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用于分离肽 - 寡核苷酸缀合物的高分辨率高效液相色谱法。

High-Resolution HPLC for Separating Peptide-Oligonucleotide Conjugates.

作者信息

Naganuma Miyako, Tsuji Genichiro, Amiya Misato, Hirai Reira, Higuchi Yuki, Hata Naoko, Nozawa Saoko, Watanabe Daishi, Nakajima Taeko, Demizu Yosuke

机构信息

Division of Organic Chemistry, National Institute of Health Sciences, 3-25-26 Tonomachi, Kawasaki-ku, Kawasaki-shi, Kanagawa 210-9501, Japan.

Graduate School of Medical Life Science, Yokohama City University, 1-7-29, Suehiro-cho, Tsurumi-ku, Yokohama-shi, Kanagawa 230-0045, Japan.

出版信息

ACS Omega. 2025 Apr 30;10(20):20578-20584. doi: 10.1021/acsomega.5c01308. eCollection 2025 May 27.

Abstract

Peptide-oligonucleotide conjugates (POCs) are chimeric molecules that combine the specificity of oligonucleotides with the functionality of peptides, improving the delivery and therapeutic potential of nucleic acid-based drugs. However, the analysis of POCs, particularly those containing arginine-rich sequences, poses major challenges because of aggregation caused by electrostatic interactions. In this study, we developed an optimized high-performance liquid chromatography (HPLC) method for analyzing POCs. Using a conjugate of DNA and nona-arginine as a model compound, we systematically investigated the effects of various analytical parameters, including column type, column temperature, mobile-phase composition, and pH. A column packed with C18 resin with wide pores combined with butylammonium acetate as the ion-pairing reagent and an optimal column temperature of 80 °C provided superior peak resolution and sensitivity. The optimized conditions gave clear separation of POCs from unlinked oligonucleotides and enabled the detection of nucleic acid fragments lacking an alkyne moiety as a linkage part, which is critical for quality control. Our HPLC method is robust and reproducible and substantially reduces the complexity, time, and cost associated with the POC analysis. The method may improve the efficiency of quality control in the production of POCs, thereby supporting their development as promising therapeutic agents for clinical applications.

摘要

肽 - 寡核苷酸缀合物(POCs)是一种嵌合分子,它将寡核苷酸的特异性与肽的功能相结合,提高了基于核酸的药物的递送和治疗潜力。然而,POCs的分析,尤其是那些含有富含精氨酸序列的POCs,由于静电相互作用导致的聚集而带来了重大挑战。在本研究中,我们开发了一种优化的高效液相色谱(HPLC)方法用于分析POCs。以DNA与九聚精氨酸的缀合物作为模型化合物,我们系统地研究了各种分析参数的影响,包括柱类型、柱温、流动相组成和pH值。填充有宽孔C18树脂的色谱柱与乙酸丁铵作为离子对试剂相结合,以及80°C的最佳柱温,提供了优异的峰分辨率和灵敏度。优化后的条件能够清晰地将POCs与未连接的寡核苷酸分离,并能够检测缺少作为连接部分的炔基部分的核酸片段,这对于质量控制至关重要。我们的HPLC方法稳健且可重复,大大降低了与POC分析相关的复杂性、时间和成本。该方法可能会提高POCs生产中的质量控制效率,从而支持它们作为有前景的临床应用治疗剂的开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a8/12120573/e52e8dc3270d/ao5c01308_0001.jpg

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