Department of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee.
Department of Biochemistry & Cellular and Molecular Biology, University of Tennessee, Knoxville, Tennessee.
Biophys J. 2019 Aug 20;117(4):659-667. doi: 10.1016/j.bpj.2019.07.023. Epub 2019 Jul 22.
The acidity-triggered rational membrane (ATRAM) peptide was designed to target acidic diseases such as cancer. An acidic extracellular medium, such as that found in aggressive tumors, drives the protonation of the glutamic acids in ATRAM, leading to the membrane translocation of its C-terminus and the formation of a transmembrane helix. Compared to healthy cells, cancerous cells often increase exposure of the negatively charged phosphatidylserine (PS) on the outer leaflet of the plasma membrane. Here we use a reconstituted vesicle system to explore how PS influences the interaction of ATRAM with membranes. To explore this, we used two new variants of ATRAM, termed K2-ATRAM and Y-ATRAM, with small modifications at the noninserting N-terminus. We observed that the effect of PS on the membrane insertion pK and lipid partitioning hinged on the sequence of the noninserting end. Our data additionally indicate that the effect of PS on the insertion pK does not merely depend on electrostatics, but it is multifactorial. Here we show how small sequence changes can impact the interaction of a peptide with membranes of mixed lipid composition. These data illustrate how model studies using neutral bilayers, which do not mimic the negative charge found in the plasma membrane of cancer cells, may fail to capture important aspects of the interaction of anticancer peptides with tumor cells. This information can guide the design of therapeutic peptides that target the acidic environments of different diseased tissues.
酸度触发的合理膜(ATRAM)肽被设计用于靶向酸性疾病,如癌症。酸性细胞外环境,如侵袭性肿瘤中发现的环境,会促使 ATRAM 中的谷氨酸质子化,导致其 C 端的膜易位和跨膜螺旋的形成。与健康细胞相比,癌细胞通常会增加细胞膜外叶带负电荷的磷脂酰丝氨酸(PS)的暴露。在这里,我们使用重组囊泡系统来探索 PS 如何影响 ATRAM 与膜的相互作用。为了探索这一点,我们使用了两种新的 ATRAM 变体,称为 K2-ATRAM 和 Y-ATRAM,它们在非插入 N 端有微小的修饰。我们观察到 PS 对膜插入 pK 和脂质分配的影响取决于非插入端的序列。我们的数据还表明,PS 对插入 pK 的影响不仅仅取决于静电作用,而是多因素的。在这里,我们展示了小序列变化如何影响肽与混合脂质组成的膜的相互作用。这些数据说明了使用中性双层进行模型研究,这些模型不能模拟癌细胞质膜中发现的负电荷,可能无法捕获抗癌肽与肿瘤细胞相互作用的重要方面。这些信息可以指导针对不同病变组织酸性环境的治疗性肽的设计。