Name: 단일 항체 표지를 이용한 막 단백질의 단분자 위치 현미경 (동영상) | JoVE Journal
Uploaded: 2026-03-20T13:10:00.000+00:00
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Description: 학습하세요 단일 항체 표지를 이용한 단분자 위치 현미경으로 T 세포 막 단백질의 나노스케일 항원-항체 상호작용을 시각화하는 방법을. 이 기술은 치료용 항체 연구에 중요한 세포 내 환경에서 직접 관찰을 가능하게 합니다.

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Research reported in this publication was supported by the National Institute of General Medical Sciences of the National Institutes of Health under Award Number R35GM146786 and the College of Liberal Arts and Sciences, University of Illinois Chicago. The content is solely the responsibility of the authors and does not necessarily represent the official views of the National Institutes of Health.

All authors declare that they have no conflicts of interest to disclose.

The organization of plasma membrane proteins plays a vital role in regulating cell function. Conventional fluorescence microscopy techniques are limited by the diffraction limit of light, masking their nanoscale organization. SMLM overcomes this limitation by achieving spatial resolutions of 10-20 nm47, enabling the characterization of their nanoscale assemblies10,48,49. Clustering artifacts in SMLM arise...

The plasma membrane contains a diverse array of proteins that regulate cell mobility, adhesion, sensing, and intercellular communication. Understanding the nanoscale distribution of plasma membrane proteins is important, as protein function is often governed not only by expression levels but also by their spatial organization on the membrane1,2. Notably, many therapeutic antibodies target membrane proteins3,4, making nanoscale investigations essential for understanding how antibody interactions are influenced by the local membrane protein organization. However, precise mapping of membrane protein distribution, single-molecule profiling of their abundance, and real-time monitoring of their dynamic interactions with binding partners remain challenging.
Widely used single-molecule localization microscopy (SMLM) techniques, such as direct stochastic optical reconstruction microscopy (dSTORM)5,6 and DNA-based points accumulation for imaging in nanoscale topography (DNA-PAINT)7, use immunofluorescence (IF) staining for sample labeling. They achieve lateral resolutions of ~ 10 nm and have provided extensive insights into the nanoscale organization of therapeutic membrane targets, including human epidermal growth factor receptor 2 (HER2)8,9, CD2010, T cell receptors11,12,13, programmed death-ligand 114, B cell receptors15,16,17, and CD1917,18. For example, dSTORM studies using the therapeutic monoclonal antibody Trastuzumab to directly detect HER2, a key receptor implicated in breast cancer, have revealed distinct clustering states among HER2-positive patients8, while different therapeutic antibodies have been shown to modulate HER2 clustering9. DNA-PAINT combined with lattice light sheet microscopy has elucidated the oligomeric states and interaction profiles of CD20 in B-cells with therapeutic monoclonal antibodies rituximab, ofatumumab, and obinutuzumab10. Although conventional SMLM provides valuable insights into nanoscale organization, its full potential is limited by traditional IF staining approaches. The quality of the SMLM image is dependent on the IF staining, which in turn is governed by the specificity and affinity of the labeling antibody. Traditional SMLM uses high-affinity antibodies that typically achieve superior IF staining and image quality. However, most therapeutic antibodies interact with membrane receptors of live cells with moderate affinity to minimize off-target side effects19. For instance, bispecific T cell engagers (TCEs) exhibit a lower affinity for CD3, which prevents TCR internalization20,21,22. Such interactions cannot be accurately captured by conventional IF techniques.
We have previously developed a strategy that directly leverages single-molecule antibody-epitope interactions, termed single-antibody labeling (SAL). SAL enables high-density mapping of antibody-epitope interactions while preserving native binding equilibria23. While we have previously reported a protocol for intracellular cytoskeletal and mitochondrial proteins24, SAL on membrane proteins has not been demonstrated. In this protocol, we provide a step-by-step workflow for applying SAL to membrane proteins, demonstrated through the labeling of the tetraspanin CD81, a reported therapeutic target candidate25,26,27,28, in both suspension and adherent cells. Using fluorescently labeled anti-CD81 antibodies to directly probe the spatial distribution of CD81 on U2OS and Jurkat T cells, we demonstrate the application of SAL nanoscale studies of membrane proteins. We termed this strategy as membrane SAL (mSAL). Finally, we describe a clustering-based strategy to reduce the isolated single-molecule detections outside of the cell.
In essence, SAL uses time-lapse single-molecule labeling to capture individual antibody-epitope interactions, and subsequent single-emitter deconvolution yields a super-resolution image based on SMLM. By adjusting antibody concentration and selecting an appropriate non-illuminating interval (NII) between consecutive image frames, SAL matches the antibody on-rate to the single-molecule detection rate, enabling single-molecule localization. SAL requires longer NIIs due to the inherently slow binding kinetics of antibodies, which prolong the image acquisition durations (~3-17 h). SAL is best suited for applications that require precise nanoscale mapping of epitopes and the evaluation of individual antibody-epitope interaction dynamics. Despite its lower throughput, SAL offers unique insight into epitope organization and antibody engagement under near-physiological conditions, making it particularly valuable for characterizing therapeutic antibodies in situ.

