Understanding enzyme action on immobilised substrates

被引:51
作者
Halling, PJ [1 ]
Ulijn, RV
Flitsch, SL
机构
[1] Univ Strathclyde, Dept Pure & Appl Chem, Glasgow G1 1XW, Lanark, Scotland
[2] Univ Manchester, Sch Mat, Manchester M1 7HS, Lancs, England
[3] Univ Manchester, Sch Chem, Manchester M1 7HS, Lancs, England
关键词
D O I
10.1016/j.copbio.2005.06.006
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
With increasing interest in automated synthesis and screening protocols, solid supported chemistry and biochemistry are attractive technologies. Studies with surface-immobilised substrates have been carried out to analyse enzyme accessibility, kinetics and thermodynamics. Several interesting new methods have been developed to monitor enzyme action on substrates attached to a solid phase such as polymer beads glass or gold surfaces. These include fluorescence measurements, MALDI-TOF mass spectrometry, and the use of quartz crystal microbalances to measure weight changes of immobilised molecules directly on the surface. Approaches that allow spatial resolution in single beads have also been reported. The ability of enzymes to reach the inside of beads is becoming better characterised and new supports have been developed that allow improved accessibility. The equilibrium position of reactions on the solid surface can be substantially shifted compared with reactions in solution, and this can be usefully exploited using hydrolases in reverse. Research is also starting to tackle the way in which kinetics are modified when the substrates are surface immobilised.
引用
收藏
页码:385 / 392
页数:8
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