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锰离子与锤头状核酶结合亲和力的电子顺磁共振光谱测量及其与切割活性的相关性。

Electron paramagnetic resonance spectroscopic measurement of Mn2+ binding affinities to the hammerhead ribozyme and correlation with cleavage activity.

作者信息

Horton T E, Clardy D R, DeRose V J

机构信息

Department of Chemistry, Texas A&M University, College Station 77842-3012, USA.

出版信息

Biochemistry. 1998 Dec 22;37(51):18094-101. doi: 10.1021/bi981425p.

Abstract

Efficient phosphodiester bond cleavage activity by the hammerhead ribozyme requires divalent cations. Toward understanding this metal ion requirement, the Mn2+-binding properties of hammerhead model ribozymes have been investigated under dilute solution conditions, using electron paramagnetic resonance spectroscopy (EPR) to detect free Mn2+ in the presence of added ribozyme. Numbers and affinities of bound Mn2+ were obtained at pH 7.8 (5 mM triethanolamine) in the presence of 0, 0.1, and 1.0 M NaCl for an RNA-DNA model consisting of a 13-nucleotide DNA "substrate" hybridized to a 34-nucleotide RNA "enzyme" [Pley, H. W., Flaherty, K. M., and McKay, D. B. (1994) Nature 372, 68-74]. In 0.1 M NaCl, two classes of Mn2+ sites are found with n1 = 3.7 +/- 0.4, Kd(1) = 4 +/- 1 microM (type 1) and n2 = 5.2 +/- 0.4, Kd(2) = 460 +/- 130 microM (type 2). The high-affinity type 1 sites are confirmed for an active RNA-RNA hybrid (34-nucleotide RNA enzyme:13-nucleotide RNA substrate) by EPR measurements at low Mn2+ concentrations. Decreasing NaCl concentration results in an increased number of bound Mn2+ per hammerhead. By contrast, a binding titration in 1 M NaCl indicates that a single Mn2+ site with apparent Kd approximately 10 microM is populated in low concentrations of Mn2+, and apparent cooperative effects at higher Mn2+ concentrations result in population of a similar total number of Mn2+ sites (n1 = 8-10) as found in 0.1 M NaCl. Mn2+-dependent activity profiles are similar for the active RNA-RNA hybrid in 0.1 and 1 M NaCl. Correlation with binding affinities determined by EPR indicates that hammerhead activity in 0.1 M NaCl is only observed after all four of the high-affinity Mn2+ sites are occupied, rises with population of the type 2 sites, and is independent of Mn2+ concentrations corresponding to > 8-9 Mn2+ bound per hammerhead. Equivalent measurements in 1 M NaCl demonstrate a rise in activity with the cooperative transition observed in the Mn2+ binding curve. These measurements indicate that, over this NaCl concentration range, hammerhead ribozyme activity is influenced by population of a specific set of divalent cation sites.

摘要

锤头状核酶高效的磷酸二酯键切割活性需要二价阳离子。为了理解这种对金属离子的需求,在稀溶液条件下研究了锤头状模型核酶的Mn2+结合特性,使用电子顺磁共振光谱(EPR)在添加核酶的情况下检测游离的Mn2+。对于由一个13个核苷酸的DNA“底物”与一个34个核苷酸的RNA“酶”杂交而成的RNA-DNA模型,在pH 7.8(5 mM三乙醇胺)、存在0、0.1和1.0 M NaCl的条件下获得了结合的Mn2+的数量和亲和力[Pley, H. W., Flaherty, K. M., and McKay, D. B. (1994) Nature 372, 68 - 74]。在0.1 M NaCl中,发现两类Mn2+位点,n1 = 3.7 ± 0.4,Kd(1) = 4 ± 1 μM(1型),n2 = 5.2 ± 0.4,Kd(2) = 460 ± 130 μM(2型)。通过在低Mn2+浓度下的EPR测量,证实了活性RNA-RNA杂交体(34个核苷酸的RNA酶:13个核苷酸的RNA底物)存在高亲和力的1型位点。降低NaCl浓度会导致每个锤头状结构结合的Mn2+数量增加。相比之下,在1 M NaCl中的结合滴定表明,在低浓度的Mn2+下存在一个表观Kd约为10 μM的单一Mn2+位点,在较高Mn2+浓度下的表观协同效应导致与在0.1 M NaCl中发现的Mn2+位点总数(n1 = 8 - 10)相似的数量。在0.1和1 M NaCl中,活性RNA-RNA杂交体的Mn2+依赖性活性曲线相似。与EPR测定的结合亲和力的相关性表明,在0.1 M NaCl中,只有在所有四个高亲和力的Mn2+位点都被占据后才观察到锤头状活性,随着2型位点的占据而增加,并且与每个锤头状结构结合> 8 - 9个Mn2+对应的Mn2+浓度无关。在1 M NaCl中的等效测量表明,活性随着在Mn2+结合曲线中观察到的协同转变而增加。这些测量表明,在这个NaCl浓度范围内,锤头状核酶的活性受到特定一组二价阳离子位点占据情况的影响。

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