Ag 2 Se quantum dots (QDs) with near-infrared (NIR) fluorescenceh ave been widely utilized in NIR fluorescence imaging in vivo because of their narrow bulk band gap and excellent biocompatibility.H owever,m ost of synthesis methodsf or Ag 2 Se QDs are expensive and the reactants are toxic. Herein, an ew protein-templated biomimetic synthesis approachi sp roposed for the preparation of Ag 2 Se QDs by employing bovines erum albumin (BSA) as at emplate and dispersant. The BSA-templated Ag 2 Se QDs (Ag 2 Se@BSAQ Ds) showed NIR fluorescencew ith high fluorescence quantum yield ( % 21.2 %), excellent biocompatibility and good dispersibility in different media. Moreover, the obtained Ag 2 Se@BSA QDs exhibitedr emarkable photother-mal conversion ( % 27.8 %), which could be used in photothermalt herapy.A samodel application in biomedicine, the Ag 2 Se@BSAQ Ds were used as "gatekeepers" to cap mesoporous silica nanoparticles (MSNs) by meanso fe lectrostatic interaction. By taking the advantages of NIR fluorescencea nd photothermal property of Ag 2 Se@BSA QDs, the obtained MSN-DOX-Ag 2 Se nanoparticles (MDA NPs) were employed as an anoplatformf or combined chemo-photothermal therapy. Compared with free DOX and MDA NPs without NIR laser, the laser-treatedM DA NPs exhibited lower cell viability in vitro, implying that Ag 2 Se@BSA QDs are highly promising photothermal agentsa nd the MDA NPs are potential carriers for chemo-photothermal therapy.