Jenny Zhang
@biophotoelectro.bsky.social
41 followers
13 following
5 posts
https://www.ch.cam.ac.uk/group/zhang
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Reposted by Jenny Zhang
ReisnerLab
@reisnerlab.bsky.social
· Jul 26
Cambridge to Lead €4M EU-Funded Sunlight-to-Food Technology Project with European Partners | Yusuf Hamied Department of Chemistry
The Yusuf Department of Chemistry at the University of Cambridge is proud to announce its leadership of a groundbreaking €4 million innovation grant awarded by the European Innovation Council (EIC) Pa...
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Jenny Zhang
@biophotoelectro.bsky.social
· Jul 25
Jenny Zhang
@biophotoelectro.bsky.social
· Jul 25
Dissecting Bioelectrical Networks in Photosynthetic Membranes with Electrochemistry
Photosynthetic membranes contain complex networks of redox proteins and molecules, which direct electrons along various energy-to-chemical interconversion reactions important for sustaining life on Earth. Analyzing and disentangling the mechanisms, regulation, and interdependencies of these electron transfer pathways is extremely difficult, owing to the large number of interacting components in the native membrane environment. While electrochemistry is well established for studying electron transfer in purified proteins, it has proved difficult to wire into proteins within their native membrane environments and even harder to probe on a systems-level the electron transfer networks they are entangled within. Here, we show how photosynthetic membranes from cyanobacteria can be wired to electrodes to access their complex electron transfer networks. Measurements of native membranes with structured electrodes revealed distinctive electrochemical signatures, enabling analysis from the scale of individual proteins to entire biochemical pathways as well as their interplay. This includes measurements of overlapping photosynthetic and respiratory pathways, the redox activities of membrane-bound quinones, along with validation using in operando spectroscopic measurements. Importantly, we further demonstrated extraction of electrons from native membrane-bound Photosystem I at −600 mV versus SHE, which is ∼1 V more negative than from purified photosystems. This finding opens up opportunities for biotechnologies for solar electricity, fuel, and chemical generation. We foresee this electrochemical method being adapted to analyze other photosynthetic and nonphotosynthetic membranes, as well as aiding the development of new biocatalytic, biohybrid, and biomimetic systems.
pubs.acs.org
Jenny Zhang
@biophotoelectro.bsky.social
· Mar 15