Fluorescent biomembrane probe for ratiometric detection of apoptosis

被引:298
作者
Shynkar, Vasyl V.
Klymchenko, Andrey S.
Kunzelmann, Corinne
Duportail, Guy
Muller, Christian D.
Demchenko, Alexander P.
Freyssinet, Jean-Marie
Mely, Yves
机构
[1] Univ Louis Pasteur Strasbourg 1, Fac Pharm, CNRS, Inst Gilbert Laustriat,UMR 7175, F-67401 Illkirch Graffenstaden, France
[2] Kyiv Natl Taras Shevchenko Univ, Dept Phys, UA-01033 Kiev, Ukraine
[3] Univ Strasbourg, INSERM, Unite 143, F-67085 Strasbourg, France
[4] Univ Strasbourg, Inst Hematol & Immunol, F-67085 Strasbourg, France
[5] Palladin Inst Biochem, UA-01030 Kiev, Ukraine
关键词
D O I
10.1021/ja068008h
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Herein, we developed the first ratiometric fluorescent probe for apoptosis detection. This probe incorporates selectively into the outer leaflet of the cell plasma membrane and senses the loss of the plasma membrane asymmetry occurring during the early steps of apoptosis. The high specificity to the plasma membranes was achieved by introduction into the probe of a membrane anchor, composed of a zwitterionic group and a long (dodecyl) hydrophobic tail. The fluorescence reporter of this probe is 4'-(diethylamino)-3-hydroxyflavone, which exhibits excited-state intramolecular proton transfer (ESIPT), resulting in two-band emission highly sensitive to the lipid composition of the biomembranes. Fluorescence spectroscopy, flow cytometry, and microscopy measurements show that the ratio of the two emission bands of the probe changes dramatically in response to apoptosis. This response reflects the changes in the lipid composition of the outer leaflet of the cell plasma membrane because of the exposure of the anionic phospholipids from the inner leaflet at the early steps of apoptosis. Being ratiometric, the response of the new probe can be easily quantified on an absolute scale. This allows monitoring by laser scanning confocal microscopy the degree and spatial distribution of the apoptotic changes at the cell plasma membranes, a feature that can be hardly achieved with the commonly used fluorescently labeled annexin V assay.
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收藏
页码:2187 / 2193
页数:7
相关论文
共 45 条
[1]   Aminophospholipid asymmetry: A matter of life and death [J].
Balasubramanian, K ;
Schroit, AJ .
ANNUAL REVIEW OF PHYSIOLOGY, 2003, 65 :701-734
[2]   Binding of annexin V to membrane products of lipid peroxidation [J].
Balasubramanian, K ;
Bevers, EM ;
Willems, GM ;
Schroit, AJ .
BIOCHEMISTRY, 2001, 40 (30) :8672-8676
[3]   DIFFERENTIATION-DEPENDENT EXPRESSION OF PHOSPHATIDYLSERINE IN MAMMALIAN PLASMA-MEMBRANES - QUANTITATIVE ASSESSMENT OF OUTER-LEAFLET LIPID BY PROTHROMBINASE COMPLEX-FORMATION [J].
CONNOR, J ;
BUCANA, C ;
FIDLER, IJ ;
SCHROIT, AJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3184-3188
[4]   The problem of self-calibration of fluorescence signal in microscale sensor systems [J].
Demchenko, AP .
LAB ON A CHIP, 2005, 5 (11) :1210-1223
[5]   Synthesis and identification of small molecules that potently induce apoptosis in melanoma cells through G1 cell cycle arrest [J].
Dothager, RS ;
Putt, KS ;
Allen, BJ ;
Leslie, BJ ;
Nesterenko, V ;
Hergenrother, PJ .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2005, 127 (24) :8686-8696
[6]   Initial exposed phosphatidylserine levels correlate with cellular response to cytotoxic drugs [J].
Drucker, L ;
Ciobotaro, P ;
Kimchi, O ;
Tohami, T ;
Yarkoni, S ;
Radnay, J ;
Shapira, H ;
Lishner, M .
EUROPEAN JOURNAL OF HAEMATOLOGY, 2003, 70 (02) :98-105
[7]   Neutral fluorescence probe with strong ratiometric response to surface charge of phospholipid membranes [J].
Duportail, G ;
Klymchenko, A ;
Mely, Y ;
Demchenko, A .
FEBS LETTERS, 2001, 508 (02) :196-200
[8]   On the coupling between surface charge and hydration in biomembranes:: Experiments with 3-hydroxyflavone probes [J].
Duportail, G ;
Klymchenko, A ;
Mély, Y ;
Demchenko, AP .
JOURNAL OF FLUORESCENCE, 2002, 12 (02) :181-185
[9]   A receptor for phosphatidylserine-specific clearance of apoptotic cells [J].
Fadok, VA ;
Bratton, DL ;
Rose, DM ;
Pearson, A ;
Ezekewitz, RAB ;
Henson, PM .
NATURE, 2000, 405 (6782) :85-90
[10]  
Gidon-Jeangirard C, 1999, J IMMUNOL, V162, P5712