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利用非洲爪蟾卵提取物在体外研究有丝分裂纺锤体的组装和功能。

Investigating mitotic spindle assembly and function in vitro using Xenopus laevis egg extracts.

作者信息

Hannak Eva, Heald Rebecca

机构信息

University of California, Berkeley, 315 Life Sciences Addition, Berkeley, CA 94720-3200, USA.

出版信息

Nat Protoc. 2006;1(5):2305-14. doi: 10.1038/nprot.2006.396.

Abstract

Extracts from Xenopus laevis eggs provide a powerful system for the study of cell division processes in vitro through biochemical reconstitution and manipulation, and microscopic analysis. We provide protocols for the preparation of metaphase-arrested extracts and in vitro assays to examine the following pathways of spindle assembly: 1) Sperm nuclei added to meiotic extracts, supporting the formation of half-spindles and bipolar spindle structures around unreplicated chromosomes; 2) sperm nuclei added to extracts that cycle through interphase and form spindles that are capable of undergoing anaphase and chromosome segregation; and 3) spindle formation around chromatin-coated beads. Finally, we describe methods to inhibit a specific protein by immunodepletion or addition of an inhibitor such as a dominant-negative construct. These techniques can be used to analyze the mitotic function of a given protein. It takes approximately 1.5 h to prepare the extract, 1-3 h for spindle-assembly experiments and an additional 1-3 h if immunodepletion is performed.

摘要

非洲爪蟾卵提取物为体外研究细胞分裂过程提供了一个强大的系统,可通过生化重组与操作以及显微镜分析来实现。我们提供了制备中期阻滞提取物的方案以及体外分析方法,以检测纺锤体组装的以下途径:1)将精子细胞核添加到减数分裂提取物中,支持在未复制染色体周围形成半纺锤体和双极纺锤体结构;2)将精子细胞核添加到经历间期循环并形成能够进行后期和染色体分离的纺锤体的提取物中;3)在染色质包被的珠子周围形成纺锤体。最后,我们描述了通过免疫去除或添加抑制剂(如显性负性构建体)来抑制特定蛋白质的方法。这些技术可用于分析给定蛋白质的有丝分裂功能。制备提取物大约需要1.5小时,纺锤体组装实验需要1 - 3小时,如果进行免疫去除则还需要额外1 - 3小时。

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