TY - JOUR
T1 - Gel-forming and cell-associated mucins: Preparation for structural and functional studies
AU - Davies, Julia R.
AU - Wickström, Claes
AU - Thornton, David J.
N1 - , Biotechnology and Biological Sciences Research Council, United Kingdom, Medical Research Council, United Kingdom, Wellcome Trust, United Kingdom
PY - 2012
Y1 - 2012
N2 - Secreted and transmembrane mucins are important components of innate defence at the body's mucosal surfaces. The secreted mucins are large, polymeric glycoproteins, which are largely responsible for the gel-like properties of mucus secretions. The cell-tethered mucins, however, are monomeric but are typically composed of two subunits, a larger extracellular subunit which is heavily glycosylated while the smaller more sparsely glycosylated subunit has a short extracellular region, a single-pass transmembrane domain, and a cytoplasmic tail. These two families of mucins represent high-molecular-weight glycoproteins containing serine and threonine-rich domains that are the attachment sites for large numbers of O-glycans. The high-M r and high sugar content have been exploited for the separation of mucins from the majority of components in mucus secretions. In this chapter, we describe current and well-established methods (caesium chloride density-gradient centrifugation, gel-filtration and anion-exchange chromatography, and agarose gel electrophoresis) for the extraction and purification of gel-forming and cell-surface mucins which can subsequently be used for a variety of structural and functional studies. © 2012 Springer Science+Business Media, LLC.
AB - Secreted and transmembrane mucins are important components of innate defence at the body's mucosal surfaces. The secreted mucins are large, polymeric glycoproteins, which are largely responsible for the gel-like properties of mucus secretions. The cell-tethered mucins, however, are monomeric but are typically composed of two subunits, a larger extracellular subunit which is heavily glycosylated while the smaller more sparsely glycosylated subunit has a short extracellular region, a single-pass transmembrane domain, and a cytoplasmic tail. These two families of mucins represent high-molecular-weight glycoproteins containing serine and threonine-rich domains that are the attachment sites for large numbers of O-glycans. The high-M r and high sugar content have been exploited for the separation of mucins from the majority of components in mucus secretions. In this chapter, we describe current and well-established methods (caesium chloride density-gradient centrifugation, gel-filtration and anion-exchange chromatography, and agarose gel electrophoresis) for the extraction and purification of gel-forming and cell-surface mucins which can subsequently be used for a variety of structural and functional studies. © 2012 Springer Science+Business Media, LLC.
KW - Agarose gel electrophoresis
KW - Anion-exchange chromatography
KW - Density-gradient centrifugation
KW - Gel-filtration chromatography
KW - Guanidinium chloride
KW - Mucin
KW - Mucin extraction
KW - Mucin purification
U2 - 10.1007/978-1-61779-513-8_2
DO - 10.1007/978-1-61779-513-8_2
M3 - Article
C2 - 22259128
SN - 1064-3745
VL - 842
SP - 27
EP - 47
JO - Methods in Molecular Biology
JF - Methods in Molecular Biology
ER -