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通过免疫吸附鉴定的海胆驱动蛋白轻链

Light chains of sea urchin kinesin identified by immunoadsorption.

作者信息

Johnson C S, Buster D, Scholey J M

机构信息

Department of Zoology, University of California, Davis 95616.

出版信息

Cell Motil Cytoskeleton. 1990;16(3):204-13. doi: 10.1002/cm.970160307.

DOI:10.1002/cm.970160307
PMID:2142020
Abstract

Previous studies with monoclonal antibodies indicate that sea urchin kinesin contains two heavy chains arranged in parallel such that their N-terminal ends fold into globular mechanochemical heads attached to a thin stalk ending in a bipartite tail [Scholey et al., 1989]. In the present, complementary study, we have used the monoclonal antikinesin, SUK4, to probe the quaternary structure of sea urchin (Strongylocentrotus purpuratus) kinesin. Kinesin prepared from sea urchin cytosol sedimented at 9.6 S on sucrose density gradients and consisted of 130-kd heavy chains plus an 84-kd/78 kd doublet (1 mol heavy chain: 1 mol doublet determined by gel densitometry). Low levels of 110-kd and 90-kd polypeptides were sometimes present as well. The 84-kd/78 kd polypeptides are thought to be light chains because they were precipitated from the kinesin preparation at a stoichiometry of one mol doublet per 1 mol heavy chain using SUK4-Sepharose immunoaffinity resins. The 110-kd and 90-kd peptides, by contrast, were removed using this immunoadsorption method. SUK4-Sepharose immunoaffinity chromatography was also used to purify the 130-kd heavy chain and 84-kd/78-kd doublet (1 mol heavy chain: 1 mol doublet) directly from sea urchin egg cytosolic extracts, and from a MAP (microtubule-associated protein) fraction eluted by ATP from microtubules prepared in the presence of AMPPNP but not from microtubules prepared in ATP. The finding that sea urchin kinesin contains equimolar quantities of heavy and light chains, together with the aforementioned data on kinesin morphology, suggests that native sea urchin kinesin is a tetramer assembled from two light chains and two heavy chains.

摘要

先前使用单克隆抗体进行的研究表明,海胆驱动蛋白包含两条平行排列的重链,其N末端折叠成球状的机械化学头部,连接到一个细柄上,细柄末端是一个二分尾 [肖利等人,1989年]。在本补充研究中,我们使用单克隆抗驱动蛋白SUK4来探究海胆(紫球海胆)驱动蛋白的四级结构。从海胆细胞溶质中制备的驱动蛋白在蔗糖密度梯度上以9.6 S沉降,由130-kd重链加上一个84-kd/78 kd双峰组成(通过凝胶光密度法测定,重链与双峰的摩尔比为1:1)。有时也会出现少量的110-kd和90-kd多肽。84-kd/78 kd多肽被认为是轻链,因为使用SUK4-琼脂糖免疫亲和树脂从驱动蛋白制剂中沉淀时,其化学计量比为每1摩尔重链对应1摩尔双峰。相比之下,110-kd和90-kd肽段可通过这种免疫吸附方法去除。SUK4-琼脂糖免疫亲和色谱法还用于直接从海胆卵细胞溶质提取物以及从在AMPPNP存在下制备的微管中由ATP洗脱的微管相关蛋白(MAP)组分中纯化130-kd重链和84-kd/78-kd双峰(1摩尔重链:1摩尔双峰),但不能从在ATP中制备的微管中纯化。海胆驱动蛋白含有等摩尔量的重链和轻链这一发现,连同上述关于驱动蛋白形态的数据,表明天然海胆驱动蛋白是由两条轻链和两条重链组装而成的四聚体。

相似文献

1
Light chains of sea urchin kinesin identified by immunoadsorption.通过免疫吸附鉴定的海胆驱动蛋白轻链
Cell Motil Cytoskeleton. 1990;16(3):204-13. doi: 10.1002/cm.970160307.
2
Inhibition of kinesin-driven microtubule motility by monoclonal antibodies to kinesin heavy chains.抗驱动蛋白重链单克隆抗体对驱动蛋白驱动的微管运动的抑制作用。
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The carboxyl-terminal domain of kinesin heavy chain is important for membrane binding.驱动蛋白重链的羧基末端结构域对于膜结合很重要。
J Biol Chem. 1994 Jan 14;269(2):1477-85.
4
Identification of globular mechanochemical heads of kinesin.
Nature. 1989 Mar 23;338(6213):355-7. doi: 10.1038/338355a0.
5
Sequences of sea urchin kinesin light chain isoforms.海胆驱动蛋白轻链亚型的序列。
J Mol Biol. 1993 May 5;231(1):155-8. doi: 10.1006/jmbi.1993.1267.
6
Purification of kinesin-related protein complexes from eggs and embryos.从卵子和胚胎中纯化驱动蛋白相关蛋白复合物。
Biophys J. 1995 Apr;68(4 Suppl):158S-160S; discussion 160S-162S.
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A microtubule-activated ATPase from sea urchin eggs, distinct from cytoplasmic dynein and kinesin.一种来自海胆卵的微管激活ATP酶,与细胞质动力蛋白和驱动蛋白不同。
Proc Natl Acad Sci U S A. 1986 Jul;83(13):4799-803. doi: 10.1073/pnas.83.13.4799.
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Roles of kinesin and kinesin-like proteins in sea urchin embryonic cell division: evaluation using antibody microinjection.驱动蛋白和类驱动蛋白在海胆胚胎细胞分裂中的作用:通过抗体显微注射进行评估
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Characterization of the microtubule movement produced by sea urchin egg kinesin.海胆卵驱动蛋白产生的微管运动的特征描述。
J Biol Chem. 1987 Feb 25;262(6):2794-802.
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Novel heterotrimeric kinesin-related protein purified from sea urchin eggs.从海胆卵中纯化出的新型异源三聚体驱动蛋白相关蛋白。
Nature. 1993 Nov 18;366(6452):268-70. doi: 10.1038/366268a0.

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