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一篇关于将 Ga 用作生物无机模型研究中 Fe 的替代物的观点文章及其在治疗用途中的成功应用。

A perspective essay on the use of Ga as a proxy for Fe in bioinorganic model studies and its successful use for therapeutic purposes.

机构信息

Duke University Department of Chemistry, Durham, NC 27708-0346, USA.

Department of Chemistry, East Carolina University, Greenville, NC 27858, USA.

出版信息

J Inorg Biochem. 2021 Jun;219:111411. doi: 10.1016/j.jinorgbio.2021.111411. Epub 2021 Mar 20.

Abstract

The use of Ga as a structural mimic for Fe in model bioinorganic investigations is usually based on a common assumption that Ga and Fe should form bioligand complexes of similar stabilities due to their similar charge/radius ratio (z/r). However, the literature survey presented here is contrary to this notion, showing that under laboratory conditions often Ga forms weaker bioligand complexes than Fein aqueous medium. We hypothesize that this is because Ga is more aquaphilic than Fe as suggested by their relative heats of hydration (ΔH). The successful use of Ga as a therapeutic agent is also briefly reviewed, showing this success often stems from the redox inertness as well as different pharmacokinetics of Ga than Fe, but similar metabolic pathways as Fe in human serum.

摘要

在模型生物无机研究中,使用 Ga 作为 Fe 的结构模拟物通常基于一个常见的假设,即由于 Ga 和 Fe 的电荷/半径比(z/r)相似,它们应该形成具有相似稳定性的生物配体络合物。然而,这里呈现的文献调查与这一概念相反,表明在实验室条件下,Ga 通常比 Fe 在水相介质中形成更弱的生物配体络合物。我们假设这是因为 Ga 比 Fe 更亲水,正如它们的相对水合热(ΔH)所表明的那样。Ga 作为治疗剂的成功应用也被简要回顾,表明这种成功通常源于 Ga 的氧化还原惰性以及 Ga 在人类血清中的药代动力学与 Fe 不同,但代谢途径与 Fe 相似。

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