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Enzyme Accessibility and Solid Supports: Which Molecular Weight Enzymes Can Be Used on Solid Supports? An Investigation Using Confocal Raman Microscopy

机译:酶的可及性和固体支持物:哪些分子量的酶可以用于固体支持物?使用共焦拉曼显微镜进行调查

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摘要

The accessibility of various solid supports (TentaGel, PEGA 1900, and beaded controlled pore glasses (CPGs)) to a range of enzymes was investigated. The different beaded materials were loaded with the peptide 4-cyanobenzamide-Gly-Pro-Leu-Gly-Leu-Phe-Ala-Arg-OH and incubated with the enzymes MMP-12 (22 kDa), thermolysin (35 kDa), MMP-13 (42.5 kDa), clostridium collagenase (68 kDa), and NEP (90 kDa). The absence/presence of the cyano stretching frequency was measured by means of confocal Raman microscopy. It was found that none of the investigated enzymes could enter the polymer matrices of TentaGel. PEGA 1900 was compatible only with the two smallest enzymes, while beaded CPG was successful even with NEP (90 kDa), proving its superiority over other materials in terms of bio-compatibility.
机译:研究了各种固体支持物(TentaGel,PEGA 1900和串珠控制孔玻璃(CPG))对各种酶的可及性。在不同的串珠材料中加载肽4-cyanobenzamide-Gly-Pro-Leu-Gly-Leu-Phe-Ala-Arg-OH,并与酶MMP-12(22 kDa),嗜热菌蛋白酶(35 kDa),MMP一起孵育-13(42.5 kDa),梭菌胶原酶(68 kDa)和NEP(90 kDa)。通过共焦拉曼显微镜测量氰基拉伸频率的存在/不存在。发现所研究的酶均不能进入TentaGel的聚合物基质。 PEGA 1900仅与两种最小的酶相容,而串珠CPG即使在NEP(90 kDa)的情况下也很成功,证明了其在生物相容性方面优于其他材料的优越性。

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