Octet® “魔法”|一年斩获34篇CNS论文的秘诀
一年一度用到Octet®非标记分子互作分析系统的CNS(Cell, Nature, Science三个顶尖杂志)大巡展时间又到了!Octet®在CNS主刊上发表的文章已经达到了34篇(截至2024年12月27日),总计CNS数量已超过300篇!截止现在,Octet®相关文章和专利总数已经接近20,000篇!


Octet® CNS主刊文章数
每年我们都会统计Octet®在CNS主刊上发表的文章数量,在新冠疫情期间,Octet®参与了大量新冠病毒的研究,因此2020至2022年的CNS文章数量相对较多。2024年的文章中具体使用Octet®分子互作系统进行了哪些研究呢?文末提供这些文章的列表以供参考。
按照研究领域分类

Octet®涉及的应用极为广泛,尤其在机理研究方面,从病原菌侵染到疾病发生及细胞生理相关机制的研究中都发挥了重要作用。分子间相互作用是揭示各种生命活动的基本工具,也自然离不开Octet®。
按照检测分子分类

同时,Octet®非标记分子互作系统作为药物筛选和评估的利器,在药物研发中得到了广泛的应用,包括小分子和抗体药物亲和力的检测、表位鉴定以及浓度测定等。

可见,除了蛋白-蛋白,抗体开发外,Octet®灵敏度完全可以检测化合物和多肽等小分子,甚至大到病毒颗粒,细菌甚至细胞。
按照测试方法分类

多分子实验是指观察多个分析物与固化物之间是否存在竞争或协同结合的现象,往往涉及到3个或3个以上分子,涉及多层结合。这是Octet®相较于ITC等基于液液反应的分子互作技术的优势所在。而双分子实验则专注于两者之间的结合动力学。
在这些文章中
居然有一天就发了三篇Cell文章的最高纪录:

三篇背靠背《Cell》,都离不开Octet®...
也有Octet®数据占所有数据一半以上的文章:

做透Octet®,发Nature!看看教科书级的实验设计
而且其中有8篇是国内的文章:

2024国内Octet® CNS赏析:蛋白、多肽、小分子全覆盖!

分子互作强不强?Octet®说了算!
另外还有同时使用”赛多利斯三剑客”的文章:

赛多利斯三剑客成就一篇NATURE论文!
Octet®分子互作分析系统的优势


非标记Direct Binding是趋势,结果更准确

快速测定亲和力,更加定量化地表征分子互作

无洗涤步骤,可测弱亲和力(解离快)

写入了美国药典,文章多,认可度广

万金油技术,可以用与检测DNA,小分子,蛋白质等各种生物分子

操作简便,耗材及维护成本低
同学们,不要犹豫了,操着你手中的
Octet®互作仪,向着CNS进发吧!

下载文档
《生物层干涉技术应用文集(第三版) 》


- Octet® CNS文章列表(滑动查看) -
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Dual BACH1 regulation by complementary SCF-type E3 ligases.Cell,2024
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Structural basis of TMPRSS2 zymogen activation and recognition by the HKU1 seasonal coronavirus.Cell.2024
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The WDR11 complex is a receptor for acidic-cluster-containing cargo proteins.Cell,2024
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Analysis of the diverse antigenic landscape of the malaria protein RH5 identifies a potent vaccine-induced human public antibody clonotype.Cell,2024
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Multimodal targeting chimeras enable integrated immunotherapy leveraging tumor-immune microenvironment.Cell.2024
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TMPRSS2 and glycan receptors synergistically facilitate coronavirus entry.Cell.2024
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A potent pan-sarbecovirus neutralizing antibody resilient to epitope diversification.Cell.2024
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Preclinical proof of principle for orally delivered Th17 antagonist miniproteins.Cell.2024
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Human coronavirus HKU1 recognition of the TMPRSS2 host receptor.Cell.2024
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Recognition of BACH1 quaternary structure degrons by two F-box proteins under oxidative stress.Cell.2024
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A conserved fertilization complex bridges sperm and egg in vertebrates.Cell.2024
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ITPRIPL1 binds CD3ε to impede T cell activation and enable tumor immune evasion.Cell.2024
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Modulation of FGF pathway signaling and vascular differentiation using designed oligomeric assemblies.Cell.2024
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Vaccine induction of heterologous HIV-1-neutralizing antibody B cell lineages in humans.Cell.2024
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Vaccine induction of CD4-mimicking HIV-1 broadly neutralizing antibody precursors in macaques.Cell,2024
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STK19 positions TFIIH for cell-free transcription-coupled DNA repair.Cell
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IGSF8 is an innate immune checkpoint and cancer immunotherapy target.Cell,2024
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Potent and broad HIV-1 neutralization in fusion peptide-primed SHIV-infected macaques.Cell,2024
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Structure of apolipoprotein B100 bound to the low-density lipoprotein receptor.Nature,2024
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Broadly inhibitory antibodies to severe malaria virulence proteins.Nature,2024
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Design of customized coronavirus receptors.Nature,2024
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Transferrin receptor targeting chimeras for membrane protein degradation.Nature, 2024
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Designed endocytosis-inducing proteins degrade targets and amplify signals.Nature,2024
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Shifts in receptors during submergence of an encephalitic arbovirus.Nature,2024
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NBS1 lactylation is required for efficient DNA repair and chemotherapy resistance.Nature,2024
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Computational design of soluble and functional membrane protein analogues.Nature,2024
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Selective haematological cancer eradication with preserved haematopoiesis.Nature,2024
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Mechanism of single-stranded DNA annealing by RAD52–RPA complex.Nature,2024
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HIV-1 capsids enter the FG phase of nuclear pores like a transport receptor.Nature,2024
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Unsupervised evolution of protein and antibody complexes with a structure-informed language model.Science,2024
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A neutralizing antibody prevents postfusion transition of measles virus fusion protein.Science,2024
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Continuous evolution of compact protein degradation tags regulated by selective molecular glues.Science,2024
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Hepatic glycogenesis antagonizes lipogenesis by blocking S1P via UDPG.Science,2024
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Coupling antigens from multiple subtypes of influenza can broaden antibody and T cell responses.Science,2024