Spork Matthias, Sohail Muhammad Imran, Schmid Diethart, Ecker Gerhard F, Freissmuth Michael, Chiba Peter, Stockner Thomas
Institute of Medical Chemistry Center of Pathobiochemistry and Genetics Medical University of Vienna Waehringerstrasse 10 Vienna A-1090 Austria.
Department of Zoology Government College University Lahore Katchery Road Lahore 54000 Pakistan.
Pharmacol Res Perspect. 2017 May 26;5(3):e00325. doi: 10.1002/prp2.325. eCollection 2017 Jun.
Point mutations of ATP-binding cassette (ABC) proteins are a common cause of human diseases. Available crystal structures indicate a similarity in the architecture of several members of this protein family. Their molecular architecture makes these proteins vulnerable to mutation, when critical structural elements are affected. The latter preferentially involve the two transmembrane domain (TMD)/nucleotide-binding domain (NBD) interfaces (transmission interfaces), formation of which requires engagement of coupling helices of intracellular loops with NBDs. Both, formation of the active sites and engagement of the coupling helices, are contingent on correct positioning of ICLs 2 and 4 and thus an important prerequisite for proper folding. Here, we show that active site compounds are capable of rescuing P-glycoprotein (P-gp) mutants ∆Y490 and ∆Y1133 in a concentration-dependent manner. These trafficking deficient mutations are located at the transmission interface in pseudosymmetric position to each other. In addition, the ability of propafenone analogs to correct folding correlates with their ability to inhibit transport of model substrates. This finding indicates that folding correction and transport inhibition by propafenone analogs are brought about by binding to the active sites. Furthermore, this study demonstrates an asymmetry in folding correction with cis-flupentixol, which reflects the asymmetric binding properties of this modulator to P-gp. Our results suggest a mechanistic model for corrector action in a model ABC transporter based on insights into the molecular architecture of these transporters.
ATP结合盒(ABC)蛋白的点突变是人类疾病的常见原因。现有的晶体结构表明该蛋白家族的几个成员在结构上具有相似性。当关键结构元件受到影响时,它们的分子结构使这些蛋白容易发生突变。后者优先涉及两个跨膜结构域(TMD)/核苷酸结合结构域(NBD)界面(传递界面),其形成需要细胞内环的偶联螺旋与NBD结合。活性位点的形成和偶联螺旋的结合都取决于ICL 2和4的正确定位,因此是正确折叠的重要前提。在这里,我们表明活性位点化合物能够以浓度依赖的方式拯救P-糖蛋白(P-gp)突变体∆Y490和∆Y1133。这些运输缺陷突变位于彼此伪对称位置的传递界面处。此外,普罗帕酮类似物纠正折叠的能力与其抑制模型底物运输的能力相关。这一发现表明,普罗帕酮类似物对折叠的纠正和对运输的抑制是通过与活性位点结合实现的。此外,本研究证明了顺式氟哌噻吨在折叠纠正方面的不对称性,这反映了该调节剂与P-gp的不对称结合特性。我们的结果基于对这些转运蛋白分子结构的深入了解,提出了一个模型ABC转运蛋白中校正剂作用的机制模型。