Yao Yueyu, Wu Jingyun, Hu Yue, Haubold Laura, Uzosike Obinna, Cheng Guangming, Yao Nan, Scholes Gregory D, Hecht Michael H, Spangler Leah C
†Department of Chemistry, ‡Department of Molecular Biology, §Princeton Materials Institute, Princeton University, Princeton, New Jersey 08544, United States.
Department of Chemical and Life Science Engineering, Virginia Commonwealth University, Richmond, Virginia 23284, United States.
ACS Cent Sci. 2025 May 27;11(6):983-993. doi: 10.1021/acscentsci.4c01826. eCollection 2025 Jun 25.
Here, we present the first instance of utilizing proteins to regulate the size of cadmium sulfide (CdS) quantum dots. Four proteins were found to bind to CdS and cap the growth of CdS quantum dots, leading to precise size control, as evidenced by absorbance and fluorescence spectra. Increasing the concentration of CdS does not change the absorbance and emission peaks, thereby indicating that the proteins effectively constrain the size of the quantum dots. Employing different proteins also yielded quantum dots with distinct optical and physical properties, including the appearance of biomediated nanorods when SynI3 was utilized. Moreover, the proteins effectively maintained the stability of the quantum dots for up to 7 days, surpassing the stability of quantum dots capped by the small molecule, l-cysteine. The ability to cap CdS likely stems from their affinities for Cd, yet there does not seem to be a direct correlation between the affinity for Cd and the size of resulting quantum dots.
在此,我们展示了利用蛋白质调控硫化镉(CdS)量子点尺寸的首个实例。发现四种蛋白质可与CdS结合并抑制CdS量子点的生长,从而实现精确的尺寸控制,吸光度和荧光光谱证明了这一点。增加CdS的浓度不会改变吸光度和发射峰,这表明蛋白质有效地限制了量子点的尺寸。使用不同的蛋白质还能产生具有不同光学和物理性质的量子点,例如在使用SynI3时会出现生物介导的纳米棒。此外,这些蛋白质能有效维持量子点长达7天的稳定性,超过了由小分子l-半胱氨酸包覆的量子点的稳定性。包覆CdS的能力可能源于它们对Cd的亲和力,但对Cd的亲和力与所得量子点的尺寸之间似乎没有直接关联。