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评估蛋白质交联作为一种治疗策略,以稳定家族性肌萎缩侧索硬化症小鼠模型中的 SOD1 变异体。

Evaluating protein cross-linking as a therapeutic strategy to stabilize SOD1 variants in a mouse model of familial ALS.

机构信息

Department of Chemistry and Chemical Biology, Northeastern University, Boston, Massachusetts, United States of America.

Barnett Institute of Chemical and Biological Analysis, Boston, Massachusetts, United States of America.

出版信息

PLoS Biol. 2024 Jan 30;22(1):e3002462. doi: 10.1371/journal.pbio.3002462. eCollection 2024 Jan.

Abstract

Mutations in the gene encoding Cu-Zn superoxide dismutase 1 (SOD1) cause a subset of familial amyotrophic lateral sclerosis (fALS) cases. A shared effect of these mutations is that SOD1, which is normally a stable dimer, dissociates into toxic monomers that seed toxic aggregates. Considerable research effort has been devoted to developing compounds that stabilize the dimer of fALS SOD1 variants, but unfortunately, this has not yet resulted in a treatment. We hypothesized that cyclic thiosulfinate cross-linkers, which selectively target a rare, 2 cysteine-containing motif, can stabilize fALS-causing SOD1 variants in vivo. We created a library of chemically diverse cyclic thiosulfinates and determined structure-cross-linking-activity relationships. A pre-lead compound, "S-XL6," was selected based upon its cross-linking rate and drug-like properties. Co-crystallographic structure clearly establishes the binding of S-XL6 at Cys 111 bridging the monomers and stabilizing the SOD1 dimer. Biophysical studies reveal that the degree of stabilization afforded by S-XL6 (up to 24°C) is unprecedented for fALS, and to our knowledge, for any protein target of any kinetic stabilizer. Gene silencing and protein degrading therapeutic approaches require careful dose titration to balance the benefit of diminished fALS SOD1 expression with the toxic loss-of-enzymatic function. We show that S-XL6 does not share this liability because it rescues the activity of fALS SOD1 variants. No pharmacological agent has been proven to bind to SOD1 in vivo. Here, using a fALS mouse model, we demonstrate oral bioavailability; rapid engagement of SOD1G93A by S-XL6 that increases SOD1G93A's in vivo half-life; and that S-XL6 crosses the blood-brain barrier. S-XL6 demonstrated a degree of selectivity by avoiding off-target binding to plasma proteins. Taken together, our results indicate that cyclic thiosulfinate-mediated SOD1 stabilization should receive further attention as a potential therapeutic approach for fALS.

摘要

基因编码铜锌超氧化物歧化酶 1(SOD1)的突变导致一部分家族性肌萎缩侧索硬化症(fALS)病例。这些突变的一个共同作用是,正常情况下稳定的二聚体 SOD1 会解离成有毒的单体,从而引发有毒的聚集物。研究人员投入了大量精力开发能稳定 fALS SOD1 变体二聚体的化合物,但不幸的是,这尚未转化为治疗方法。我们假设,选择性靶向罕见的二硫键含 2 个半胱氨酸基序的环状硫代亚磺酸盐交联剂,可以稳定体内的 fALS 致病 SOD1 变体。我们创建了一个化学多样性的环状硫代亚磺酸盐文库,并确定了结构-交联-活性关系。根据其交联速率和类药性,选择了一个预先导化合物“ S-XL6”。共结晶结构清楚地确定了 S-XL6 在 Cys 111 处的结合,桥接单体并稳定 SOD1 二聚体。生物物理研究表明,S-XL6 提供的稳定性程度(高达 24°C)是前所未有的,据我们所知,对于任何动力学稳定剂的任何蛋白质靶标都是如此。基因沉默和蛋白质降解治疗方法需要仔细滴定剂量,以平衡减少 fALS SOD1 表达的益处与失去酶功能的毒性。我们表明,S-XL6 没有这种副作用,因为它可以挽救 fALS SOD1 变体的活性。没有药理学试剂被证明可以在体内与 SOD1 结合。在这里,我们使用 fALS 小鼠模型证明了口服生物利用度;S-XL6 快速与 SOD1G93A 结合,增加了 SOD1G93A 的体内半衰期;并且 S-XL6 可以穿过血脑屏障。S-XL6 通过避免与血浆蛋白的非靶标结合表现出一定程度的选择性。总之,我们的结果表明,环状硫代亚磺酸盐介导的 SOD1 稳定化应该作为治疗 fALS 的潜在方法得到进一步关注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9477/10826971/cdf2cf582a92/pbio.3002462.g001.jpg

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