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ABRF - 98SEQ:高灵敏度肽段测序评估

ABRF-98SEQ: Evaluation of peptide sequencing at high sensitivity.

作者信息

Henzel W J, Admon A, Carr S A, Davis G, De Jongh K, Lane W, Rohde M, Steinke L

机构信息

Department of Protein Biochemistry, Genentech, Inc., South San Francisco, CA 94080, USA.

出版信息

J Biomol Tech. 2000 Jun;11(2):92-9.

Abstract

The ABRF-98SEQ sample was the 11th in a series of amino acid sequencing studies performed by the Protein Sequence Research Group of the Association of Biomolecular Resource Facilities. This study was designed to aid participants' laboratories in determining their abilities to analyze the amino acid sequence of a peptide at high sensitivity using Edman degradation, mass spectrometry (MS), or both. ABRF-98SEQ is a 17-amino acid synthetic peptide (IFDDEIEEVQALYPTER) that resembles a typical tryptic peptide. It was distributed at the 2.8-pmol level. The sample was sent dried in a microfuge tube accompanied by instructions on solubilizing the sample and by a survey form. Including tentative calls, the correct sequence was obtained by 16% of the responding participants, compared with only 6% in the 1997 study when the low-level peptide was a minor component of a mixture. This increase probably reflects the purity of ABRF-98SEQ. A secondary factor in the increase in correct calls may be the larger number of respondents this year reporting that they perform sequence analysis at the 1- to 10-pmol level. Most respondents who obtained the correct sequence used a combination of Edman sequencing and molecular weight determination by MS. Overall, the accuracy and sensitivity of peptide sequencing by Edman degradation continue to improve and are clearly aided by the use of MS for molecular weight determination. Although peptide sequencing by MS is not yet routinely practiced by the participating laboratories, results of this study indicate that MS-derived sequence data, when properly interpreted, are valuable for correcting, completing, or corroborating sequence assignments derived by Edman.

摘要

ABRF - 98SEQ样本是生物分子资源设施协会蛋白质序列研究小组进行的一系列氨基酸测序研究中的第11个。本研究旨在帮助参与实验室确定其使用埃德曼降解法、质谱(MS)或两者结合以高灵敏度分析肽段氨基酸序列的能力。ABRF - 98SEQ是一种由17个氨基酸组成的合成肽(IFDDEIEEVQALYPTER),类似于典型的胰蛋白酶肽段。它以2.8皮摩尔的水平进行分发。样本以干燥状态装在微量离心管中寄出,同时附有样本溶解说明和一份调查问卷。包括初步结果在内,16%的参与应答者获得了正确序列,而在1997年的研究中,当低水平肽是混合物中的次要成分时,只有6%的应答者获得了正确序列。这种增长可能反映了ABRF - 98SEQ的纯度。正确结果增加的另一个因素可能是今年有更多应答者报告他们在1至10皮摩尔水平进行序列分析。大多数获得正确序列的应答者使用了埃德曼测序法和通过质谱测定分子量相结合的方法。总体而言,通过埃德曼降解法进行肽段测序的准确性和灵敏度持续提高,并且使用质谱测定分子量显然有助于提高准确性和灵敏度。虽然参与实验室尚未常规采用质谱法进行肽段测序,但本研究结果表明,质谱衍生的序列数据,若得到正确解读,对于校正、完善或确证通过埃德曼法获得的序列归属很有价值。

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本文引用的文献

1
De novo peptide sequencing via tandem mass spectrometry.通过串联质谱进行从头肽测序。
J Comput Biol. 1999 Fall-Winter;6(3-4):327-42. doi: 10.1089/106652799318300.
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De novo peptide sequencing in an ion trap mass spectrometer with 18O labeling.
Rapid Commun Mass Spectrom. 1998;12(5):209-16. doi: 10.1002/(SICI)1097-0231(19980314)12:5<209::AID-RCM141>3.0.CO;2-S.
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Sequence database searches via de novo peptide sequencing by tandem mass spectrometry.通过串联质谱从头测序进行序列数据库搜索。
Rapid Commun Mass Spectrom. 1997;11(9):1067-75. doi: 10.1002/(SICI)1097-0231(19970615)11:9<1067::AID-RCM953>3.0.CO;2-L.

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