下一代生物工艺:组学时代如何影响未来生物治疗发展的行业视角

Chapman Wright, S. Estes
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引用次数: 5

摘要

在过去的十年中,仪器和方法取得了重大进展,使得对代谢物、蛋白质和核酸的分析更加广泛。这反过来又提高了我们对中国仓鼠卵巢(CHO)细胞在生物加工环境中的代谢的复杂性和理解。在上述三个领域中,基因组学在可预见的未来已经成为卓越的技术平台,这主要是由于其吞吐量、全面的覆盖范围和相对简单的工作流程。由于下一代测序(NGS)技术的巨大进步,这种情况得以实现。这些突破以前所未有的速度降低了与全基因组(DNA-Seq)和转录组(RNA-Seq)测序项目相关的成本和时间障碍,为“测序革命”让路。2011年,徐和他的同事们应用NGS技术创建了第一个公开的CHO- k1基因组草图,开创了CHO基因组学的时代。CHO- k1只是生物加工工业利用的少数CHO宿主细胞系之一。事实上,考虑到培养时间的延长和众多实验室对CHO采用的各种适应策略,每个CHO宿主都应被视为一个独特的细胞系,而不管它们是否拥有共同的谱系[3]。因此,在Lewis等人(b[4])和Brinkrolf等人(b[5])的后续出版物中,通过对中国仓鼠基因组进行测序,对CHO-K1草图基因组进行了扩展。获得中国仓鼠参考基因组以促进其他CHO基因组的组装将使整个社区受益。然而,由于测序覆盖范围的差距和不完整的基因注释,基因组的质量受到限制,这项工作远未完成。一个与CHOgenome.org合作的科学家社区目前正在更新和纠正CHO/仓鼠基因组草案,对测序空白和注释特别感兴趣。这项工作对于释放高质量基因组的全部好处至关重要。承认仍有工作要做,问题就变成了:NGS将如何影响未来的生物过程,以及其他“组学”平台的潜在作用是什么?
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Next-generation bioprocess: an industry perspective of how the ‘omics era will affect future biotherapeutic development
The past decade has seen significant instrumentation and methodological advances enabling much broader profiling of metabolites, proteins and nucleic acids. This in turn has been leveraged to enhance our sophistication and understanding of Chinese hamster ovary (CHO) cell metabolism in a bio processing environment. Of the three aforementioned fields, genomics has established itself as the preeminent technology platform for the foreseeable future largely due to a combination of throughput, comprehensive coverage and a relatively simple workflow. This has come to pass as a result of the tremendous advancements in nextgeneration sequencing (NGS) technology. These breakthroughs have lowered the barriers of cost and time associated with whole genome (DNA-Seq) and transcriptome (RNA-Seq) sequencing projects at an unprecedented rate, giving way to the ‘sequencing revolution’ [1]. The era of CHO genomics was ushered in by Xu and co-workers who applied NGS technology to create the first publically available CHO-K1 draft genome in 2011 [2]. CHO-K1 is but one of a handful of CHO host cell lines utilized by the bioprocessing industry. Indeed considering the extended time in culture and variety of adaptation strategies applied by the numerous labs working with CHO, every CHO host should be considered a unique cell line, irrespective of a shared common lineage [3]. Therefore, in subsequent publications by Lewis et al. [4] and Brinkrolf et al. [5] the CHO-K1 draft genome was expanded upon by sequencing the Chinese hamster genome. Having a Chinese hamster reference genome to facilitate the assembly of additional CHO genomes will benefit the community as a whole. However, the work is far from done as the quality of the genome is curtailed by gaps in sequencing coverage and incomplete gene annotations. A community of scientists working with CHOgenome.org is currently in the process of updating and correcting the CHO/hamster draft genomes, with particular interest in the sequencing gaps and annotations. This work will be critical to unlock the full benefits of having a high-quality genome to work with. Acknowledging the work that remains, the question becomes: how will NGS impact future bioprocess and what is the potential role of other ‘omics platforms?
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