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Mass Spectrometric Analysis of Biological Molecules

机译:生物分子的质谱分析

摘要

The investigation of biological molecules through electrospray ionization mass spectrometry has expanded over the past 20 years. With a nanospray source allowing small volumes to be analyzed, perturbation of the sampled system is kept to a minimum. Two studies take advantage of the lack of perturbation to quantitate molecules within biological fluids. The first focuses on the concentration of glucose in tears. A quantitative method is developed to determine the concentration of glucose in human tears. Aqueous solutions of known glucose concentrations and induced tears are used to validate the method. Non-diabetic and diabetic subjects' tears are sampled. After overnight fasting, non-diabetic tear glucose concentration is shown to be 28 ± 14 μM. Tear glucose concentrations from samples taken before and after a meal are compared to the subjects' blood glucose concentrations. The second study that dealt with small biological fluid volumes sought to quantitate neuropeptides within a rat's cerebrospinal fluid. A tapered fused silica capillary is used to obtain cerebrospinal fluid in order to minimize damage to the brain. It was demonstrated that the matrix in the collected biological fluid caused the limit-of-quantitation of the method to be above the neuropeptide concentration within the sample.Protein-RNA complexes are also explored through ESI-MS. The observation of proteins and RNA is demonstrated. Further experiments are performed to determine how many monomers of neuroblastoma apoptosis-related protein bind to RNA during replication. In addition to these biological inquiries, a few silyl containing compounds are examined. Different ionization techniques and collision-induced-dissociation are used to characterize hexamethyldisiloxane, tert-butoxy trimethylsilane, and 2-trimethylsiloxy-propene to determine if they can differentiate volatile organic compounds. Collision-induced-dissocitaion of the silyl ions with argon, acetone-d6, and propanal as the collision gas provided structural identification and possible isomer discrimination. Results show that the ion originating from the loss of a methyl group from hexamethyldisiloxane can provide an avenue to distinguish between acetone and propanal.
机译:在过去的20年中,通过电喷雾电离质谱对生物分子的研究已经扩展。借助纳喷雾源,可以分析小体积样品,将采样系统的扰动降至最低。两项研究利用了缺乏扰动来量化生物流体中分子的优势。第一个重点是眼泪中葡萄糖的浓度。开发了一种定量方法来确定人眼中葡萄糖的浓度。使用已知葡萄糖浓度和诱发泪液的水溶液来验证该方法。非糖尿病和糖尿病受试者的眼泪被采样。过夜禁食后,非糖尿病性眼泪葡萄糖浓度显示为28±14μM。将餐前和餐后采集的样品中的泪糖浓度与受试者的血糖浓度进行比较。第二项涉及较小生物液量的研究试图量化大鼠脑脊髓液中的神经肽。为了使对大脑的损害最小化,使用了锥形熔融石英毛细管来获取脑脊髓液。结果表明,所收集的生物液体中的基质导致该方法的定量限超过了样品中神经肽的浓度.ESI-MS还探索了蛋白质-RNA复合物。证明了蛋白质和RNA的观察。进行进一步的实验以确定在复制过程中神经母细胞瘤凋亡相关蛋白中有多少单体与RNA结合。除了这些生物学查询之外,还检查了一些含甲硅烷基的化合物。使用不同的电离技术和碰撞诱导离解来表征六甲基二硅氧烷,叔丁氧基三甲基硅烷和2-三甲基甲硅烷氧基丙烯,以确定它们是否可以区分挥发性有机化合物。与氩气,丙酮-d6和丙醛作为碰撞气体的碰撞诱导的甲硅烷基离子的解离提供了结构鉴定和可能的异构体识别。结果表明,源自六甲基二硅氧烷的甲基损失的离子可提供区分丙酮和丙醛的途径。

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