Real-time actin-cytoskeleton depolymerization detection in a single cell using optical tweezers

被引:14
|
作者
De Luca, Anna Chiara
Volpe, Giovanni
Drets, Anna Morales
Geli, Maria Isabel
Pesce, Giuseppe
Rusciano, Giulia
Sasso, Antonio
Petrov, Dmitri
机构
[1] Univ Naples Federico II, Dipartimento Sci Fisiche, I-80126 Naples, Italy
[2] Consorsio Nazl Interuniv Sci Fische Mat Sede, Naples, Italy
[3] Inst Ciencies Foton, E-08860 Barcelona, Spain
[4] Inst Biol Mol Barcelona, CSIC, Barcelona, Spain
[5] Inst Catalana Rec Etudis Avancats, E-08010 Barcelona, Spain
来源
OPTICS EXPRESS | 2007年 / 15卷 / 13期
关键词
MEMBRANE; YEAST; MICRORHEOLOGY; DEFORMABILITY; MOVEMENT; DYNAMICS; TRACKING;
D O I
10.1364/OE.15.007922
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The cytoskeleton provides the backbone structure for the cellular organization, determining, in particular, the cellular mechanical properties. These are important factors in many biological processes, as, for instance, the metastatic process of malignant cells. In this paper, we demonstrate the possibility of monitoring the cytoskeleton structural transformations in optically trapped yeast cells ( Saccharomyces cerevisiae) by tracking the forward scattered light via a quadrant photodiode. We distinguished normal cells from cells treated with latrunculin A, a drug which is known to induce the actin-cytoskeleton depolymerization. Since the proposed technique relies only on the inherent properties of the optical trap, without requiring external markers or biochemical sensitive spectroscopic techniques, it can be readily combined with existing optical tweezers setups. (C) 2007 Optical Society of America
引用
收藏
页码:7922 / 7932
页数:11
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