Structured illumination microscopy applications towards liver sinusoidal endothelial cell fenestrations and HIV-1 cell-to-cell transmission

摘要：

In the last decade, the field of far-field super-resolution fluorescence microscopy exploded with multiple schemes for sub-diffraction-limit optical microscopy, culminating in a 2008 Method of the Year designation by Nature Publishing Group. Three general categories now exist: structured illumination microscopy (SIM), localization methods (e.g. PALM, dSTORM, and DH-PSF), and stimulated emission depletion (STED). Linear 3D structured illumination microscopy (3DSIM) provides a factor of two in terms of lateral resolution gain (~110 nm) when compared to confocal microscopy, but in all 3 dimensions -while STED and localization methods have surpassed this, but are mostly limited to 2 dimensions.

作者: G.P.McNerney B.Dale B.Chen T.R.Huser W.Hübner V.C.Cogger D.L.Thompson C.I.(O)ie L.D.DeLeve P.McCourt B.Smedsr(o)d D.G.Le Couteur

作者单位: NSF Center for Biophotonics Science and Technology, University of California Davis, Sacramento, CA 9 Division of Infectious Diseases, Department of Medicine, Immunology Institute, Mount Sinai School of NSF Center for Biophotonics Science and Technology, University of California Davis, Sacramento, CA 9 Centre for Education and Research on Aging and the ANZAC Research Institute, Sydney Medical School, Vascular Biology Research Group, Institute of Medical Biology, University of Troms(o) Norway Division of Gastrointestinal and Liver Diseases and the USC Research Center for Liver Diseases, Univ

会议类型: 国际会议

会议名称: Asia Communications and Photonics Conference and Exhibition(2010亚洲光纤通信与光弹博览会及研讨会 ACP 2010)

会议地点: 上海

会议语种:英文

页码: 373-374

在线出版日期: 2010-12-08（万方平台首次上网日期，不代表论文的发表时间）