1H-Pyrrole-3-propanoicacid, 5-(aminomethyl)-4-(carboxymethyl)-

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CAS: 487-90-1
MF: C10H14N2O4
MW: 226.22916
Synonyms: 1H-Pyrrole-3-propanoicacid, 5-(aminomethyl)-4-(carboxymethyl)-

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He Tian

East China University of Science and Technology
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Chunchang Zhao

East China University of Science & Technology
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Rui Wang

East China University of Science & Technology
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Yi Xiao

Dalian University of Technology
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Co-reporter: Xinfu Zhang, Chao Wang, Zhuo Han, and Yi Xiao
pp: 21669
Publication Date(Web):November 10, 2014
DOI: 10.1021/am506750m
A new boron–dipyrromethene-based lysosome tracker, Lyso-NIR, is facilely synthesized. Besides the intensive near-infrared (NIR) fluorescence and high photostability, Lyso-NIR shows the capability to stably localize in lysosomes, which is independent of the local pH. Lyso-NIR does not have the problematic alkalization effect suffered by the commonly used lysotrackers; thus, it shows ignorable cytotoxicity and slightly affects normal physiological functions of lysosomes. The above advantages of Lyso-NIR make it feasible to track lysosomes’ dynamic changes in a relatively long time during the full cellular processes such as apoptosis, heavy metal stimulation, and endocytosis, as is demonstrated in this work. Moreover, Lyso-NIR’s narrow NIR emission at 740 nm with a full width at half-maximum smaller than 50 nm makes it easy to avoid the crosstalk with the emissions from other common fluorescent probes, which strengthens Lyso-NIR’s competitiveness as a standard lysosome tracker for multicolor bioimaging.Keywords: fluorescence imaging; lysosome; near-infrared; probe

Jack D Henion

Cornell University
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Judith S Sebolt-Leopold

University of Washington
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Frantisek Turecek

University of Washington
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Kevin Burgess

Texas A & M University
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Michael B. Hall

Texas A&M University
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Thomas G. Gray

Case Western Reserve University
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