Suppr超能文献

来自水螅虫纲的膝状薮枝螅的钙激活发光蛋白海肾荧光素酶的提取、部分纯化及性质研究

Extraction, partial purification and properties of obelin, the calcium-activated luminescent protein from the hydroid Obelia geniculata.

作者信息

Campbell A K

出版信息

Biochem J. 1974 Nov;143(2):411-8. doi: 10.1042/bj1430411.

Abstract
  1. The Ca(2+)-activated luminescent protein obelin was extracted from the hydroid Obelia geniculata. 2. After the addition of a large excess of calcium (greater than 5mm) a peak in the rate of luminescence occurred within 100ms, followed by an exponential decay (k=2.8s(-1)). The obelin activity (light emitted) was measured by the peak height or by the total number of counts recorded on a scalar in the first 10s after addition of Ca(2+). 3. After an overnight extraction in 40mm-EDTA-200mm-Tris-HCl, pH7.0, 7.2x10(11) counts were obtained from 186g of wet hydroids. 4. The stability of the crude extracts was dependent on pH, being optimal at pH7.0. 5. Obelin could be purified threefold with a yield of 69% by selecting the protein precipitated between 60%- and 100%-saturated (NH(4))(2)SO(4). The precipitate could be stored for at least 6 months as a suspension in 40mm-EDTA+saturated (NH(4))(2)SO(4), pH7.0, frozen at -70 degrees C with a recovery of 95-100%. 6. Luminescence was also stimulated by Sr(2+). However, obelin appeared to have a lower affinity for Sr(2+) than for Ca(2+). Mg(2+) inhibited Ca(2+)-activated luminescence. 7. Obelin could be used to assay as little as 50pmol of Ca(2+) in a final volume of 1ml. 8. At pH7.0 in Ca(2+)-EGTA [ethanedioxybis(ethylamine)tetra-acetate] buffers the rate of obelin luminescence was proportional to the square of the free Ca(2+) concentration in the presence and absence of 1 and 10mm-Mg(2+). Over the range 0.1-10mum-Ca(2+) less than 0.03% of the obelin was consumed/s. 9. In order to use obelin to study free ionized Ca(2+) concentrations similar to those found inside cells in the presence of 10mm-Mg(2+) a minimum of 10(8) counts were required. A total of 10(12) counts can be readily extracted from about 200g of wet hydroids. Thus a sufficient quantity of an aequorin-like calcium-activated luminescent protein should now be available to workers in the United Kingdom in order to carry out physiological experiments.
摘要
  1. 钙激活发光蛋白水母发光蛋白是从水螅纲动物细指海螅中提取的。2. 添加大量过量的钙(大于5毫摩尔)后,发光速率在100毫秒内出现峰值,随后呈指数衰减(k = 2.8秒⁻¹)。水母发光蛋白活性(发出的光)通过峰值高度或添加钙后最初10秒内在标量上记录的总计数来测量。3. 在40毫摩尔 - 乙二胺四乙酸 - 200毫摩尔 - 三羟甲基氨基甲烷盐酸盐(pH7.0)中过夜提取后,从186克湿水螅中获得了7.2×10¹¹计数。4. 粗提物的稳定性取决于pH值,在pH7.0时最佳。5. 通过选择在60%至100%饱和度的硫酸铵中沉淀的蛋白质,水母发光蛋白可以纯化三倍,产率为69%。沉淀物可以作为悬浮液保存在40毫摩尔 - 乙二胺四乙酸 + 饱和硫酸铵(pH7.0)中至少6个月,在 - 70℃冷冻,回收率为95%至100%。6. 锶离子也能刺激发光。然而,水母发光蛋白对锶离子的亲和力似乎比对钙离子的亲和力低。镁离子抑制钙激活的发光。7. 水母发光蛋白可用于在最终体积为1毫升的情况下测定低至50皮摩尔的钙离子。8. 在pH7.0的钙 - 乙二醇双(乙胺)四乙酸缓冲液中,在存在和不存在1和10毫摩尔镁离子的情况下,水母发光蛋白的发光速率与游离钙离子浓度的平方成正比。在0.1至10微摩尔钙离子范围内,每秒消耗的水母发光蛋白不到0.03%。9. 为了使用水母发光蛋白研究在存在10毫摩尔镁离子的情况下与细胞内发现的游离离子化钙离子浓度相似的情况,至少需要10⁸计数。总共10¹²计数可以很容易地从大约200克湿水螅中提取出来。因此,现在英国的研究人员应该有足够数量的类似水母发光蛋白的钙激活发光蛋白来进行生理实验。

相似文献

5
Mn(2+)-activated luminescence of the photoprotein obelin.光蛋白欧贝林的锰(II)激活发光
Arch Biochem Biophys. 1995 Jan 10;316(1):92-9. doi: 10.1006/abbi.1995.1014.
9
Spectral components of bioluminescence of aequorin and obelin.水母发光蛋白和海肾荧光素酶生物发光的光谱成分。
J Photochem Photobiol B. 2008 Aug 21;92(2):117-22. doi: 10.1016/j.jphotobiol.2008.05.006. Epub 2008 May 22.

引用本文的文献

本文引用的文献

7
Depolarization and calcium entry in squid giant axons.枪乌贼巨大轴突中的去极化和钙内流。
J Physiol. 1971 Nov;218(3):709-55. doi: 10.1113/jphysiol.1971.sp009641.
8
Calcium transients in striated muscle cells.
Eur J Cardiol. 1973 Dec;1(2):135-42.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验