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多功能且非破坏性的生物分子固定化光化学过程。

Versatile and nondestructive photochemical process for biomolecule immobilization.

机构信息

CEA, IRAMIS, SPCSI Chemistry of Surfaces and Interfaces Group, F-91191 Gif-sur-Yvette, France.

出版信息

Langmuir. 2013 Feb 12;29(6):2075-82. doi: 10.1021/la304941a. Epub 2013 Jan 30.

Abstract

Covalent immobilization of unmodified biological materials as proteins has been performed through a one-step and soft method. This process is based on a polyazidophenylene layer derived from the electroreduction of the parent salt 4-azidobenzenediazonium tetrafluoborate on gold substrates. The wavelength used (365 nm) for the photochemical grafting of a large variety of molecules as biomolecules is a key point to this nondestructive immobilization method. This simple process is also versatile and could be used for covalently binding a wide range of molecules such as polyethylene glycol moieties, for example. To validate this approach for biochip or microarray fabrication, a surface plasmon resonance imaging (SPRi) platform for immobilization of various antibody families was created by grafting G-protein through this process. This SPRi antibodies platform was tested with several consecutive cycles of antigen injections/regeneration steps without loss of activity.

摘要

通过一步软化学方法实现了对未经修饰的生物材料(如蛋白质)的共价固定化。该过程基于母体盐 4-叠氮苯重氮四氟硼酸盐在金基底上电化学还原得到的聚叠氮苯层。用于光化学接枝各种分子(如生物分子)的波长(365nm)是这种非破坏性固定化方法的关键。这种简单的方法也具有多功能性,可以用于共价结合各种分子,例如聚乙二醇部分。为了验证该方法在生物芯片或微阵列制造中的适用性,通过该过程接枝 G 蛋白,创建了用于固定各种抗体家族的表面等离子体共振成像(SPRi)平台。该 SPRi 抗体平台在多次连续的抗原注射/再生步骤中进行了测试,没有活性损失。

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