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拉姆达θ反射测量法:一种测量平面蛋白质阵列中光学薄膜厚度的新技术。

Lambda Theta Reflectometry: A New Technique for Measuring Optical Film Thickness in Planar Protein Arrays.

作者信息

Klose Alanna M, Katz Joseph D, Boni Robert, Nelson David, Hassard Brian, Miller Benjamin L

机构信息

Department of Dermatology, University of Rochester, Rochester, New York 14627, United States.

Materials Science Program, University of Rochester, Rochester, New York 14627, United States.

出版信息

ACS Sens. 2025 Jul 25;10(7):5097-5107. doi: 10.1021/acssensors.5c01108. Epub 2025 Jul 2.

Abstract

Quantitative protein measurements provide valuable information about biological pathways, immune system functionality, and the mechanisms of disease. The most accurate methods for detecting proteins are label-free and preserve native protein-binding interactions. Label-free biomolecular interaction analysis includes reflectometry, a group of techniques that detect proteins by measuring the reflectance properties of a thin film on a substrate. Most of these techniques are limited in some way by instrument complexity, sensitivity, or consumable manufacturing requirements. To address these issues, we introduce Lambda Theta Reflectometry (LTR), a new reflectometric technique that measures changes in film thickness by determining the point of null reflectivity as a function of wavelength (lambda) and angle of incidence (theta). The substrate is simultaneously illuminated with a range of angles and wavelengths, and reflected light is resolved both angularly and spectrally. Our prototype LTR reflectometer can measure SiO layer thickness with milli-Ångström precision. LTR measurements of Si/SiO oxide films are in excellent agreement with spectroscopic ellipsometry for film thicknesses ranging from 1390 to 1465 Å. This technique enables label-free biosensing measurements across a range of biological analyte concentrations (0.5 ng/mL to μg/mL) without requiring stringent control over probe deposition thickness or substrate manufacturing.

摘要

蛋白质定量测量可提供有关生物途径、免疫系统功能和疾病机制的宝贵信息。检测蛋白质最准确的方法是无标记法,该方法能保留天然蛋白质结合相互作用。无标记生物分子相互作用分析包括反射测量法,这是一组通过测量底物上薄膜的反射特性来检测蛋白质的技术。这些技术大多在某种程度上受到仪器复杂性、灵敏度或耗材制造要求的限制。为解决这些问题,我们引入了拉姆达-西塔反射测量法(LTR),这是一种新的反射测量技术,它通过确定零反射率点作为波长(拉姆达)和入射角(西塔)的函数来测量薄膜厚度的变化。用一系列角度和波长同时照射底物,反射光在角度和光谱上都得到解析。我们的LTR反射仪原型能够以毫埃精度测量SiO层厚度。对于厚度在1390至1465埃范围内的Si/SiO氧化膜,LTR测量结果与椭圆偏振光谱法的测量结果非常吻合。该技术能够在一系列生物分析物浓度(0.5纳克/毫升至微克/毫升)范围内进行无标记生物传感测量,而无需对探针沉积厚度或底物制造进行严格控制。

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