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靶向生物缀合与核医学成像。

Site-specific bioconjugation and nuclear imaging.

机构信息

Department of Chemistry, Hunter College, City University of New York, New York, NY, USA; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Ph.D. Program in Biochemistry, Graduate Center of City University of New York, New York, NY, USA.

Department of Chemistry, Hunter College, City University of New York, New York, NY, USA; Department of Radiology, Memorial Sloan Kettering Cancer Center, New York, NY, USA; Ph.D. Program in Chemistry, Graduate Center of City University of New York, New York, NY, USA.

出版信息

Curr Opin Chem Biol. 2024 Aug;81:102471. doi: 10.1016/j.cbpa.2024.102471. Epub 2024 Jun 3.

DOI:10.1016/j.cbpa.2024.102471
PMID:38833913
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11323144/
Abstract

Monoclonal antibodies and antibody fragments have proven to be highly effective vectors for the delivery of radionuclides to target tissues for positron emission tomography (PET) and single-photon emission computed tomography (SPECT). However, the stochastic methods that have traditionally been used to attach radioisotopes to these biomolecules inevitably produce poorly defined and heterogeneous probes and can impair the ability of the immunoglobulins to bind their molecular targets. In response to this challenge, an array of innovative site-specific and site-selective bioconjugation strategies have been developed, and these approaches have repeatedly been shown to yield better-defined and more homogeneous radioimmunoconjugates with superior in vivo performance than their randomly modified progenitors. In this Current Opinion in Chemical Biology review, we will examine recent advances in this field, including the development - and, in some cases, clinical translation - of nuclear imaging agents radiolabeled using strategies that target the heavy chain glycans, peptide tags, and unnatural amino acids.

摘要

单克隆抗体和抗体片段已被证明是将放射性核素递送至正电子发射断层扫描 (PET) 和单光子发射计算机断层扫描 (SPECT) 目标组织的高效载体。然而,传统上用于将放射性同位素连接到这些生物分子的随机方法不可避免地会产生定义不明确且异质的探针,并可能削弱免疫球蛋白与分子靶标结合的能力。为应对这一挑战,已经开发出一系列创新的定点和选择性生物缀合策略,这些方法已反复证明可产生更明确和更同质的放射性免疫偶联物,其体内性能优于其随机修饰的前体。在本期《化学生物学新见》评论中,我们将检查该领域的最新进展,包括使用靶向重链聚糖、肽标签和非天然氨基酸的策略标记的核成像剂的开发——在某些情况下已进行临床转化。