Kumar Srividya, Verma Taru, Mukherjee Ria, Ariese Freek, Somasundaram Kumaravel, Umapathy Siva
Department of Inorganic and Physical Chemistry, Indian Institute of Science, Bengaluru 560 012, India.
Centre for Biosystems Science and Engineering, Indian Institute of Science, Bangalore-560012, India.
Chem Soc Rev. 2016 Apr 7;45(7):1879-900. doi: 10.1039/c5cs00540j.
Biomolecular structure elucidation is one of the major techniques for studying the basic processes of life. These processes get modulated, hindered or altered due to various causes like diseases, which is why biomolecular analysis and imaging play an important role in diagnosis, treatment prognosis and monitoring. Vibrational spectroscopy (IR and Raman), which is a molecular bond specific technique, can assist the researcher in chemical structure interpretation. Based on the combination with microscopy, vibrational microspectroscopy is currently emerging as an important tool for biomedical research, with a spatial resolution at the cellular and sub-cellular level. These techniques offer various advantages, enabling label-free, biomolecular fingerprinting in the native state. However, the complexity involved in deciphering the required information from a spectrum hampered their entry into the clinic. Today with the advent of automated algorithms, vibrational microspectroscopy excels in the field of spectropathology. However, researchers should be aware of how quantification based on absolute band intensities may be affected by instrumental parameters, sample thickness, water content, substrate backgrounds and other possible artefacts. In this review these practical issues and their effects on the quantification of biomolecules will be discussed in detail. In many cases ratiometric analysis can help to circumvent these problems and enable the quantitative study of biological samples, including ratiometric imaging in 1D, 2D and 3D. We provide an extensive overview from the recent scientific literature on IR and Raman band ratios used for studying biological systems and for disease diagnosis and treatment prognosis.
生物分子结构解析是研究生命基本过程的主要技术之一。由于疾病等各种原因,这些过程会受到调节、阻碍或改变,这就是生物分子分析和成像在诊断、治疗预后和监测中发挥重要作用的原因。振动光谱(红外和拉曼)是一种分子键特异性技术,可以帮助研究人员进行化学结构解析。基于与显微镜的结合,振动显微光谱目前正在成为生物医学研究的一种重要工具,具有细胞和亚细胞水平的空间分辨率。这些技术具有多种优势,能够在天然状态下进行无标记的生物分子指纹识别。然而,从光谱中解读所需信息的复杂性阻碍了它们进入临床应用。如今,随着自动化算法的出现,振动显微光谱在光谱病理学领域表现出色。然而,研究人员应该意识到基于绝对谱带强度的定量分析可能会受到仪器参数、样品厚度、含水量、底物背景和其他可能的假象的影响。在这篇综述中,将详细讨论这些实际问题及其对生物分子定量分析的影响。在许多情况下,比率分析可以帮助规避这些问题,并实现对生物样品的定量研究,包括一维、二维和三维的比率成像。我们从最近的科学文献中提供了关于用于研究生物系统以及疾病诊断和治疗预后的红外和拉曼谱带比率的广泛概述。