Iben I E, Stavola M, Macgregor R B, Zhang X Y, Friedman J M
Chemistry Department, New York University, New York 10003.
Biophys J. 1991 May;59(5):1040-9. doi: 10.1016/S0006-3495(91)82319-0.
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.
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。