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钆离子振动边带光谱学。应用于生物大分子的钙离子结合位点的新型光学探针。

Gd3+ vibronic side band spectroscopy. New optical probe of Ca2+ binding sites applied to biological macromolecules.

作者信息

Iben I E, Stavola M, Macgregor R B, Zhang X Y, Friedman J M

机构信息

Chemistry Department, New York University, New York 10003.

出版信息

Biophys J. 1991 May;59(5):1040-9. doi: 10.1016/S0006-3495(91)82319-0.

Abstract

A new spectroscopic technique is presented for obtaining infraredlike spectra of the binding sites of Ca2+ and other metals in biological macromolecules. The technique, based on the Ca(2+)-like binding properties of Gd3+, utilizes vibronic side bands (VSB) that appear in Gd3+ fluorescence. In the fluorescence spectrum of Gd3+, the separation in photon frequency between a VSB and its electronic origin at approximately 32,150 cm-1 (approximately 311 nm) is a direct measure of the vibrational frequency of a ligand coordinated to Gd3+ ion. As a consequence, the VSB are uncomplicated by molecular vibrations distant from the Gd3+ binding site. The vibrational spectra resulting from the VSB of Gd3+ coordinated to a Ca2+ binding protein, a phospholipid, and DNA are presented.

摘要

本文介绍了一种新的光谱技术,用于获取生物大分子中Ca2+和其他金属结合位点的类红外光谱。该技术基于Gd3+的类Ca(2+)结合特性,利用Gd3+荧光中出现的振动边带(VSB)。在Gd3+的荧光光谱中,VSB与其电子起源(约32,150 cm-1,约311 nm)之间的光子频率间隔是与Gd3+离子配位的配体振动频率的直接量度。因此,VSB不受远离Gd3+结合位点的分子振动的干扰。文中展示了与Ca2+结合蛋白、磷脂和DNA配位的Gd3+的VSB所产生的振动光谱。

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本文引用的文献

1
Glassy behavior of a protein.蛋白质的玻璃态行为。
Phys Rev Lett. 1989 Apr 17;62(16):1916-1919. doi: 10.1103/PhysRevLett.62.1916.
5
Structure and evolution of calcium-modulated proteins.钙调节蛋白的结构与进化
CRC Crit Rev Biochem. 1980;8(2):119-74. doi: 10.3109/10409238009105467.
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Double helix at atomic resolution.原子分辨率下的双螺旋结构。
Nature. 1973 May 18;243(5403):150-4. doi: 10.1038/243150a0.
9
Hydration of proteins and polypeptides.蛋白质和多肽的水合作用。
Adv Protein Chem. 1974;28:239-345. doi: 10.1016/s0065-3233(08)60232-6.

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