Traditional quantum dot synthesis techniques rely on the separation of nucleation and growth to control nanocrystal size. Herein we demonstrate that similar control can be achieved through the continuous generation of reactive precursors throughout synthesis.
a This work demonstrates a bioenabled fully aqueous phase and room temperature route to the synthesis of CuInS2/ZnS core/shell quantum confined nanocrystals conjugated to IgG antibodies and used for fluorescent tagging of THP-1 leukemia cells. This elegant, straightforward and green approach avoids the use of solvents, high temperatures and the necessity to phase transfer the nanocrystals prior to appli-cation.Non-toxic CuInS2, (CuInZn)S2, and CuInS2/ZnS core/shell quantum confined nanocrystals are synthesized via a biomineralization process based on a single recombinant cystathionine γ-lyase (CSE) enzyme. First, soluble In-S complexes are formed from indium acetate and H2S generated by CSE, which are then stabilized by L-cysteine in solution. The subsequent addition of copper, or both copper and zinc, precursors then results in the immediate formation of CuInS2 or (CuInZn)S2 quantum dots. Shell growth is realized through subsequent introduction of Zn acetate to the preformed core nanocrystals. The size and optical properties of the nanocrystals are tuned by adjusting the indium precursor concentration and initial incubation period. CuInS2/ZnS core/shell particles are conjugated to IgG antibodies using EDC/NHS crosslinkers and then applied in the bioimaging of THP-1 cells. Cytotoxicity tests confirm that CuInS2/ ZnS core/shell quantum dots do not cause cell death during bioimaging. Thus, this biomineralization enabled approach provides a facile, low temperature route for the fully aqueous synthesis of non-toxic CuInS2/ZnS quantum dots, which are ideal for use in bioimaging applications.
Cryptophyte algae
are well-known for their ability to survive under
low light conditions using their auxiliary light harvesting antennas,
phycobiliproteins. Mainly acting to absorb light where chlorophyll
cannot (500–650 nm), phycobiliproteins also play an instrumental
role in helping cryptophyte algae respond to changes in light intensity
through the process of photoacclimation. Until recently, photoacclimation
in cryptophyte algae was only observed as a change in the cellular
concentration of phycobiliproteins; however, an additional photoacclimation
response was recently discovered that causes shifts in the phycobiliprotein
absorbance peaks following growth under red, blue, or green light.
Here, we reproduce this newly identified photoacclimation response
in two species of cryptophyte algae and elucidate the origin of the
response on the protein level. We compare isolated native and photoacclimated
phycobiliproteins for these two species using spectroscopy and mass
spectrometry, and we report the X-ray structures of each phycobiliprotein
and the corresponding photoacclimated complex. We find that neither
the protein sequences nor the protein structures are modified by photoacclimation.
We conclude that cryptophyte algae change one chromophore in the phycobiliprotein
β subunits in response to changes in the spectral quality of
light. Ultrafast pump–probe spectroscopy shows that the energy
transfer is weakly affected by photoacclimation.
De novo proteins constructed from novel amino acid sequences are distinct from proteins that evolved in nature. Construct K (ConK) is a binary-patterned de novo designed protein that rescues
Escherichia coli
from otherwise toxic concentrations of copper. ConK was recently found to bind the cofactor PLP (pyridoxal phosphate, the active form of vitamin B
6
). Here, we show that ConK catalyzes the desulfurization of cysteine to H
2
S, which can be used to synthesize CdS nanocrystals in solution. The CdS nanocrystals are approximately 3 nm, as measured by transmission electron microscope, with optical properties similar to those seen in chemically synthesized quantum dots. The CdS nanocrystals synthesized using ConK have slower growth rates and a different growth mechanism than those synthesized using natural biomineralization pathways. The slower growth rate yields CdS nanocrystals with two desirable properties not observed during biomineralization using natural proteins. First, CdS nanocrystals are predominantly of the zinc blende crystal phase; this is in stark contrast to natural biomineralization routes that produce a mixture of zinc blende and wurtzite phase CdS. Second, in contrast to the growth and eventual precipitation observed in natural biomineralization systems, the CdS nanocrystals produced by ConK stabilize at a final size. Future optimization of CdS nanocrystal growth using ConK—or other de novo proteins—may help to overcome the limits on nanocrystal quality typically observed from natural biomineralization by enabling the synthesis of more stable, high-quality quantum dots at room temperature.
Cryptophyte algae are well known for their ability to survive under low light conditions through the use of their auxiliary light harvesting antennas, phycobiliproteins. Mainly acting to absorb light where chlorophyll cannot (500-650 nm), phycobiliproteins also play an instrumental role in helping cryptophyte algae respond to changes in light intensity through the process of photoacclimation. Until recently, photoacclimation in cryptophyte algae was only observed as a change in the cellular concentration of phycobiliproteins; however, an additional photoacclimation response was recently discovered that causes shifts in the phycobiliprotein absorbance peaks following growth under red, blue, or green light. Here, we reproduce this newly identified photoacclimation response in two other species of cryptophyte algae, P. sulcata and H. pacifica, and elucidate the origin of the response on the protein level. We compare isolated native and photoacclimated phycobiliproteins for these two species using spectroscopy and mass spectrometry, and we report the x-ray structures of the PC577 light harvesting complex and corresponding photoacclimated complex. We find that neither the protein sequences, nor the protein structures are modified by photoacclimation. We conclude that cryptophyte algae change a chromophore in one site of their phycobiliprotein beta-subunits as part of the photoacclimation response to changes in the spectral quality of light. Ultrafast pump-probe spectroscopy shows that the energy transfer is weakly affected by the photoacclimation.
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