Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, Av. Prof. Egas Moniz, Lisboa 1649-028, Portugal.
Molecules. 2017 Oct 18;22(10):1753. doi: 10.3390/molecules22101753.
The capacity to transport therapeutic molecules across the blood-brain barrier (BBB) represents a breakthrough in the development of tools for the treatment of many central nervous system (CNS)-associated diseases. The BBB, while being protective against infectious agents, hinders the brain uptake of many drugs. Hence, finding safe shuttles able to overcome the BBB is of utmost importance. Herein, we identify a new BBB-translocating peptide with unique properties. For years it was thought that cationic sequences were mandatory for a cell-penetrating peptide (CPP) to achieve cellular internalization. Despite being anionic at physiological pH, PepNeg (sequence (SGTQEEY) is an efficient BBB translocator that is able to carry a large cargo (27 kDa), while maintaining BBB integrity. In addition, PepNeg is able to use two distinct methods of translocation, energy-dependent and -independent, suggesting that direct penetration might occur when low concentrations of peptide are presented to cells. The discovery of this new anionic -BBB peptide allows the development of new delivery systems to the CNS and contributes to the need to rethink the role of electrostatic attraction in BBB-translocation.
跨血脑屏障(BBB)转运治疗分子的能力代表了治疗许多中枢神经系统(CNS)相关疾病的工具开发的突破。BBB 虽然可以防止感染,但却阻碍了许多药物进入大脑。因此,寻找能够克服 BBB 的安全穿梭物至关重要。在这里,我们发现了一种具有独特特性的新 BBB 转运肽。多年来,人们一直认为阳离子序列对于细胞穿透肽(CPP)实现细胞内化是必需的。尽管在生理 pH 值下呈阴离子,但 PepNeg(序列(SGTQEEY)是一种有效的 BBB 转运体,能够携带大的货物(27 kDa),同时保持 BBB 的完整性。此外,PepNeg 能够使用两种不同的转运方法,能量依赖和非依赖,这表明当低浓度的肽被递送到细胞时,可能会发生直接穿透。这种新的阴离子-BBB 肽的发现允许开发新的 CNS 递药系统,并有助于重新思考静电吸引在 BBB 转运中的作用。