Proteomics-Based Transporter Identification by the PICK Method: Involvement of TM7SF3 and LHFPL6 in Proton-Coupled Organic Cation Antiport at the Blood-Brain Barrier.
Toshiki KurosawaYuma TegaYasuo UchidaKei HiguchiHidetsugu TabataTakaaki SumiyoshiYoshiyuki KuboTetsuya TerasakiYoshiharu DeguchiPublished in: Pharmaceutics (2022)
A proton-coupled organic cation (H + /OC) antiporter working at the blood-brain barrier (BBB) in humans and rodents is thought to be a promising candidate for the efficient delivery of cationic drugs to the brain. Therefore, it is important to identify the molecular entity that exhibits this activity. Here, for this purpose, we established the P roteomics-based I dentification of transporter by C rosslinking substrate in K eyhole (PICK) method, which combines photo-affinity labeling with comprehensive proteomics analysis using SWATH-MS. Using preselected criteria, the PICK method generated sixteen candidate proteins. From these, knockdown screening in hCMEC/D3 cells, an in vitro BBB model, identified two proteins, TM7SF3 and LHFPL6, as candidates for the H + /OC antiporter. We synthesized a novel H + /OC antiporter substrate for functional analysis of TM7SF3 and LHFPL6 in hCMEC/D3 cells and HEK293 cells. The results suggested that both TM7SF3 and LHFPL6 are components of the H + /OC antiporter.