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溶液中和光热加热凝胶中多层金纳米粒子辅助的蛋白质胰酶消化。

Multilayer gold nanoparticle-assisted protein tryptic digestion in solution and in gel under photothermal heating.

机构信息

Department of Applied Chemistry, National Chiao Tung University, Hsinchu 300, Taiwan.

出版信息

Anal Bioanal Chem. 2011 Jan;399(1):377-85. doi: 10.1007/s00216-010-4375-3. Epub 2010 Nov 8.

Abstract

Elevating the reaction temperature is an effective method to accelerate protein enzymatic digestion because it can promote protein denaturation and enzyme activities. In this study, we demonstrated a new photothermal heating method to assist protein tryptic digestion on glass slides. A glass slide coated with layer-by-layer gold nanoparticles (Glass@AuNPs), combined with the use of a near infrared (NIR) diode laser, was used to raise reaction temperature during tryptic digestion in a short period of time. The modified glass slide is capable of absorbing NIR light arising from the dipole-dipole interactions between Au NPs immobilized on the slide. The temperature of Glass@AuNPs rapidly increased when irradiated by the NIR laser, accelerating protein enzymatic digestion conducted on the slide. Thus, when performing the tryptic digestion of proteins on the Glass@AuNPs slide under NIR irradiation, 3.5 min was sufficient to carry out the tryptic digestion of proteins in solution, while less than 5 min was adequate for in-gel tryptic digestion of proteins. Matrix-assisted laser desorption/ionization mass spectrometry was used for characterization of the tryptic digestion product. On the basis of the results, the time taken to analyze proteins could be greatly reduced using this current approach.

摘要

提高反应温度是加速蛋白质酶解的有效方法,因为它可以促进蛋白质变性和酶活性。在这项研究中,我们展示了一种新的光热加热方法,以辅助玻璃载玻片上的蛋白质胰蛋白酶消化。通过层层包裹金纳米粒子(Glass@AuNPs)对玻璃载玻片进行修饰,结合近红外(NIR)二极管激光的使用,可以在短时间内提高胰蛋白酶消化过程中的反应温度。修饰后的玻璃载玻片能够吸收由于固定在载玻片上的 Au NPs 之间的偶极-偶极相互作用而产生的近红外光。当用 NIR 激光照射时,Glass@AuNPs 的温度迅速升高,加速了载玻片上的蛋白质酶解。因此,当在 NIR 照射下在 Glass@AuNPs 载玻片上进行蛋白质胰蛋白酶消化时,3.5 分钟足以完成溶液中蛋白质的胰蛋白酶消化,而不到 5 分钟即可完成蛋白质的胶内胰蛋白酶消化。基质辅助激光解吸/电离质谱用于胰蛋白酶消化产物的表征。基于这些结果,使用当前方法可以大大缩短分析蛋白质所需的时间。

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