Bonomini Mario
Department of Medicine, G. d'Annunzio University of Chieti-Pescara, and Unit of Nephrology and Dialysis, SS. Annunziata Hospital, Chieti, Italy.
Proteomics Clin Appl. 2017 Dec;11(11-12). doi: 10.1002/prca.201700112. Epub 2017 Nov 20.
Adsorption of plasma proteins onto the membrane surface during the hemodialysis session represents a key feature of membranes used for chronic dialysis therapy. In this issue of Proteomics-Clinical Applications, Han et al. originally describe how, by using proteomic technologies, the adsorptive properties of two membranes made from the same biomaterial (Polyamix) may have different flux characteristics (low flux and high flux, the former having smaller pore size). A total of 497 differentially expressed proteins were identified in eluates obtained after in vivo hemodialysis: 320 proteins concentrated more in low-flux membrane (predominantly proteins with molecular weight 30-60 kDa) and 177 in high flux (most represented by proteins with molecular weight 10-15 kDa). Use of bioinformatics tools shed light on the involvement of adsorbed proteins in important biological pathways, such as the coagulation cascade and the complement system, again with some differences between the two membranes. The study indicates that flux characteristics of a biomaterial used for hemodialysis membrane strongly influence its adsorptive properties, and that proteomic application may provide information relevant to renal replacement therapy.
血液透析过程中血浆蛋白吸附到膜表面是用于慢性透析治疗的膜的一个关键特征。在本期《蛋白质组学 - 临床应用》中,Han等人首次描述了如何通过蛋白质组学技术,由相同生物材料(聚酰胺混合物)制成的两种膜的吸附特性可能具有不同的通量特征(低通量和高通量,前者孔径较小)。在体内血液透析后获得的洗脱液中总共鉴定出497种差异表达蛋白:320种蛋白在低通量膜中富集更多(主要是分子量为30 - 60 kDa的蛋白),177种在高通量膜中富集更多(最具代表性的是分子量为10 - 15 kDa的蛋白)。使用生物信息学工具揭示了吸附蛋白参与重要生物途径的情况,如凝血级联反应和补体系统,两种膜之间同样存在一些差异。该研究表明,用于血液透析膜的生物材料的通量特征强烈影响其吸附特性,并且蛋白质组学应用可能提供与肾脏替代治疗相关的信息。