<table><tbody><tr><td>anti-CD81 Alexa Fluor 488 Antibody</td><td>Thermo Fisher Scientific</td><td>MA5-44132</td><td>Imaging antibody</td></tr><tr><td>Benchtop centrifuge</td><td>Eppendorf</td><td>5424</td><td></td></tr><tr><td>Bovine serum albumin</td><td>MilliporeSigma</td><td>A7906-100G</td><td></td></tr><tr><td>Chambered cover glass, 8-well</td><td>Cellvis</td><td>C8-1-N</td><td></td></tr><tr><td>DMEM media</td><td>Thermo Fisher Scientific</td><td>11960069</td><td></td></tr><tr><td>Dulbecco&#039;s Phosphate Buffered Saline</td><td>Thermo Fisher Scientific</td><td>14190-144</td><td></td></tr><tr><td>Fetal bovine serum</td><td>MilliporeSigma</td><td>F0926-500ML</td><td></td></tr><tr><td>Glutaraldehyde, 10 %</td><td>Electron Microscopy Sciences</td><td>16120</td><td></td></tr><tr><td>Gold colloids, 100 nm</td><td>Ted Pella</td><td>15711&amp;minus;20</td><td>Fiducial marker</td></tr><tr><td>Immersion oil&amp;nbsp;</td><td>Cargille Laboratories</td><td>16245</td><td></td></tr><tr><td>Inverted microscope&amp;nbsp;equipped with TIRF module</td><td>Nikon Instruments</td><td>Eclipse Ti2-E</td><td>Microscope</td></tr><tr><td>Jurkat E6.1 cell line</td><td>MilliporeSigma</td><td>88042803-1VL</td><td>Suspension cells</td></tr><tr><td>Laser Launch, 6 line</td><td>Oxxius</td><td>L6CC-CS8-1511</td><td>Excitation laser</td></tr><tr><td>Lipofectamine 2000</td><td>Thermo Fisher Scientific</td><td>11668019</td><td>Transfection reagent</td></tr><tr><td>Microcentrifuge tube, 1.5 mL&amp;nbsp;</td><td>VWR</td><td>89000-028</td><td></td></tr><tr><td>Microscopy imaging software</td><td>Nikon Instruments</td><td>NIS-Elements Advanced Research</td><td>Image acqisition software</td></tr><tr><td>Objective, 100x/1.49 CFI APO TIRF&amp;nbsp;</td><td>Nikon Instruments</td><td>MRD01991</td><td>Microscope objective</td></tr><tr><td>Paraformaldehyde, 16 %</td><td>Electron Microscopy Sciences</td><td>15710</td><td></td></tr><tr><td>Penicillin-Streptomycin</td><td>Thermo Fisher Scientific</td><td>15140-122</td><td>Antibiotics</td></tr><tr><td>Poly-L-Lysine solution, 0.01%&amp;nbsp;</td><td>MilliporeSigma</td><td>P4707-50ML</td><td></td></tr><tr><td>Prime 95B sCMOS Camera</td><td>Teledyne Vision Solutions</td><td>01-PRIME-95B-R-M-16-C</td><td>Camera</td></tr><tr><td>RPMI 1640 media</td><td>Thermo Fisher Scientific</td><td>11875-093</td><td>Media for suspension cells</td></tr><tr><td>Sodium azide</td><td>Thermo Fisher Scientific</td><td>19038-1000</td><td></td></tr><tr><td>Sodium borohydride</td><td>MilliporeSigma</td><td>213462-25G</td><td></td></tr><tr><td>T25 culture flasks</td><td>Thermo Fisher Scientific</td><td>169900</td><td></td></tr><tr><td>TetraSpeck microspheres</td><td></td><td></td><td>Fiducial marker</td></tr><tr><td>Tissue culture dish, 100 mm&amp;nbsp;</td><td>Corning</td><td>353003</td><td></td></tr><tr><td>U2OS cell line</td><td>ATCC</td><td>HTB-96</td><td>Adherent cells</td></tr></tbody></table>

