High-throughput functional assessment of polysaccharide-active enzymes using matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry as exemplified on plant cell wall polysaccharides

被引:11
作者
Leboeuf, Edouard [2 ]
Immerzeel, Peter [3 ]
Gibon, Yves [3 ]
Steup, Martin [2 ]
Pauly, Markus [1 ]
机构
[1] Michigan State Univ, MSU DOE Plant Res Lab, E Lansing, MI 48824 USA
[2] Univ Potsdam, Inst Biochem & Biol, Dept Plant Physiol, D-14476 Potsdam, Germany
[3] Max Planck Inst Mol Plant Physiol, D-14476 Potsdam, Germany
关键词
glycosyltransferase; esterase; substrate specificity; MALDI-TOF mass spectrometry;
D O I
10.1016/j.ab.2007.10.007
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Despite a wealth of sequence information on genes encoding carbohydrate-active enzymes (e.g., transferases, esterases, hydrolases), very few of these enzymes have been described in detail, particularly regarding substrate specificities. A facile and rapid method for the characterization of substrate specificities of polysaccharide-active enzymes that uses matrix-assisted laser desorption-time of flight mass spectrometry (MALDI-TOF MS) has been developed. This method has been applied to characterize a xyloglucan fucosyltransferase and a pectin methyl-esterase. Reactions were performed in liquid phase, and aliquots of the reaction mixtures were spotted on a polyvinylidene fluoride (PVDF) membrane. Reaction products were precipitated onto the membrane and cleaned by treatment with an ethanol-water mixture. Subsequently, the reaction products were hydrolyzed by specific endoglycanases, and the resulting oligosaccharides were directly analyzed onto the PVDF membrane by MALDI-TOF MS. The new method is amenable to high-throughput analysis and, thus, constitutes an emerging avenue to rapidly fill the gap in our knowledge of the specificities of polysaccharide-active enzymes. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:9 / 17
页数:9
相关论文
共 28 条
[1]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[2]   High-throughput identification of fucosyltransferase inhibitors using carbohydrate microarrays [J].
Bryan, MC ;
Lee, LV ;
Wong, CH .
BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2004, 14 (12) :3185-3188
[3]   Practical quantitative biomedical applications of MALDI-TOF mass spectrometry [J].
Bucknall, M ;
Fung, KYC ;
Duncan, MW .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2002, 13 (09) :1015-1027
[4]   Quantitative matrix-assisted laser desorption/ionization mass spectrometry for the determination of enzyme activities [J].
Bungert, D ;
Heinzle, E ;
Tholey, A .
ANALYTICAL BIOCHEMISTRY, 2004, 326 (02) :167-175
[5]  
Coutinho PM, 1999, ROY SOC CH, P3
[6]   A complementary bioinformatics approach to identify potential plant cell wall glycosyltransferase-encoding genes [J].
Egelund, J ;
Skjot, M ;
Geshi, N ;
Ulvskov, P ;
Petersen, BL .
PLANT PHYSIOLOGY, 2004, 136 (01) :2609-2620
[7]   Proton-activated fluorescence as a tool for simultaneous screening of combinatorial chemical reactions [J].
Evans, CA ;
Miller, SJ .
CURRENT OPINION IN CHEMICAL BIOLOGY, 2002, 6 (03) :333-338
[8]   Technological advances in high-throughput screening [J].
Fernandes, PB .
CURRENT OPINION IN CHEMICAL BIOLOGY, 1998, 2 (05) :597-603
[9]   Intracellular detection assays for high-throughput screening [J].
González, JE ;
Negulescu, PA .
CURRENT OPINION IN BIOTECHNOLOGY, 1998, 9 (06) :624-631
[10]   ADAPTATION OF THE NELSON-SOMOGYI REDUCING-SUGAR ASSAY TO A MICROASSAY USING MICROTITER PLATES [J].
GREEN, F ;
CLAUSEN, CA ;
HIGHLEY, TL .
ANALYTICAL BIOCHEMISTRY, 1989, 182 (02) :197-199