深铬移
荧光团
荧光
斯托克斯位移
化学
合理设计
取代基
分子
亮度
光化学
生物传感器
化学物理
纳米技术
生物物理学
材料科学
立体化学
光学
生物
物理
生物化学
有机化学
作者
Xia Wu,Davin Tan,Qinglong Qiao,Wenting Yin,Zhaochao Xu,Xiaogang Liu
摘要
Long-wavelength fluorescent proteins (LWFPs) and LWFP-based sensors are indispensable tools for bioimaging and biosensing applications. However, it remains challenging to develop LWFPs with outstanding brightness and/or sensitivities, largely due to the lack of simple and effective molecular design strategies. Herein, we rationalized the molecular origins of a multi-donor strategy that affords significant bathochromic shifts and large Stokes shifts with minimal structural changes in the resulting protein fluorophores. We analyzed three key factors that affect the spectral properties of these fluorophores, including the (1) substituent position, (2) electron-donating strength, and (3) number of electron-donating groups. We further demonstrated that this simple design strategy is generalizable to various fluorophore families. We expect that this work can provide rational guidelines for developing fluorescent proteins (and small-molecule fluorophores) with long emission wavelengths and large Stokes shifts.
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