二肽基肽酶IV及其抑制剂共结构的综合分析

IF 2.222 Q3 Biochemistry, Genetics and Molecular Biology BMC Structural Biology Pub Date : 2016-08-05 DOI:10.1186/s12900-016-0062-8
Hiroyuki Nojima, Kazuhiko Kanou, Genki Terashi, Mayuko Takeda-Shitaka, Gaku Inoue, Koichiro Atsuda, Chihiro Itoh, Chie Iguchi, Hajime Matsubara
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引用次数: 18

摘要

我们综合分析了二肽基肽酶IV (DPP-4)及其抑制剂的x射线共晶结构,以明确DPP-4是否会根据所使用的抑制剂改变其总体或部分结构,以及DPP-4是否具有抑制剂结合的共同规律。尽管与各种形状的抑制剂结合,但除了少数侧链外,抑制剂结合区的所有主链和侧链都被最小程度地改变。该区域的一些残基(Arg125、Glu205、Glu206、Tyr662和Asn710)具有结合模式,可以将抑制剂的特定原子固定在DPP-4中的特定空间位置。我们发现了92个DPP-4结构共有的两个特定的水分子。这两个水分子与许多抑制剂接近,似乎起着两个作用:通过水分子的网络维持Glu205和Glu206侧链的取向,并将抑制剂适当地安排在S2亚位上。我们基于高质量资源的研究可能为发现具有商业价值的新型DPP-4抑制剂提供必要的最小共识。
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Comprehensive analysis of the Co-structures of dipeptidyl peptidase IV and its inhibitor

We comprehensively analyzed X-ray cocrystal structures of dipeptidyl peptidase IV (DPP-4) and its inhibitor to clarify whether DPP-4 alters its general or partial structure according to the inhibitor used and whether DPP-4 has a common rule for inhibitor binding.

All the main and side chains in the inhibitor binding area were minimally altered, except for a few side chains, despite binding to inhibitors of various shapes. Some residues (Arg125, Glu205, Glu206, Tyr662 and Asn710) in the area had binding modes to fix a specific atom of inhibitor to a particular spatial position in DPP-4. We found two specific water molecules that were common to 92 DPP-4 structures. The two water molecules were close to many inhibitors, and seemed to play two roles: maintaining the orientation of the Glu205 and Glu206 side chains through a network via the water molecules, and arranging the inhibitor appropriately at the S2 subsite.

Our study based on high-quality resources may provide a necessary minimum consensus to help in the discovery of a novel DPP-4 inhibitor that is commercially useful.

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来源期刊
BMC Structural Biology
BMC Structural Biology 生物-生物物理
CiteScore
3.60
自引率
0.00%
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0
期刊介绍: BMC Structural Biology is an open access, peer-reviewed journal that considers articles on investigations into the structure of biological macromolecules, including solving structures, structural and functional analyses, and computational modeling.
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