TY - JOUR
T1 - Development of an effective protein-labeling system based on smart fluorogenic probes
AU - Reja, Shahi Imam
AU - Minoshima, Masafumi
AU - Hori, Yuichiro
AU - Kikuchi, Kazuya
N1 - Funding Information:
Acknowledgements This research was partly supported by the Grant-in-Aid for Scientific Research (Grant no. JP16K01933 to M.M., JP18H03935 to K.K. JP17H02210, JP18K19402 to Y. H.), Innovative Areas “Frontier Research on Chemical Communications” (No. JP17H06409) and “Resonance Bio” (No. JP18H04735) of Ministry of Education, Culture, Sports, Science, and Technology (MEXT) of Japan; AMED (Nos. 18he0902005h0004, 17ae0101041h9902, 18fm0208018h0002 to K.K.); JSPS A3 Foresight Program; JSPS CORE-to-CORE Program “Asian Chemical Biology Initiative”; SICORP from JST, and the Asahi Glass Foundation.
Publisher Copyright:
© 2019, Society for Biological Inorganic Chemistry (SBIC).
PY - 2019/6/1
Y1 - 2019/6/1
N2 - Abstract: Proteins are an important component of living systems and play a crucial role in various physiological functions. Fluorescence imaging of proteins is a powerful tool for monitoring protein dynamics. Fluorescent protein (FP)-based labeling methods are frequently used to monitor the movement and interaction of cellular proteins. However, alternative methods have also been developed that allow the use of synthetic fluorescent probes to target a protein of interest (POI). Synthetic fluorescent probes have various advantages over FP-based labeling methods. They are smaller in size than the fluorescent proteins, offer a wide variety of colors and have improved photochemical properties. There are various chemical recognition-based labeling techniques that can be used for labeling a POI with a synthetic probe. In this review, we focus on the development of protein-labeling systems, particularly the SNAP-tag, BL-tag, and PYP-tag systems, and understanding the fluorescence behavior of the fluorescently labeled target protein in these systems. We also discuss the smart fluorogenic probes for these protein-labeling systems and their applications. The fluorogenic protein labeling will be a useful tool to investigate complex biological phenomena in future work on cell biology. Graphical abstract: [Figure not available: see fulltext.].
AB - Abstract: Proteins are an important component of living systems and play a crucial role in various physiological functions. Fluorescence imaging of proteins is a powerful tool for monitoring protein dynamics. Fluorescent protein (FP)-based labeling methods are frequently used to monitor the movement and interaction of cellular proteins. However, alternative methods have also been developed that allow the use of synthetic fluorescent probes to target a protein of interest (POI). Synthetic fluorescent probes have various advantages over FP-based labeling methods. They are smaller in size than the fluorescent proteins, offer a wide variety of colors and have improved photochemical properties. There are various chemical recognition-based labeling techniques that can be used for labeling a POI with a synthetic probe. In this review, we focus on the development of protein-labeling systems, particularly the SNAP-tag, BL-tag, and PYP-tag systems, and understanding the fluorescence behavior of the fluorescently labeled target protein in these systems. We also discuss the smart fluorogenic probes for these protein-labeling systems and their applications. The fluorogenic protein labeling will be a useful tool to investigate complex biological phenomena in future work on cell biology. Graphical abstract: [Figure not available: see fulltext.].
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U2 - 10.1007/s00775-019-01669-y
DO - 10.1007/s00775-019-01669-y
M3 - Review article
C2 - 31152238
AN - SCOPUS:85066458761
SN - 0949-8257
VL - 24
SP - 443
EP - 455
JO - Journal of Biological Inorganic Chemistry
JF - Journal of Biological Inorganic Chemistry
IS - 4
ER -