1IntroductionIn the past years,p hospholipid bilayer vesicles,n amely liposomes,h ave been useda sm odel cell membranes to investigate the manner and mechanism of the proteinmembrane interactions [1][2][3][4][5].A st he research on proteinmembrane interaction is of greati mportance in the fields of biology,m edical care,a griculture and so on, the developmento fn ovel technologies for simple,f ast and lowcost characterization of protein-membranei nteraction withoutl abeling is significantly required. Recently,m icrocantilever sensors have attracted increasing attention for biomedical applications [6][7][8][9][10][11][12][13].H owever, there are few literatures reporting label-free evaluation of proteinmembrane interaction using micro-cantilever. As the principle of micro-cantilever biosensor is that targetb iomolecules are detectedb ym easuring the deflection of cantilever caused by the interaction betweent he sensing biomolecules immobilizedo nt he cantilever and target biomolecules [6],w ec onsidert hat it is as uitable device for characterization of protein-membrane interaction. Therefore,w ea ttempt to establish ae ffective evaluation system for characterization of variousp rotein-membrane interactions based on amicro-cantilever biosensor.At present, there seems to be some obstaclest or ealize full potential of cantilever-based biosensor. Firstly,i nstead of complex and expensive optical method for measuring the deflection of cantilever [6][7][8][9],e lectricalm ethod has been developed by fabricating the cantilever with the silicon (or silicon compound) piezoresistance,w here the deflection can be translated into electricals ignal for simple and easy measurements [10][11][12][13].H owever,i th as been found that the signal of p + -Si piezoresistancei sn ot stable during measurement due to its high temperature coefficient of resistance (TCR) [14].T herefore,f urther improvementi nt he electrical method for measuring the deflection of cantilever is necessary.S econdly,t here exist two waysi np rinciple for detectioni nl iquid;o ne is as taticm easurement by immersing the cantilever in an opened large liquidc ell (0.8-10 mL) filled with target protein solution [8,11],a nd the other is ad ynamic measurement in the fluid solution which flowst hroughacell and is controlled by ap ump [6,7,13].H owever,t he both methodsr equire large amounts of reagents.I np articular, the fluid liquid mentioned in the dynamic methodm ay have more influence on the stability and accuracyo fm easurement thant he static one if the liquid flow is not precisely controlled. Furthermore,t he influence of solution evaporation on the stability of liquid condition is another serious obstacle. In order to further improve the performance of microcantilever biosensor, some modifications 1) insertion of NiCr thin film strain gauge in the cantilever instead of silicon piezoresistance and 2) fabrication of an ew dropletsealing structure on the cantilever sensor, have been attempted [15].T ob es pecific, for 1), as it has been confirmed that TCR of ...