Cryosectioning-enhanced super-resolution microscopy for single-protein imaging across cells and tissues

J Johannes Stein (Wyss Institute of Biologically Inspired Engineering) M Maria Ericsson (Blavatnik Institute, Harvard Medical School) M Michel Nofal (Wyss Institute of Biologically Inspired Engineering) L Lorenzo Magni (Wyss Institute of Biologically Inspired Engineering) S Sarah Aufmkolk (Department of Genetics, Harvard Medical School) R Ryan B. McMillan (Wyss Institute of Biologically Inspired Engineering) L Laura Breimann (Department of Genetics, Harvard Medical School) C Conor P. Herlihy (Department of Genetics, Harvard Medical School) S S. Dean Lee (Department of Genetics, Harvard Medical School) A Andréa Willemin (Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Epigenetic Regulation and Chromatin Architecture Group) J Jens Wohlmann (Department of Biosciences, University of Oslo) L Laura Arguedas-Jimenez (Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Epigenetic Regulation and Chromatin Architecture Group) P Peng Yin (Wyss Institute of Biologically Inspired Engineering) A Ana Pombo G George M. Church C Chao-ting Wu (Department of Genetics, Harvard Medical School)

Abstract

DNA-points accumulation for imaging in nanoscale topography (DNA-PAINT) enables nanoscale imaging with virtually unlimited multiplexing and molecular counting. Here, we address challenges, such as variable imaging performance and target accessibility, that can limit its broader applicability. Specifically, we enhance its capacity for robust single-protein imaging and molecular counting by optimizing the integration of total internal reflection fluorescence microscopy with physical sectioning, in particular, Tokuyasu cryosectioning. Our method, tomographic and kinetically enhanced DNA-PAINT (tkPAINT), achieves 3 nm localization precision across diverse samples, enhanced imager binding, and improved cellular integrity. tkPAINT can facilitate molecular counting with DNA-PAINT inside the nucleus, as demonstrated through its quantification of the in situ abundance of RNA Polymerase II in both HeLa cells as well as mouse tissues. Anticipating that tkPAINT could become a versatile tool for the exploration of biomolecular organization and interactions across cells and tissues, we also demonstrate its capacity to support multiplexing, multimodal targeting of proteins and nucleic acids, and three-dimensional (3D) imaging.

Article Details

Volume / Issue Vol. 122, Issue 32
Published August 12, 2025
ISSN 0027-8424
Publisher National Academy of Sciences

Authors (16)

J

Johannes Stein

Wyss Institute of Biologically Inspired Engineering

M

Maria Ericsson

Blavatnik Institute, Harvard Medical School

M

Michel Nofal

Wyss Institute of Biologically Inspired Engineering

L

Lorenzo Magni

Wyss Institute of Biologically Inspired Engineering

S

Sarah Aufmkolk

Department of Genetics, Harvard Medical School

R

Ryan B. McMillan

Wyss Institute of Biologically Inspired Engineering

L

Laura Breimann

Department of Genetics, Harvard Medical School

C

Conor P. Herlihy

Department of Genetics, Harvard Medical School

S

S. Dean Lee

Department of Genetics, Harvard Medical School

A

Andréa Willemin

Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Epigenetic Regulation and Chromatin Architecture Group

J

Jens Wohlmann

Department of Biosciences, University of Oslo

L

Laura Arguedas-Jimenez

Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association, Berlin Institute for Medical Systems Biology, Epigenetic Regulation and Chromatin Architecture Group

P

Peng Yin

Wyss Institute of Biologically Inspired Engineering

A

Ana Pombo

G

George M. Church

C

Chao-ting Wu

Department of Genetics, Harvard Medical School