Dr Peter Adams
- Position: Associate Professor
- Areas of expertise: biophysics; photosynthesis; light-harvesting proteins; lipid membranes; atomic force microscopy (AFM); fluorescence spectroscopy; fluorescence lifetime imaging micrscopy (FLIM); nanomaterials.
- Email: P.G.Adams@leeds.ac.uk
- Phone: +44(0)113 343 9718
- Location: 1.12d Sir William Henry Bragg Building
- Website: MNP group page | Adams group @Astbury Centre | Twitter | Googlescholar | ORCID
I am an Associate Professor (a lecturer) in the School of Physics and Astronomy and a part of the Molecular and Nanoscale Physics research group (2015-current). This followed a Postdoctoral Research Scholar position at Los Alamos National Laboratory, USA (2012-2014), and PhD (2007-2011) and BSc (2004-2007) at University of Sheffield, UK.
PhD opportunities with my group available for applications now! These are for a start date of 1st Oct 2023, with various funding opportunities. You are welcome to contact me directly if you are interested:
Fluorescence Lifetime Imaging Microscopy and lipid membrane electrophoresis project: "Revealing the mechanism of photoprotection in light-harvesting proteins using novel nanotechnology and advanced time-resolved fluorescence microscopy". Additional supervision will be provided by lipid membrane expert Prof. Steve Evans.
Electron Microscopy and Fluorescence Spectroscopy project: "Assessing the role of plant membrane proteins in harnessing solar energy with video-speed electron microscopy and fluorescence microscopy". Additional supervision will be provided by EM expert Dr Ste Muench.
Computer simulations and Fluorescence Microscopy project: "Filming photosynthesis: using molecular dynamics simulations and fluorescence to assess the dynamics of the Light Harvesting Complex II protein". Main supervisor will be MD simulation expert Dr Antreas Kalli and I will act as a co-supervisor.
My research investigates membrane protein and lipid assembly, with a focus on the specialized “light-harvesting” membranes which are involved in photosynthesis. We wish to understand, mimic and control the organization of membranes, inspired by the “light-harvesting” membranes found within plants (chloroplasts) and photosynthetic bacteria. My group takes a multi-disciplinary approach combining aspects of surface chemistry, nano/micro fabrication, protein biochemistry, spectroscopy and various microscopies.
Biophysics of natural “light-harvesting” membranes of photosynthesis:
A major goal is to understand the role of plant Light-Harvesting Complex II (LHCII) the process of photoprotection. Photosynthetic “light-harvesting” membranes contain organized domains of membrane proteins which work together as a coordinated network for energy trapping. The plant protein LHCII acts as the major antenna protein for plants, and is possibly the most abundant membrane protein in the world. It has a critical role in safely dissipating energy when light intensity is too high (e.g., on a cold, sunny day). We are studying the molecular mechanism of this photoprotective process (called “nonphotochemical quenching”) by performing experiments and collaborating with theoreticians. We also have a longstanding interest in the LH membranes from purple bacteria and “chlorosome” antennae of green bacteria.
Model biomembranes, artificial photosynthesis and nanotechnology:
Another goal is the development of novel nanocomposites for energy transfer. Purified LH proteins, natural lipids, synthetic lipids, quantum dots, polymers and other materials are used as building blocks to generate model protein/lipid systems. Using lipid bilayers as a platform, we have shown that we can interface Light Harvesting proteins with a range of different nanomaterials, to study their function and to change (possibly “enhance”) the natural proteins. Relatedly, we are interested in model lipid membranes as a platform to study lipid biophysics and protein function. By mimicking the natural stacked membrane but attaching them to glass or mica surfaces, these model membranes are biologically relevant and also amenable to characterization by advanced microscopy.
Advanced microscopy and spectroscopy of various biophysical samples:
We are interested in using Atomic Force Microscopy (AFM) to understand natural and synthetic membranes and protein arrangements in collaborations with others. AFM has excellent signal-to-noise and can image soft biological samples to sub-nanometre spatial resolution. For example we can observe the arrangement of hundreds of membrane proteins without the need for averaging. We are also interested in time-resolved fluorescence spectroscopy and fluorescence microscopy (TCSPC and FLIM) to explore the photophysical properties of any interesting biological or nanophotonic materials.<h4>Research projects</h4> <p>Any research projects I'm currently working on will be listed below. Our list of all <a href="https://eps.leeds.ac.uk/dir/research-projects">research projects</a> allows you to view and search the full list of projects in the faculty.</p>
- PhD, Biochemistry and Microbiology
- BSc First Class, Biochemistry and Microbiology
- Institute of Physics (IOP)
- International Society of Photosynthesis Research (ISPR)
- British Biophysical Society
- Biophysical Society (USA)
Research groups and institutes
- Molecular and Nanoscale Physics
Current postgraduate researchers
<li><a href="//phd.leeds.ac.uk/project/1494-revealing-the-mechanism-of-photoprotection-in-light-harvesting-proteins-using-novel-nanotechnology-and-advanced-time-resolved-fluorescence-microscopy">Revealing the mechanism of photoprotection in light-harvesting proteins using novel nanotechnology and advanced time-resolved fluorescence microscopy</a></li>