Iacobucci Valentina, Di Giuseppe Francesca, Bui Tam T, Vermeer Louic S, Patel Jayneil, Scherman Daniel, Kichler Antoine, Drake Alex F, Mason A James
Institute of Pharmaceutical Science, King's College London, Franklin-Wilkins Building, 150 Stamford Street, London SE1 9NH, UK.
Biochim Biophys Acta. 2012 May;1818(5):1332-41. doi: 10.1016/j.bbamem.2011.12.018. Epub 2011 Dec 29.
Cationic amphipathic histidine rich peptides demonstrate differential nucleic acid binding capabilities at neutral and acidic pH and adopt conformations at acidic pH that enable interaction with endosomal membranes, their subsequent disordering and facilitate entry of cargo to the cell cytosol. To better understand the relative contributions of each stage in the process and consequently the structural requirements of pH responsive peptides for optimal nucleic acid transfer, we used biophysical methods to dissect the series of events that occur during endosomal acidification. Far-UV circular dichroism was used to characterise the solution conformation of a series of peptides, containing either four or six histidine residues, designed to respond at differing pH while a novel application of near-UV circular dichroism was used to determine the binding affinities of the peptides for both DNA and siRNA. The peptide induced disordering of neutral and anionic membranes was investigated using (2)H solid-state NMR. While each of these parameters models key stages in the nucleic acid delivery process and all were affected by increasing the histidine content of the peptide, the effect of a more acidic pH response on peptide self-association was most notable and identified as the most important barrier to further enhancing nucleic acid delivery. Further, the results indicate that Coulombic interactions between the histidine residues modulate protonation and subsequent conformational transitions required for peptide mediated gene transfer activity and are an important factor to consider in future peptide design.
富含组氨酸的阳离子两亲性肽在中性和酸性pH下表现出不同的核酸结合能力,并且在酸性pH下采用能够与内体膜相互作用、随后使其无序化并促进货物进入细胞质溶胶的构象。为了更好地理解该过程中每个阶段的相对贡献,进而了解pH响应肽实现最佳核酸转移的结构要求,我们使用生物物理方法剖析了内体酸化过程中发生的一系列事件。远紫外圆二色性用于表征一系列含有四个或六个组氨酸残基的肽的溶液构象,这些肽被设计为在不同pH下做出响应,同时使用近紫外圆二色性的一种新应用来确定肽对DNA和siRNA的结合亲和力。使用2H固态核磁共振研究了肽诱导的中性和阴离子膜的无序化。虽然这些参数中的每一个都模拟了核酸递送过程中的关键阶段,并且所有这些参数都受到肽中组氨酸含量增加的影响,但更酸性的pH响应对肽自缔合的影响最为显著,并被确定为进一步提高核酸递送的最重要障碍。此外,结果表明组氨酸残基之间的库仑相互作用调节了肽介导的基因转移活性所需的质子化和随后的构象转变,并且是未来肽设计中需要考虑的一个重要因素。