...
首页> 外文期刊>Analytical chemistry >Two-Dimensional Isoelectric Focusing OFFGEL and Microfluidic Lab-on-Chip Electrophoresis for Assessing Dissolved Proteins in Seawater
【24h】

Two-Dimensional Isoelectric Focusing OFFGEL and Microfluidic Lab-on-Chip Electrophoresis for Assessing Dissolved Proteins in Seawater

机译:二维等电聚焦OFFGEL和微流控芯片电泳法评估海水中的溶解蛋白

获取原文
获取原文并翻译 | 示例
           

摘要

Dissolved proteins were assessed in surface and deep seawater by two-dimensional isoelectric focusing (IEF) OFFGEL-lab-on-chip (LOC) electrophoresis after tangential flow ultrafiltration followed by centrifugal ultrafiltration (preconcentration factor of 3000). Dissolved protein isolation was performed by treating the ultrafiltrated retentate with cold acetone and also with chloroform as precipitating reagents. The best electrophoretic behavior of the isolated proteins was obtained after protein precipitation with chloroform before different rinsing stages for removing methanol and water interferences. Metals bound to proteins in the different OFFGEL fractions were assessed by inductively coupled plasma-optical emission spectrometry and electro-thermal atomic absorption spectrometry, under optimized operating conditions. Experiments regarding stability of the metal-binding proteins [superoxide dismutase (SOD) and alcohol dehydrogenase (ADH) as protein models] showed the integrity of the Zn-binding SOD/ADH under the OFFGEL electrophoretic conditions. However, stability of Cu bound to SOD is not guaranteed. The first electrophoretic dimension (IEF OFFGEL) showed that dissolved proteins in surface seawater exhibit alkaline isoelectric points (pIs of 8.10 and 8.37) and also acid Ips (4.82, 5.13, 5.43, and 5.73), while LOC showed that the isolated proteins exhibit a spread molecular weight range (within 15 - 63 kDa); although, high molecular weights were the most commonly found. Regarding deep seawater, isolated proteins were of acid Ips (from 3.30 to 4.22) and low molecular weight (within the 21-24 kDa range). Elements such as Cd, Cu, Mn, and Ni were mainly associated with dissolved proteins of alkaline pIs in surface seawater, while Zn was mainly associated to proteins of acid pIs. However, only Cu and Mn were found to be bound to dissolved proteins of higher Ips in deep seawater, and the amount of Mn (from 68 to 84 μg L~(-1)) was higher than that found in dissolved proteins in surface seawater (22.4 μg L~(-1)).
机译:切向流超滤,离心超滤(浓缩因子为3000)后,通过二维等电聚焦(IEF)OFFGEL芯片实验室(LOC)电泳,评估了表层和深层海水中的溶解蛋白。溶解的蛋白质分离是通过用冷丙酮和氯仿作为沉淀试剂处理超滤渗余物来进行的。在用氯仿沉淀蛋白质之前,在不同的漂洗阶段去除甲醇和水干扰之前,分离出的蛋白质具有最佳的电泳性能。在最佳操作条件下,通过电感耦合等离子体发射光谱法和电热原子吸收光谱法评估了不同OFFGEL馏分中与蛋白质结合的金属。关于金属结合蛋白[超氧化物歧化酶(SOD)和醇脱氢酶(ADH)作为蛋白模型)的稳定性的实验表明,在OFFGEL电泳条件下,锌结合SOD / ADH的完整性。但是,不能保证与SOD结合的Cu的稳定性。第一电泳尺寸(IEF OFFGEL)显示表面海水中溶解的蛋白质显示碱性等电点(pIs为8.10和8.37),还显示酸性Ips(4.82、5.13、5.43和5.73),而LOC显示分离的蛋白质显示出等电点。分子量分布范围(15-63 kDa以内);尽管,高分子量是最常见的。关于深海水,分离出的蛋白质具有酸性Ips(从3.30至4.22)和低分子量(在21-24 kDa范围内)。镉,铜,锰和镍等元素主要与表层海水中碱性pIs的溶解蛋白有关,而锌主要与酸性pIs的蛋白有关。然而,在深层海水中,只有铜和锰与较高的Ips溶解蛋白结合,而锰的含量(从68至84μgL〜(-1))高于表层海水中的溶解蛋白。 (22.4μgL〜(-1))。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号