Glyko® 2-AB-α(2-6) Sialylated Triantennary Library [GKSB-263]

Price:
$ 400.00

Description


The Glyko® 2-AB-α(2-6) Sialylated Triantennary Library consists of triantennary oligosaccharides containing α(2-6) linked sialic acid.  The reducing termini are derivatized with the fluorescent dye, 2-aminobenzamide (2-AB).

Please contact us for a representative Certificate of Analysis.

The α(2-6) sialic acid linkage is the predominant linkage type on human intravenous immunoglobulin (IVIG) IgG Fc N-glycans [1].  This differs from glycoproteins produced in Chinese hamster ovary (CHO) cells, where N-glycans are α(2-3)-sialylated [2].  Depending on the separation method, it may be possible to resolve α(2-3) and α(2-6) sialic acid linkage isomers.  For example, α(2-3)-sialylated N-glycans are known to have a shorter HILIC retention time than isomeric N-glycans with α(2-6) sialic acid linkages [3,4].  Sialic acid linkage position may also be determined by exoglycosidase digests with Sialidase S (GK80021), which releases non-reducing terminal α(2-3)-linked sialic acid, and sialidase A (GK80040) which releases α(2-3,6,8,9)-linked sialic acid.

Size: 200 pmol

Product Code: GKSB-263

References:

  1. Anthony RM, Nimmerjahn F, Ashline DJ, Reinhold VN, Paulson JC, Ravetch JV. Recapitulation of IVIG anti-inflammatory activity with a recombinant IgG Fc.  2008 Apr 18;320(5874):373-6. 
  2. Lee EU, Roth J, Paulson JC. Alteration of terminal glycosylation sequences on N-linked oligosaccharides of Chinese hamster ovary cells by expression of beta-galactoside alpha 2,6-sialyltransferase.  1989 Aug 15;264(23):13848-55.
  3. Raymond C, Robotham A, Spearman M, Butler M, Kelly J, Durocher Y. Production of α2,6-sialylated IgG1 in CHO cells.  2015;7(3):571-83. 
  4. GlycoBase 3.2.4. [Internet]. Blackrock, Ireland: National Institute for Bioprocessing Research and Training (NIBRT); c2012. All Collections including digests (93); [cited 2016 Apr 12]. Available from: https://glycobase.nibrt.ie/glycobase/browse_glycans.action
Structures

The table below indicates the N-glycans typically contained in this library in order of HILIC retention time (shortest to longest) using QC HILIC methods. Due to variability in starting material, actual glycans identified in each lot may be subject to change. If you would like more information about our current lot(s), please contact us.

N-Glycans of 2-AB-α(2-6) Sialylated Triantennary Library:

Glycan Identification ProZyme Oxford (New) [1] Structure [2]
Asialo, galactosylated triantennary NA3 A3G(4)3
Mono-α(2-6)-sialylated, galactosylated triantennary NA3S1 A3G(4)3S(3)1
Di-α(2-6)-sialylated, galactosylated triantennary NA3S2 A3G(4)3S(3)2
Tri-α(2-6)-sialylated, galactosylated triantennary A3 A3G(4)3S(3)3

Structure Key [2]:

Structures drawn using GlycoWorkbench[3]. 

References:

  1. GlycoBase 3.2.4. [Internet]. Blackrock, Ireland: National Institute for Bioprocessing Research and Training (NIBRT); c2012. Guide to the abbreviations used to identify 2AB labelled N-glycans; [cited 2016 Apr 19].  Available from: www.glycobase.nibrt.ie/glycobase/documents/abbreviations.pdf
  2. Harvey DJ, Merry AH, Royle L, Campbell MP, Dwek RA, Rudd PM. Proposal for a standard system for drawing structural diagrams of N- and O-linked carbohydrates and related compounds.  2009 Aug;9(15):3796-801
  3. Ceroni A, Maass K, Geyer H, Geyer R, Dell A, Haslam SM. GlycoWorkbench: a tool for the computer-assisted annotation of mass spectra of glycans.  2008 Apr;7(4):1650-9.
Safety

Product Safety Documentation for GKSB-263:

Product/Part No. Description
GKSB-263 Glyko® 2-AB-α(2-6) Sialylated Triantennary Library 

 


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