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蛋白质与硝酸纤维素相互作用的系统分析,以设计优化的消化方案。

Methodical analysis of protein-nitrocellulose interactions to design a refined digestion protocol.

作者信息

Lui M, Tempst P, Erdjument-Bromage H

机构信息

Molecular Biology Program, Memorial Sloan-Kettering Cancer Center, New York, New York 10021, USA.

出版信息

Anal Biochem. 1996 Oct 15;241(2):156-66. doi: 10.1006/abio.1996.0393.

Abstract

We have analyzed the efficacies of seven different organic solvents, 13 organic bases, and 17 detergents to dissociate electroblotted proteins from nitrocellulose. Most efficient were a 1% piperidine-40% acetonitrile mixture and 1% concentrations of either cetyltrimethylammonium bromide or several polyoxyethylene and zwitterionic detergents at pH > or = 8.5. In general, detergent-promoted elution varied with pH (8.5-->12.0) and temperature (37-->65 degrees C) in a detergent-dependent and protein-dependent manner, making for unpredictable results of any combination. However, Zwittergent 3-16, as the major exception, eluted proteins of different sizes and properties almost equally well at pH 8.5. This preferred effect is not enhanced by addition of organic solvent. In fact, detergent/acetonitrile mixtures were generally less efficient for protein elution. Zwittergent 3-16 (1% in 100 mM NH4HCO3) proved to be the most powerful additive for one-step enzymatic digestion of nitrocellulose-bound proteins, both in terms of highest recoveries (including endoproteinase Lys-C digestions) and general applicability, a major improvement over the use of Tween 80 and hydrogenated Triton X-100. The new digest procedure takes just 2 h to complete and requires 5 ng protease per 1 microliter buffer per 1 mm2 of nitrocellulose; relatively large pieces of membrane (> or = 100 mm2) can be successfully processed. The same detergent is a satisfactory additive for digestion of polyvinylidene difluoridebound proteins as well. Moreover, Zwittergent 3-16 is fully compatible with the usual downstream procedures. It is uv (OD214) transparent and does not interfere with high-performance liquid chromatography in any other way. Apparent incompatibility with direct (i.e., "prechromatography") matrix-assisted laser-desorption ionization time-of-flight mass spectrometry can be either reduced by methanol washing of the dried sample and activation of a low-mass gate or eliminated by a simple microliter cleanup procedure.

摘要

我们分析了七种不同有机溶剂、13种有机碱和17种去污剂从硝酸纤维素上解离电印迹蛋白质的效果。最有效的是1%哌啶 - 40%乙腈混合物以及pH≥8.5时1%浓度的十六烷基三甲基溴化铵或几种聚氧乙烯和两性离子去污剂。一般来说,去污剂促进的洗脱随pH(8.5→12.0)和温度(37→65℃)以依赖去污剂和依赖蛋白质的方式变化,使得任何组合的结果都不可预测。然而,两性离子去污剂Zwittergent 3 - 16是主要例外,在pH 8.5时能几乎同样好地洗脱不同大小和性质的蛋白质。添加有机溶剂并不会增强这种优选效果。实际上,去污剂/乙腈混合物通常对蛋白质洗脱效率较低。事实证明,Zwittergent 3 - 16(100 mM NH4HCO3中1%)无论是在最高回收率(包括内肽酶Lys - C消化)还是一般适用性方面,都是用于一步酶解硝酸纤维素结合蛋白的最有效添加剂,相较于使用吐温80和氢化 Triton X - 100有了重大改进。新的消化程序只需2小时即可完成,每1平方毫米硝酸纤维素每1微升缓冲液需要5纳克蛋白酶;相对较大的膜片(≥100平方毫米)也能成功处理。同样的去污剂对于消化聚偏二氟乙烯结合的蛋白质也是一种令人满意的添加剂。此外,Zwittergent 3 - 16与通常的下游程序完全兼容。它在紫外(OD214)下是透明的,并且不会以任何其他方式干扰高效液相色谱。通过对干燥样品进行甲醇洗涤并激活低质量门控,可以降低与直接(即“预色谱”)基质辅助激光解吸电离飞行时间质谱的明显不兼容性,或者通过简单的微升净化程序消除这种不兼容性。

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