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用于检测生物分子构象状态和酶活性的表面能量改性芯片。

Surface energy modified chips for detection of conformational states and enzymatic activity in biomolecules.

作者信息

Asberg Peter, Nilsson K Peter R, Inganäs Olle

机构信息

Biomolecular and Organic Electronics, IFM, Linköping University, S-581 83 Linköping, Sweden.

出版信息

Langmuir. 2006 Feb 28;22(5):2205-11. doi: 10.1021/la0527902.

Abstract

A novel patterning method for anchoring biomolecules and noncovalent assembled conjugated polyelectrolyte (CPE)/biomolecule complexes to a chip surface is presented. The surface energy of a hydrophilic substrate is modified using an elastomeric poly(dimethylsiloxane) (PDMS) stamp, containing a relief pattern. Modification takes place on the parts where the PDMS stamp is in conformal contact with the substrate and leaves low molecular weight PDMS residues on the surface resulting in a hydrophobic modification, and then biomolecules and CPE/biomolecule complexes are then adsorbed in a specific pattern. The method constitutes a discrimination system for different conformations in biomolecules using CPEs as reporters and the PDMS modified substrates as the discriminator. Detection of different conformations in two biomacromolecules, a synthetic peptide (JR2E) and a protein (calmodulin), reported by the CPE and resolved by fluorescence was demonstrated. Also, excellent enzyme activity in patterned CPE/horseradish peroxidase (HRP) enzyme was shown, demonstrating that this method can be used to pattern biomolecules with their activity retained. The method presented could be useful in various biochip applications, such as analyzing proteins and peptides in large-scale production, in making metabolic chips, and for making multi-microarrays.

摘要

本文提出了一种将生物分子以及非共价组装的共轭聚电解质(CPE)/生物分子复合物固定到芯片表面的新型图案化方法。使用含有浮雕图案的弹性聚二甲基硅氧烷(PDMS)印章对亲水性底物的表面能进行修饰。修饰发生在PDMS印章与底物共形接触的部分,并在表面留下低分子量的PDMS残留物,从而实现疏水修饰,然后生物分子和CPE/生物分子复合物以特定图案被吸附。该方法构成了一个区分系统,以CPE作为报告分子,以PDMS修饰的底物作为鉴别器,用于区分生物分子中的不同构象。通过荧光检测并证实了由CPE报告的两种生物大分子(一种合成肽(JR2E)和一种蛋白质(钙调蛋白))中的不同构象。此外,还展示了图案化的CPE/辣根过氧化物酶(HRP)酶具有优异的酶活性,表明该方法可用于对具有保留活性的生物分子进行图案化。所提出的方法在各种生物芯片应用中可能有用,例如大规模生产中分析蛋白质和肽、制造代谢芯片以及制造多微阵列。

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