TY - JOUR
T1 - Using single lectins to enrich glycoproteins in conditioned media
AU - Sethi, Manveen K.
AU - Fanayan, Susan
PY - 2015
Y1 - 2015
N2 - Lectins are sugar-binding proteins that can recognize and bind to carbohydrates conjugated to proteins and lipids. Coupled with mass spectrometry technologies, lectin affinity chromatography is becoming a popular approach for identification and quantification of glycoproteins in complex samples such as blood, tumor tissues, and cell lines. Given the commercial availability of a large number of lectins that recognize diverse sugar structures, it is now possible to isolate and study glycoproteins for biological and medical research. This unit provides a general guide to single-lectin-based enrichment of glycoproteins from serum-free conditioned media. Due to the unique carbohydrate specificity of most lectins and the complexity of the samples, optimization steps may be required to evaluate different elution buffers and methods as well as binding conditions, for each lectin, for optimal recovery of bound glycoproteins.
AB - Lectins are sugar-binding proteins that can recognize and bind to carbohydrates conjugated to proteins and lipids. Coupled with mass spectrometry technologies, lectin affinity chromatography is becoming a popular approach for identification and quantification of glycoproteins in complex samples such as blood, tumor tissues, and cell lines. Given the commercial availability of a large number of lectins that recognize diverse sugar structures, it is now possible to isolate and study glycoproteins for biological and medical research. This unit provides a general guide to single-lectin-based enrichment of glycoproteins from serum-free conditioned media. Due to the unique carbohydrate specificity of most lectins and the complexity of the samples, optimization steps may be required to evaluate different elution buffers and methods as well as binding conditions, for each lectin, for optimal recovery of bound glycoproteins.
UR - http://www.scopus.com/inward/record.url?scp=84949189855&partnerID=8YFLogxK
U2 - 10.1002/0471140864.ps2406s81
DO - 10.1002/0471140864.ps2406s81
M3 - Article
C2 - 26237673
AN - SCOPUS:84949189855
VL - 2015
SP - 24.6.1-24.6.10
JO - Current Protocols in Protein Science
JF - Current Protocols in Protein Science
SN - 1934-3655
ER -