冷冻电子显微镜用于癌症

Dr Bablee Jyoti, Dr Anand Mohan Jha, Dr Jagadeesh Dhamodharan, Dr Aswinprakash Subramanian
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摘要

冷冻电子显微镜(cryo-EM)的综述论文是必要的,以评估这一革命性的成像技术的最新进展。随着低温电镜技术继续革新结构生物学,全面的综述可以巩固知识,突出技术挑战,并提供对未来发展的见解,促进更好地理解和更广泛地采用这一尖端技术。缺乏关于冷冻电子显微镜用于癌症研究的最新创新方法的综述论文,阻碍了知识的传播和潜在的突破。全面的回顾将弥合差距,阐明冷冻电镜在癌症研究中的成功和挑战,促进合作,并激励进一步的研究,以有效地对抗癌症。”冷冻电子显微镜能够在几乎原子精度的情况下检查生物分子结构,同时捕获多个动态状态,在开发行业首选的冷冻包埋生物大分子在其原生条件下的方法30多年后。技术和设备有了显著改善。研究中采用先进的图像处理方法,促进生物大分子结构的研究和动力学分析;为此,低温电镜是一个强有力的工具。低温电镜必须有效地研究细胞大分子结构,包括使用尖端的图像处理方法进行动态分析。使用电子断层扫描对单个粒子的现代分析甚至更容易适用于该程序。随着单粒子分析和电子层析技术的发展,它的应用越来越广泛。这些技术进一步提高了该方法的适用性。由于其易于使用和能够产生复杂和复杂的数据,可用于更好地理解生物结构,冷冻电镜是目前更受欢迎和可用的研究工具。因此,它成为学术和工业研究的有用工具。蛋白质复合物、分子途径和病毒结构也已使用冷冻电镜进行了研究。由于其适应性,它已成为疾病和药物开发的有用工具。它的低成本和简单的使用也使它成为一个重要的研究工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cryo-Electron Microscopy for Cancer
A review paper on cryo-electron microscopy (cryo-EM) is essential to assess the recent advancements in this revolutionary imaging technique. As cryo-EM continues to revolutionize structural biology, a comprehensive review can consolidate the knowledge, highlight technical challenges, and offer insights into future developments, promoting better understanding and wider adoption of this cutting-edge technology. The absence of a review paper on the recent innovative approach of applying cryo-electron microscopy for cancer research hinders knowledge dissemination and impedes potential breakthroughs. A comprehensive review would bridge the gap, elucidating the successes and challenges of cryo-EM in cancer studies, fostering collaboration, and inspiring further investigations to combat cancer effectively.” Cryo-electron microscopy enables examining biomolecular structures at almost atomic precision while capturing multiple dynamic states more than 30 years after developing the industry's preferred method for cryo-embedding biological macromolecules under their native conditions. Techniques and equipment have significantly improved. Advanced image-processing methods are employed in research to facilitate the study of biological macromolecular structures and analyze their dynamics; for this, cryo-EM is a potent tool. Cryo-EM must effectively investigate the cellular macromolecular structure, including dynamic analysis using cutting-edge image-processing methods. Modern Analysis of individual particles using electron tomography is even more easily applicable to the procedure. With the development of single particle analysis and electron tomography, it is now more broadly applicable. These techniques have increased the method's applicability even further. Due to its ease of use and capacity to produce intricate and sophisticated data that can be used to comprehend biological structures better, cryo-EM is currently a more well-liked and available research tool. As a result, it serves as a useful tool for both academic and industrial research. Protein complexes, molecular pathways, and viral structures have also been studied using cryo-EM. Due to its adaptability, it has become a useful tool for illness and drug development. Its low cost and simplicity of usage have also made it a crucial research tool.
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