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病毒DNA和蛋白质成分的紫外共振拉曼光谱:257、244、238和229纳米激发下的归属和截面

UV resonance Raman spectroscopy of DNA and protein constituents of viruses: assignments and cross sections for excitations at 257, 244, 238, and 229 nm.

作者信息

Wen Z Q, Thomas G J

机构信息

Division of Cell Biology and Biophysics, School of Biological Sciences, University of Missouri, Kansas City 64110, USA.

出版信息

Biopolymers. 1998 Mar;45(3):247-56. doi: 10.1002/(SICI)1097-0282(199803)45:3<247::AID-BIP7>3.0.CO;2-R.

Abstract

Ultraviolet resonance Raman (UVRR) spectra of H2O and D2O solutions of the nucleoside (dA, dG, dC, dT) and aromatic amino acid (Phe, Trp, Tyr) constituents of DNA viruses have been obtained with laser excitation wavelengths of 257, 244, 238, and 229 nm. Using the 981 cm-1 marker of Na2SO4 as an internal standard, Raman frequencies and scattering cross sections were evaluated for all prominent UVRR bands at each excitation wavelength. The results show that UVRR cross sections of both the nucleosides and amino acids are strongly dependent on excitation wavelength and constitute sensitive and selective probes of the residues. The results provide a library of UVRR marker bands for structural analysis of DNA viruses and other nucleoprotein assemblies.

摘要

已使用257、244、238和229nm的激光激发波长获得了DNA病毒的核苷(dA、dG、dC、dT)和芳香族氨基酸(Phe、Trp、Tyr)成分的H2O和D2O溶液的紫外共振拉曼(UVRR)光谱。以Na2SO4的981cm-1标记作为内标,对每个激发波长下所有突出的UVRR谱带的拉曼频率和散射截面进行了评估。结果表明,核苷和氨基酸的UVRR截面都强烈依赖于激发波长,并且构成了对这些残基敏感且具有选择性的探针。这些结果为DNA病毒和其他核蛋白组装体的结构分析提供了一个UVRR标记谱带库。

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