single-molecule localization microscopy of membrane proteins using single-antibody labeling

Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling

The plasma membrane defines the cell shape and serves as the interface that governs intercellular communication. Membrane proteins constitute a major class of therapeutic targets; therefore, super-resolving the cell membrane through its constitutive proteins holds great promise in advancing cell biology and antibody therapeutics. In this regard, single-molecule localization microscopy (SMLM) enables nanoscale visualization of protein organizations on biological structures. Despite its importance, applying SMLM to plasma membrane proteins poses unique challenges. In this protocol, we present an effective approach using time-lapse single-antibody labeling (SAL) termed membrane SAL (mSAL). We provide detailed step-by-step instructions, including optimization of the antibody concentration, laser power density, duration of non-illumination intervals, image reconstruction, and density-based cluster analysis, to resolve nanoscale membrane protein distribution and membrane morphology. We use the tetraspanin protein CD81 as the model membrane protein to demonstrate the capability of mSAL on both adherent and suspension mammalian cells. In addition to super-resolving the cell membrane and distributions of membrane proteins, our technique enables the investigation of the pharmacodynamics of therapeutic antibodies interacting with their membrane targets in the native membrane environment.

The mSAL technique described in this protocol enables visualization of single antibody binding events to their corresponding plasma membrane protein targets, producing a super-resolution map of membrane protein distribution. CD81 is used here as a representative example, though the approach is readily adaptable to other membrane proteins.
Immobilizing Jurkat T cells with sufficient spacing between cells ensures membrane epitope accessibility by antibodies and glass surface for fiducials to set...

This protocol describes single-antibody labeling (SAL) to resolve the nanoscale spatial organization of plasma membrane proteins. By leveraging cumulative antibody-epitope interactions at the single-molecule level, membrane SAL (mSAL) maps local epitope distributions while simultaneously capturing antibody binding behavior in the native cellular environment.

The plasma membrane defines the cell shape and serves as the interface that governs intercellular communication. Membrane proteins constitute a major ...

My research focuses on the membrane of T cells and aims to reveal new nanoscale insights relevant to therapeutic targeting. Existing imaging methods do not typically directly visualize nanoscale antibody-epitope interactions in cells. This protocol overcomes that limitation by enabling direct observation within the cellular environment.After mounting the sample on the microscope and depositing gold colloids onto the surface, use bright field illumination to verify that enough colloids have been deposited within the region of interest. Confirm that the ideal density of 5 to 10 gold colloids is present within the region of interest before proceeding. For the optical configuration of the antibody probe fluorophore, open the imaging software and access the optical configuration settings.Select the appropriate dichroic mirror and set the laser excitation wavelength and power density. Adjust the camera integration time and select the emission filter. Then, set the camera pixel binning to achieve a pixel size of 150 to 160 nanometers.Now, create an optical configuration for the photo bleaching step by selecting a photo bleaching mode in the imaging software. Set the laser power to 100%and

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Research

JoVE Journal

Bioengineering

We demonstrate the use of the gene gun to introduce fluorescent dyes, such as DiI, into neurons in brain slices from rodents and non-human primates of different ages. In this particular case, we use adult mice (3-6 months old) and adult cynomologus monkeys (9-15 years old). This technique, originally described by the laboratory of Dr. Lichtman (Gan et al., 2000), is well suited for the study of dendritic branching and dendritic spine morphology and can be combined with traditional...

