Near-field scanning optical microscopy of single molecules by femtosecond two-photon excitation

被引:30
作者
Lewis, MK [1 ]
Wolanin, P
Gafni, A
Steel, DG
机构
[1] Univ Michigan, Dept Phys, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Biol Chem, Ann Arbor, MI 48109 USA
关键词
D O I
10.1364/OL.23.001111
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
We present a demonstration of near-field scanning optical microscopy of single molecules based on ultrafast two-photon-induced fluorescence. Measurements were performed by use of 100-fs pulses at 800 nm from a Ti:sapphire laser to excite the two-photon transition in Rhodamine B molecules. Although near-field probes are normally metal coated to achieve superresolution, we used uncoated tips to achieve sufficiently high optical powers to generate acceptable fluorescence emission rates. Images of single molecules demonstrate a resolution of similar to 175 nm (< lambda/4) on a topographically smooth surface, which surpasses the apparent lambda/2 resolution limit for uncoated tips operating in the linear response regime. (C) 1998 Optical Society of America.
引用
收藏
页码:1111 / 1113
页数:3
相关论文
共 18 条
[1]   COMBINED SHEAR FORCE AND NEAR-FIELD SCANNING OPTICAL MICROSCOPY [J].
BETZIG, E ;
FINN, PL ;
WEINER, JS .
APPLIED PHYSICS LETTERS, 1992, 60 (20) :2484-2486
[2]   SINGLE MOLECULES OBSERVED BY NEAR-FIELD SCANNING OPTICAL MICROSCOPY [J].
BETZIG, E ;
CHICHESTER, RJ .
SCIENCE, 1993, 262 (5138) :1422-1425
[3]   Single-molecule identification of Coumarin-120 by time-resolved fluorescence detection: Comparison of one- and two-photon excitation in solution [J].
Brand, L ;
Eggeling, C ;
Zander, C ;
Drexhage, KH ;
Seidel, CAM .
JOURNAL OF PHYSICAL CHEMISTRY A, 1997, 101 (24) :4313-4321
[4]   RESOLUTION IN COLLECTION-MODE SCANNING OPTICAL MICROSCOPY [J].
BUCKLAND, EL ;
MOYER, PJ ;
PAESLER, MA .
JOURNAL OF APPLIED PHYSICS, 1993, 73 (03) :1018-1028
[5]   2-PHOTON LASER SCANNING FLUORESCENCE MICROSCOPY [J].
DENK, W ;
STRICKLER, JH ;
WEBB, WW .
SCIENCE, 1990, 248 (4951) :73-76
[6]   NEAR-FIELD FLUORESCENT IMAGING OF SINGLE PROTEINS [J].
DUNN, RC ;
ALLEN, EV ;
JOYCE, SA ;
ANDERSON, GA ;
XIE, XS .
ULTRAMICROSCOPY, 1995, 57 (2-3) :113-117
[7]   Membrane specific mapping and colocalization of malarial and host skeletal proteins in the Plasmodium falciparum infected erythrocyte by dual-color near-field scanning optical microscopy [J].
Enderle, T ;
Ha, T ;
Ogletree, DF ;
Chemla, DS ;
Magowan, C ;
Weiss, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (02) :520-525
[8]   Facts and artifacts in near-field optical microscopy [J].
Hecht, B ;
Bielefeldt, H ;
Inouye, Y ;
Pohl, DW ;
Novotny, L .
JOURNAL OF APPLIED PHYSICS, 1997, 81 (06) :2492-2498
[9]   NANOSCALE COMPLEXITY OF PHOSPHOLIPID MONOLAYERS INVESTIGATED BY NEAR-FIELD SCANNING OPTICAL MICROSCOPY [J].
HWANG, J ;
TAMM, LK ;
BOHM, C ;
RAMALINGAM, TS ;
BETZIG, E ;
EDIDIN, M .
SCIENCE, 1995, 270 (5236) :610-614
[10]   DEVELOPMENT OF A 500-A SPATIAL-RESOLUTION LIGHT-MICROSCOPE .1. LIGHT IS EFFICIENTLY TRANSMITTED THROUGH GAMMA-16 DIAMETER APERTURES [J].
LEWIS, A ;
ISAACSON, M ;
HAROOTUNIAN, A ;
MURAY, A .
ULTRAMICROSCOPY, 1984, 13 (03) :227-231