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蚯蚓细胞外血红蛋白在酸性pH下的解离及其在中性pH下的重新缔合。其四级结构的新模型。

The dissociation of the extracellular hemoglobin of Lumbricus terrestris at acid pH and its reassociation at neutral pH. A new model of its quaternary structure.

作者信息

Mainwaring M G, Lugo S D, Fingal R A, Kapp O H, Vinogradov S N

出版信息

J Biol Chem. 1986 Aug 15;261(23):10899-908.

PMID:3733736
Abstract

Lumbricus terrestris HbO2 and HbCO dissociated below pH 5.0; a time-dependent alteration to the met form occurred at pH less than 5 and pH less than 4.5, respectively. The extent of dissociation was unaffected by alkaline earth cations but was decreased by an increase in ionic strength. HbO2 and HbCO exposed to pH 4.0-4.8 were centrifuged to obtain the undissociated pellet (P1) and dissociated supernatant (S1) fractions. S1 was reassociated at pH 7.0 by dialysis against various buffers and then centrifuged to obtain the reassociated pellet (P2) and unreassociated supernatant (S2) fractions. Reassociation was possible only if S1 was dialyzed against water prior to return to neutral pH; otherwise precipitation occurred starting at about pH 5.3. The extent of reassociation varied from about 40 to 80%, was usually higher for HbCO than HbO2, and was unaffected by an increase in ionic strength or by Ca(II). Gel filtration of P2 on Sephacryl S-300 at neutral pH gave one peak IaR, eluting at a slightly greater volume than the native Hb; S1 and S2 gave in addition, three peaks, Ib (200 kDa), II (65 kDa), and III (18 kDa). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis showed that P2 was slightly deficient in subunit M relative to the Hb, that Ib was deficient in subunits D1 and D2 and that II and III consisted of subunits D1 + D2 + T and subunit M, respectively. Scanning transmission electron microscopy of P2 showed that it was smaller than the native hemoglobin: 25 nm in diameter and 16 nm in height, instead of 30 X 20 nm. Comparison of the results of the dissociations of Lumbricus Hb at alkaline pH (Kapp, O. H., Polidori, G., Mainwaring, M., Crewe, A. V., Vinogradov, S. N. (1984) J. Biol. Chem. 259, 628-639) with those obtained in this study suggested that the Hb quaternary structure was not multimeric and that an alternative model had to be considered. In the proposed model it is assumed that subunits D1 and D2 form a scaffolding or "bracelet," decorated with 12 complexes of M and T subunits.

摘要

蚯蚓血红蛋白氧合血红蛋白(HbO₂)和碳氧血红蛋白(HbCO)在pH 5.0以下会发生解离;在pH小于5和pH小于4.5时,分别会出现向高铁血红蛋白形式的时间依赖性转变。解离程度不受碱土金属阳离子影响,但会因离子强度增加而降低。将暴露于pH 4.0 - 4.8的HbO₂和HbCO离心,以获得未解离的沉淀(P1)和解离的上清液(S1)部分。S1在pH 7.0时通过对各种缓冲液进行透析重新缔合,然后离心以获得重新缔合的沉淀(P2)和未重新缔合的上清液(S2)部分。只有当S1在恢复到中性pH之前对水进行透析时,重新缔合才有可能;否则在约pH 5.3时开始出现沉淀。重新缔合的程度在约40%至80%之间变化,通常HbCO的重新缔合程度高于HbO₂,并且不受离子强度增加或Ca(II)的影响。在中性pH下,将P2在Sephacryl S - 300上进行凝胶过滤,得到一个峰IaR,其洗脱体积略大于天然血红蛋白;S1和S2还给出了三个峰,Ib(200 kDa)、II(65 kDa)和III(18 kDa)。十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳表明,相对于血红蛋白,P2中的亚基M略有不足,Ib中缺乏亚基D1和D2,II和III分别由亚基D1 + D2 + T和亚基M组成。对P2的扫描透射电子显微镜观察表明,它比天然血红蛋白小:直径为25 nm,高度为16 nm,而不是30×20 nm。将蚯蚓血红蛋白在碱性pH下的解离结果(卡普,O. H.,波利多里,G.,梅因沃林,M.,克鲁,A. V.,维诺格拉多夫,S. N.(1984年)《生物化学杂志》259,628 - 639)与本研究中获得的结果进行比较,表明血红蛋白的四级结构不是多聚体,必须考虑另一种模型。在提出的模型中,假设亚基D1和D2形成一个支架或“手镯”,上面装饰有12个M和T亚基的复合物。

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