Schiff L A, Nibert M L, Fields B N
Department of Microbiology and Molecular Genetics, Harvard Medical School, Boston, MA.
Proc Natl Acad Sci U S A. 1988 Jun;85(12):4195-9. doi: 10.1073/pnas.85.12.4195.
We have characterized a simple method that uses 65ZnCl2 to detect zinc-binding proteins that have been immobilized on nitrocellulose. Conditions have been identified that permit the detection of as little as 1 microgram of some zinc-binding proteins. The specificity of the binding is indicated by the ability of other divalent metal ions to compete with 65Zn(II) in this assay. We have used this technique to provide evidence that the nucleic acid-binding gag protein of retroviruses also binds zinc. This technique can be applied to biological mixtures of proteins and may be used in proteolytic mapping studies to identify protein fragments that have zinc-binding activity.
我们已经描述了一种简单的方法,该方法使用氯化锌65来检测固定在硝酸纤维素上的锌结合蛋白。已经确定了一些条件,这些条件能够检测低至1微克的某些锌结合蛋白。在该检测中,其他二价金属离子与锌65(II)竞争的能力表明了结合的特异性。我们已经使用该技术来证明逆转录病毒的核酸结合gag蛋白也能结合锌。该技术可应用于蛋白质的生物混合物,并且可用于蛋白水解图谱研究,以鉴定具有锌结合活性的蛋白质片段。