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Keratan sulfate

About: Keratan sulfate is a research topic. Over the lifetime, 1253 publications have been published within this topic receiving 57984 citations. The topic is also known as: keratan sulfate & KS.


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Journal ArticleDOI
25 Mar 2022-Biology
TL;DR: This work presents an optimized strategy to analyze on-target derivatized CS/DS disaccharides via MALDI-TOF-MS using a fast workflow that does not require any purification after enzymatic cleavage, and shows for the first time that MAL DI-TOf/TOF experiments allow for discrimination between monosulfated CS disac charides via specific fragments corresponding to glycosidic linkages and to cross-ring cleavages.
Abstract: Simple Summary Glycosaminoglycans (GAGs) are considered to be the most difficult type of glycoconjugate to analyze as they are constituted of linear long polysaccharidic chains having molecular weights reaching up to several million daltons. Structural analysis of glycosaminoglycans from biological samples is a long and work-extensive procedure due to the many preparation steps involved. In addition, so far, only few research articles have been dedicated to the analysis of GAGs by means of matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) because their ionization can be problematic due to the presence of labile sulfate groups. In this work, we present an optimized strategy to analyze GAG disaccharides via MALDI-TOF mass spectrometry, using a fast workflow that does not require purification after enzymatic cleavage. For the first time, we show that it was possible to identify the sulfation position in disaccharides obtained from GAG via fragmentation experiments. This proof of concept is illustrated via the analysis of chondroitin/dermatan sulfate disaccharides of atherosclerotic lesions, in which we were able to identify their monosulfation patterns. Abstract Glycosaminoglycans (GAGs) are considered to be the most difficult type of glycoconjugates to analyze as they are constituted of linear long polysaccharidic chains having molecular weights reaching up to several million daltons. Bottom-up analysis of glycosaminoglycans from biological samples is a long and work-extensive procedure due to the many preparation steps involved. In addition, so far, only few research articles have been dedicated to the analysis of GAGs by means of matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF-MS) because their intact ionization can be problematic due to the presence of labile sulfate groups. In this work, we had the aim of exploring the sulfation pattern of monosulfated chondroitin/dermatan sulfate (CS/DS) disaccharides in human tissue samples because they represent the most abundant form of sulfation in disaccharides. We present here an optimized strategy to analyze on-target derivatized CS/DS disaccharides via MALDI-TOF-MS using a fast workflow that does not require any purification after enzymatic cleavage. For the first time, we show that MALDI-TOF/TOF experiments allow for discrimination between monosulfated CS disaccharide isomers via specific fragments corresponding to glycosidic linkages and to cross-ring cleavages. This proof of concept is illustrated via the analysis of CS/DS disaccharides of atherosclerotic lesions of different histological origins, in which we were able to identify their monosulfation patterns.
01 Jan 2010
TL;DR: The aim of this work is to investigate the spatial organization both in solutions of pure aggrecan and in solutions containing Aggrecan hyaluronic acid complexes.
Abstract: INTRODUCTION Aggrecan is a high molecular weight (1x10
Journal ArticleDOI
TL;DR: In this paper , the authors report the case of a 38-year-old woman with a history of joint restriction and retinitis pigmentosa who developed bivalvular heart failure requiring surgery.
Abstract: Mucopolysaccharidoses (MPS) are a group of inherited lysosomal storage disorders caused by deficient levels and/or activity of glycosaminoglycan (GAG)-degradative enzymes. MPS are characterized by accumulation of the mucopolysaccharides heparan sulfate, dermatan sulfate, keratan sulfate, or chondroitin sulfate in tissues. We report the case of a 38-year-old woman with a history of joint restriction and retinitis pigmentosa who developed bivalvular heart failure requiring surgery. It was not until pathological examination of surgically excised valvular tissue that a diagnosis of MPS I was made. Her musculoskeletal and ophthalmologic symptoms, when placed in the context of MPS I, painted the diagnostic picture of a genetic syndrome that was overlooked until a diagnosis was made in late middle age.
Book ChapterDOI
01 Jan 1989
TL;DR: The connective tissue is a target organ in the body, in which the dependent changes can be seen with the authors' eyes, and the wrinkling skin is one the evidences of the physiological ageing process.
Abstract: The connective tissue is a target organ in the body, in which the dependent changes can be seen with our eyes. The wrinkling skin is one the evidences of the physiological ageing process, especially of the connective tissue.
Patent
24 Dec 2009
TL;DR: In this article, a method for immunologically determining a keratan sulfate level which method includes bringing an anti-keratan sulfates monoclonal antibody into contact with a biological sample, exhibiting a relative reaction specificity between ksI and ksII represented by IC50 KS-I/KS-II of 0.4 to 5, to thereby provide a signal; and detecting ksion contained in the biological sample from the signal.
Abstract: The inventions provides a method for immunologically determining a keratan sulfate level which method includes bringing an anti-keratan sulfate monoclonal antibody into contact with a biological sample, the anti-keratan sulfate monoclonal antibody exhibiting a relative reaction specificity between keratan sulfate-I and keratan sulfate-II represented by IC50 KS-I/KS-II of 0.4 to 5, to thereby provide a signal; and detecting keratan sulfate contained in the biological sample from the signal. On the basis of the method, the invention also provides a joint disease detection method and a method for assessing the effect of a remedy for a joint disease and a candidate substance therefor. Through these methods, a very small amount of keratan sulfate contained in a sample, can be determined. Particularly, these methods can determine, at high-sensitivity and high-specificity, the total keratan sulfate including keratan sulfate-I, which have been difficult to determine through a conventional technique. The methods also enables detect a joint disease and assess the effect of a remedy for a joint disease or a candidate substance therefor.

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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
202310
202222
20217
20209
201912
201812