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使用MUSIC和CC(CO)NH对标准三维核磁共振无法完全解析的两种中等大小蛋白质进行主链归属。

Using MUSIC and CC(CO)NH for backbone assignment of two medium-sized proteins not fully accessible to standard 3D NMR.

作者信息

Brenner Annette K, Frøystein Nils Åge

机构信息

Department of Chemistry, University of Bergen, PO Box 7800, 5020 Bergen, Norway.

出版信息

Molecules. 2014 Jun 26;19(7):8890-903. doi: 10.3390/molecules19078890.

Abstract

The backbone assignment of medium-sized proteins is rarely as straightforward as that of small proteins, and thus often requires creative solutions. Here, we describe the application of a combination of standard 3D heteronuclear methods with CC(CO)NH and a variety of MUltiplicity Selective In-phase Coherence transfer (MUSIC) experiments. Both CC(CO)NH and MUSIC are, in theory, very powerful methods for the backbone assignment of proteins. Due to low sensitivity, their use has usually been linked to small proteins only. However, we found that combining CC(CO)NH and MUSIC experiments simplified the assignment of two challenging medium-sized proteins of 13 and 19.5 kDa, respectively. These methods are to some extent complementary to each other: CC(CO)NH acquired with a long isotropic mixing time can identify amino acids with large aliphatic side chains. Whereas the most sensitive MUSIC experiments identify amino acid types that cannot be detected by CC(CO)NH, comprising the residues with acid and amide groups, and aromatic rings in their side chains. Together these methods provide a means of identifying the majority of peaks in the 2D 15N HSQC spectrum which simplifies the backbone assignment work even for proteins, e.g., small kinases, whose standard spectra resulted in little spectral resolution and low signal intensities.

摘要

中等大小蛋白质的主链归属很少像小蛋白质那样直接,因此通常需要创造性的解决方案。在这里,我们描述了标准3D异核方法与CC(CO)NH以及各种多重性选择性同相相干转移(MUSIC)实验相结合的应用。理论上,CC(CO)NH和MUSIC都是蛋白质主链归属的非常强大的方法。由于灵敏度低,它们的使用通常仅与小蛋白质相关。然而,我们发现将CC(CO)NH和MUSIC实验相结合简化了分别为13 kDa和19.5 kDa的两种具有挑战性的中等大小蛋白质的归属。这些方法在某种程度上相互补充:以长各向同性混合时间获取的CC(CO)NH可以识别具有大脂肪族侧链的氨基酸。而最灵敏的MUSIC实验则识别CC(CO)NH无法检测到的氨基酸类型,包括侧链带有酸基、酰胺基和芳香环的残基。这些方法共同提供了一种识别二维15N HSQC谱中大多数峰的方法,这简化了即使对于标准谱导致谱分辨率低和信号强度弱的蛋白质(例如小激酶)的主链归属工作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5876/6270747/917f36e78f5a/molecules-19-08890-g001.jpg

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