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一种具有芬太尼泛特异性的工程化人抗体片段,可逆转卡芬太尼引起的呼吸抑制。

An Engineered Human-Antibody Fragment with Fentanyl Pan-Specificity that Reverses Carfentanil-Induced Respiratory Depression.

作者信息

Eubanks Lisa M, Pholcharee Tossapol, Oyen David, Natori Yoshihiro, Zhou Bin, Wilson Ian A, Janda Kim D

机构信息

Departments of Chemistry and Immunology, The Scripps Research Institute, La Jolla, CA 92037, United States.

Department of Integrative Structural and Computational Biology, The Scripps Research Institute, La Jolla, CA 92037, United States.

出版信息

bioRxiv. 2023 Jul 4:2023.07.04.547721. doi: 10.1101/2023.07.04.547721.

Abstract

The opioid overdose crisis primarily driven by potent synthetic opioids resulted in more than 500,000 deaths in the US over the last 20 years. Though naloxone, a short acting medication, remains the primary treatment option for temporarily reversing opioid overdose effects, alternative countermeasures are needed. Monoclonal antibodies present a versatile therapeutic opportunity that can be tailored for synthetic opioids and that can help prevent post-treatment renarcotization. The ultrapotent analog carfentanil, is especially concerning due to its unique pharmacological properties. With this in mind, we generated a fully human antibody through a drug-specific B cell sorting strategy with a combination of carfentanil and fentanyl probes. The resulting pan-specific antibody was further optimized through scFv phage display. This antibody, C10-S66K, displays high affinity to carfentanil, fentanyl, and other analogs, and reversed carfentanil-induced respiratory depression. Additionally, x-ray crystal structures with carfentanil and fentanyl bound provided structural insight into key drug:antibody interactions.

摘要

由强效合成阿片类药物引发的阿片类药物过量危机在过去20年中导致美国超过50万人死亡。尽管纳洛酮这种短效药物仍然是暂时逆转阿片类药物过量影响的主要治疗选择,但仍需要其他对策。单克隆抗体提供了一种通用的治疗机会,可以针对合成阿片类药物进行定制,并有助于防止治疗后再次成瘾。超强效类似物卡芬太尼因其独特的药理特性而尤其令人担忧。考虑到这一点,我们通过结合卡芬太尼和芬太尼探针的药物特异性B细胞分选策略生成了一种全人源抗体。通过单链抗体噬菌体展示对所得的泛特异性抗体进行了进一步优化。这种抗体C10-S66K对卡芬太尼、芬太尼和其他类似物具有高亲和力,并逆转了卡芬太尼诱导的呼吸抑制。此外,与卡芬太尼和芬太尼结合的X射线晶体结构提供了对关键药物与抗体相互作用的结构见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b849/10349930/ccb2ab3ea124/nihpp-2023.07.04.547721v1-f0001.jpg

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