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从海胆卵中分离有丝分裂微管相关蛋白。

Isolation of mitotic microtubule-associated proteins from sea urchin eggs.

作者信息

Bloom G S, Luca F C, Collins C A, Vallee R B

出版信息

Ann N Y Acad Sci. 1986;466:328-39. doi: 10.1111/j.1749-6632.1986.tb38404.x.

DOI:10.1111/j.1749-6632.1986.tb38404.x
PMID:3524371
Abstract

We have used a taxol-based microtubule purification procedure and monoclonal antibodies to isolate and characterize the MAPs of mitotic spindle microtubules in the fertilized sea urchin egg. In so doing, we hope to have identified some of the essential working parts of the mitotic apparatus, namely those proteins that regulate the assembly, disassembly, organization and mechanochemical properties of spindle microtubules. The results of this effort strongly suggest that a rich diversity of polypeptides associate with mitotic spindle microtubules. Whether each of these represents an individual protein species is not currently known. It is possible, for example, that particular spindle MAPs comprise multiple, distinct subunits. This would not be surprising in light of the facts that both MAP-1 and MAP-2 contain lower molecular weight subunits, and that axonemal dyneins are complex assemblies of several polypeptide species. Our future efforts with the sea urchin system will be to determine how the various mitotic spindle MAPs we have identified function individually and in concert, and how those functions contribute to the mechanochemical properties of the spindle.

摘要

我们采用了一种基于紫杉醇的微管纯化方法和单克隆抗体,来分离和鉴定受精海胆卵有丝分裂纺锤体微管的微管相关蛋白(MAPs)。通过这样做,我们希望能够识别出有丝分裂装置的一些关键组成部分,即那些调节纺锤体微管组装、拆卸、组织和机械化学性质的蛋白质。这项工作的结果有力地表明,有多种多肽与有丝分裂纺锤体微管相关联。目前尚不清楚这些多肽是否各自代表一种单独的蛋白质种类。例如,有可能特定的纺锤体微管相关蛋白包含多个不同的亚基。鉴于微管相关蛋白-1(MAP-1)和微管相关蛋白-2(MAP-2)都含有较低分子量的亚基,以及轴丝动力蛋白是几种多肽种类的复杂组装体,这并不奇怪。我们未来在海胆系统上的工作将是确定我们所识别出的各种有丝分裂纺锤体微管相关蛋白如何单独发挥作用以及协同发挥作用,以及这些功能如何对纺锤体的机械化学性质产生影响。

相似文献

1
Isolation of mitotic microtubule-associated proteins from sea urchin eggs.从海胆卵中分离有丝分裂微管相关蛋白。
Ann N Y Acad Sci. 1986;466:328-39. doi: 10.1111/j.1749-6632.1986.tb38404.x.
2
Use of multiple monoclonal antibodies to characterize the major microtubule-associated protein in sea urchin eggs.使用多种单克隆抗体来表征海胆卵中的主要微管相关蛋白。
Cell Motil. 1985;5(6):431-46. doi: 10.1002/cm.970050602.
3
Isolation of sea urchin egg microtubules with taxol and identification of mitotic spindle microtubule-associated proteins with monoclonal antibodies.用紫杉醇分离海胆卵微管并使用单克隆抗体鉴定有丝分裂纺锤体微管相关蛋白。
Proc Natl Acad Sci U S A. 1983 Oct;80(20):6259-63. doi: 10.1073/pnas.80.20.6259.
4
Cytoskeletal architecture of isolated mitotic spindle with special reference to microtubule-associated proteins and cytoplasmic dynein.分离的有丝分裂纺锤体的细胞骨架结构,特别涉及微管相关蛋白和细胞质动力蛋白。
J Cell Biol. 1985 Nov;101(5 Pt 1):1858-70. doi: 10.1083/jcb.101.5.1858.
5
Proteins closely similar to flagellar tektins are detected in cilia but not in cytoplasmic microtubules.在纤毛中检测到与鞭毛轴纤丝蛋白密切相似的蛋白质,但在细胞质微管中未检测到。
Cell Motil. 1985;5(3):239-49. doi: 10.1002/cm.970050306.
6
Identification of kinesin in sea urchin eggs, and evidence for its localization in the mitotic spindle.海胆卵中驱动蛋白的鉴定及其定位于有丝分裂纺锤体的证据。
Nature. 1985;318(6045):483-6. doi: 10.1038/318483a0.
7
Central Spindle Self-Organization and Cytokinesis in Artificially Activated Sea Urchin Eggs.人工激活海胆卵中的中心纺锤体自组织与胞质分裂
Biol Bull. 2016 Apr;230(2):85-95. doi: 10.1086/BBLv230n2p85.
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Mitotic spindle organization by a plus-end-directed microtubule motor.由正端定向微管马达进行的有丝分裂纺锤体组织
Nature. 1992 Oct 8;359(6395):540-3. doi: 10.1038/359540a0.
9
An antiserum to the sea urchin 20 S egg dynein reacts with embryonic ciliary dynein but it does not react with the mitotic apparatus.一种针对海胆20S卵动力蛋白的抗血清与胚胎纤毛动力蛋白发生反应,但不与有丝分裂装置发生反应。
Dev Biol. 1986 Dec;118(2):416-24. doi: 10.1016/0012-1606(86)90012-6.
10
Isolation of microtubules and a dynein-like MgATPase from unfertilized sea urchin eggs.从未受精的海胆卵中分离微管和一种类似动力蛋白的镁ATP酶。
J Biol Chem. 1984 May 25;259(10):6516-25.

引用本文的文献

1
Estramustine binds a MAP-1-like protein to inhibit microtubule assembly in vitro and disrupt microtubule organization in DU 145 cells.雌莫司汀结合一种类微管相关蛋白1以在体外抑制微管组装并破坏DU 145细胞中的微管组织。
J Cell Biol. 1988 Dec;107(6 Pt 2):2647-56. doi: 10.1083/jcb.107.6.2647.