IdesignproteinsthatreadDNA

2 nm

My lab builds zinc-finger proteins that find one gene among twenty thousand and switch it on or off. We publish every structure we solve.

02 — Scale

From one base pair to one plate

Cryo-electron tomography
300 kV · 1.2 Å/px
FOV
01 / 05 · 10 nm

Where the protein lands

Our zinc fingers read eighteen letters of DNA. That is enough to find a single address in a genome of three billion.

1 µm
01 — In one paragraph
Structural biologyProtein designGene regulation

02 — Open questions

Three things we still can’t explain

Each question is a project, a grant and at least one argument at lab meeting. We publish what we find, including when the answer is no.

Q1Search kinetics

How does a protein find one gene among twenty thousand?

Zinc fingers scan DNA by sliding and hopping. We time each step with single-molecule imaging and model the search.

Q2Gene activation

Can we switch a gene on without cutting DNA?

Our activators recruit the cell’s own machinery. No breaks, no scars, and the edit fades when the protein does.

Q3Tissue context

Why do identical edits behave differently in tissue?

The same switch works in one cell and stalls in its neighbour. We map chromatin state across whole organoids to find out why.

05 — Selected work

Six projects, one question each

Drag or scroll sideways. Each slide is a project page with the methods, the people and the data behind it.

All research
OR-212026 · Ongoing
Imaging organoids in three colours

Imaging organoids in three colours

A light-sheet pipeline that images whole organoids every twenty minutes without bleaching them.

Imaging1,280
KS-042026 · Ongoing
Proteins with a built-in clock

Proteins with a built-in clock

Designs that the cell clears on a schedule, so an experiment can have a defined start and end.

Protein design5 days
ZF-172025 · Published
Reading eighteen letters of DNA

Reading eighteen letters of DNA

A designed protein that recognises one eighteen-letter stretch of DNA, and the measurements that show how tightly it holds.

Protein design4 nM
HT-122025 · Method
A thousand designs a week on one bench

A thousand designs a week on one bench

An open, low-cost screening pipeline that lets one person characterise a thousand protein designs in a week.

Automation1,152
EM-092024 · Published
A cryo-EM atlas of proteins on nucleosomes

A cryo-EM atlas of proteins on nucleosomes

Fourteen structures showing how designed proteins meet packaged DNA, and why the angle of approach matters.

Structural biology2.9 Å
SM-032023 · Published
Timing a protein’s search along DNA

Timing a protein’s search along DNA

Tracking single molecules as they slide and hop along DNA, and a two-number model that predicts how long the search takes.

Biophysics38 s
05 — Figure 1

What the data actually look like

Hover the plot to read values. Every panel is redrawn from the numbers in our papers, not a screenshot.

Hover to read values
07 — By the numbers

Ten years, counted honestly

0citations since 2016
0papers, 11 as senior author
0structures in the PDB
€0.0Min active grants
Citations per year, 2015–2026
08 — Publications

What we have published lately

Eight recent papers. Every one links to the journal and, where we have it, the raw data.

All publications
2026

Low-dose light-sheet imaging of three-dimensional cultures

Ferreira A., Weber J., Maraval I.

Journal of Cell Science
Preprint
9cited
2025

Designed zinc-finger proteins that read an eighteen-base site

Okafor R., Lindqvist S., Maraval I.

Nature Structural & Molecular Biology
Article
142cited
2025

Open hardware for high-throughput protein screens

Weber J., Nair P., Maraval I.

Nucleic Acids Research
Methods
61cited
2024

A structural atlas of designed proteins bound to nucleosomes

Okafor R., Brandt T., Maraval I.

Cell
Article
318cited
09 — Methods

How we see things this small

Cryo-EM density · 2.9 ÅDesign round 14 · 1,152 candidatesConfocal · 488 / 405 nmLight-sheet · 10× waterPlate reader · Ex 485 / Em 528
Cryo-EM density · 2.9 Å01 / 05
09 — Methods

How we see things this small

Cryo-EM density · 2.9 ÅDesign round 14 · 1,152 candidatesConfocal · 488 / 405 nmLight-sheet · 10× waterPlate reader · Ex 485 / Em 528
Cryo-EM density · 2.9 Å01 / 05
10 — The lab

Eleven people, one microscope queue

A group of physicists, chemists and biologists who all had to learn each other’s vocabulary.

Meet the lab
Ilse Maraval, Group leader
Group leader · Since 2019

Ilse Maraval

Structural biology and protein design. Trained as a physicist.

Rana Okafor, Postdoc
Postdoc · Since 2022

Rana Okafor

Cryo-EM of designed proteins on packaged DNA.

Sten Lindqvist, Postdoc
Postdoc · Since 2021

Sten Lindqvist

Computational design and molecular dynamics.

Mei Tanaka, PhD student
PhD student · Since 2023

Mei Tanaka

Single-molecule tracking in living cells.

10 — Path

Read from 5′ to 3′

The short version of a long CV. The full PDF has every grant, student and committee.

2024

Associate Professor, Kessrow Institute

Group leader since 2019, tenured in 2024.

Structural biology · 11 people
2019

Group leader, Kessrow Institute

Started the lab with one microscope and two students.

ERC Starting Grant
2015

Postdoc, Laboratory of Molecular Structure

First zinc-finger activator solved on DNA by cryo-EM.

EMBO Fellowship
2014

PhD in Biochemistry

How transcription factors find their sites, measured one molecule at a time.

Thesis prize
2009

MSc Physics

Moved from optics to biology by way of a microscope I built.

With distinction
12 — Talks

Where to hear this in person

Three talks coming up and a list of the last few. Slides on request, always.

All talks
12 Mar2026

What a failed screen is worth

Gordon Research Conference
Ventura
Upcoming
12 Mar2026

Reading DNA with designed proteins

EMBO Workshop on Chromatin
Heidelberg
Upcoming
12 Mar2026

Seeing molecules: an evening for schools

Kessrow Institute Open Night
Leiden
Upcoming
12 Mar2026

Fourteen structures and what they changed

Annual Structural Biology Meeting
Basel
Plenary
13 — Journal

Notes from the bench

Short posts about method, failure and how we run the lab.

All posts
Lab notesSep 4, 20266 min

What a failed screen taught us about packaged DNA

Nine hundred designs did nothing. The pattern in which ones did nothing turned out to be the most useful result of the year.

Lab lifeJul 22, 20265 min

How we choose what to work on

Three questions we ask before a project starts, and the one we ask six months in.

Lab lifeMay 30, 20264 min

A microscope you can book on day one

Why every new person gets instrument time in their first week, before they know what they are doing.

Questions, collaborations and PhD applications all welcome.

ilse@maraval-lab.org

Visit

  • Kessrow Institute, Room 4.12
  • 52.1601° N, 4.4970° E
  • Local time
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