DiOLISTIC Labeling of Neurons from Rodent and Non-human Primate Brain Slices

Here we describe the instrumentation and methods for detecting single fluorescently-labeled protein molecules interacting with a single DNA molecule suspended between two optically trapped microspheres.

Combining Single-molecule Manipulation and Imaging for the Study of Protein-DNA Interactions

Preparation of protein-functionalized planar glass-supported lipid bilayers, determination of protein mobility within and measurement of protein densities is shown here. A roadmap to building a noise-reduced Total Internal Reflection microscope is outlined, which allows visualizing single bilayer-resident fluorochromes with high spatiotemporal resolution.

Single Molecule Fluorescence Microscopy on Planar Supported Bilayers

PI(4,5)P2 regulates various cellular functions, but its nanoscale organization in the cell plasma membrane is poorly understood. By labeling PI(4,5)P2 with a dual-color fluorescent probe fused to the Pleckstrin Homology domain, we describe a novel approach to study the PI(4,5)P2 spatial distribution in the plasma membrane at the nanometer scale.

Single-molecule Super-resolution Imaging of Phosphatidylinositol 4,5-bisphosphate in the Plasma Membrane with Novel Fluorescent Probes

We demonstrate a method to image multiple molecules within heterogeneous nano-structures at single molecule accuracy using sequential binding and elution of fluorescently labeled antibodies.

Highly Multiplexed, Super-resolution Imaging of T Cells Using madSTORM

Here, we present a protocol for multi-color localization of single membrane proteins in organelles of live cells. To attach fluorophores, self-labeling proteins are used. Proteins, located in different membranes compartments of the same organelle, can be localized with a precision of ~18 nm.

Multi-color Localization Microscopy of Single Membrane Proteins in Organelles of Live Mammalian Cells

We present a protocol for the real-time optical detection of single unlabeled proteins as they are secreted from living cells. This is based on interferometric scattering (iSCAT) microscopy, which can be applied to a variety of different biological systems and configurations.

Label-Free Imaging of Single Proteins Secreted from Living Cells via iSCAT Microscopy

Here, we present a protocol to assess the labeling homogeneity for each protein species in a complex protein sample at the single molecule level.

Proteome-wide Quantification of Labeling Homogeneity at the Single Molecule Level

3D single-molecule localization microscopy is utilized to probe the spatial positions and motion trajectories of fluorescently labeled proteins in living bacterial cells. The experimental and data analysis protocol described herein determines the prevalent diffusive behaviors of cytosolic proteins based on pooled single-molecule trajectories.

Single-Molecule Tracking Microscopy - A Tool for Determining the Diffusive States of Cytosolic Molecules

This protocol describes how to use TIRF microscopy to track individual ion channels and determine their activity in supported lipid membranes, thereby defining the interplay between lateral membrane movement and channel function. It describes how to prepare the membranes, record the data, and analyze the results.

Single-Molecule Imaging of Lateral Mobility and Ion Channel Activity in Lipid Bilayers using Total Internal Reflection Fluorescence (TIRF) Microscopy

This article provides a detailed description of how to create samples for single-protein tracking in solid-supported lipid bilayers. It also explains a straightforward fluorescence microscope with single-molecule sensitivity and a fast frame rate. Finally, we outline the procedure for extracting single-protein trajectories.

Tracking Single Proteins in Lipid Bilayers Using Fluorescence Microscopy

학습하세요 단일 항체 표지를 이용한 단분자 위치 현미경으로 T 세포 막 단백질의 나노스케일 항원-항체 상호작용을 시각화하는 방법을. 이 기술은 치료용 항체 연구에 중요한 세포 내 환경에서 직접 관찰을 가능하게 합니다.

Single-Molecule Localization Microscopy of Membrane Proteins using Single-Antibody Labeling

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