

SialEXO is used to pretreat O-glycosylated proteins prior to digestion with OpeRATOR or OglyZOR. Other applications include reduction of sample complexity, charge variant analyses and exoglycosidase arrays.

Why SialEXO™?

  • Efficient desialylation of N-linked, O-linked and released glycans
  • Fast removal of sialic acids for enhanced analysis of protein charge variants
  • Available immobilized in ready-to-use spin columns
  • Target

    Sialic acids on N- and O-linked glycans

  • Time

    30 min - 2 h reaction

  • Box

    No need for co-factors

  • Digestion Site

    α2-3, α2-6 and α2-8-linked sialic acids

Product Formats

About SialEXO™

The SialEXO products are sialidases for efficient desialylation of N- and O-glycosylated proteins.

SialEXO Lyophilized consists of two sialidases, each having unique activities and they work simultaneously. One enzyme has a broad activity for α2-3, α2-6 and α2-8-linked sialic acids, and the other one (SialEXO 2-3) quickly hydrolyzes sialic acids with α2-3-linkage. SialEXO Lyophilized removes all sialic acids on native proteins within 2 h.

SialEXO hydrolyzes glycoproteins under native conditions and displays activity in pH ranging from 6.5 to 9.

The enzymes are derived from Akkermansia muciniphila and expressed in E. coli. Both enzymes contain a His-tag and the molecular weights of the enzymes are 43 kDa and 66 kDa.

Applications

Performance Activity

Resources

FAQ and Support

Yes, SialEXO can be incubated together with OpeRATOR and/or OglyZOR in 20 mM Tris pH 6.8.

Yes, SialEXO displays activity on sialic acids with α2-3, α2-6 and α2-8 linked bonds of both N- and O-glycans.

Yes, SialEXO contains a 6x His-tag.

Yes, both enzymes are active under native conditions, preferably use 20 mM Tris pH 7. If denaturing reaction conditions are required for PNGaseF, the reaction with SialEXO needs to be performed first under native conditions, then add PNGaseF and the required buffer.

No, SialEXO works both on glycoproteins in native conditions but can also be used on denatured proteins after buffer exchange.