Highlights of our Work
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The ribosome is one of the largest molecular machines present in
hundreds to thousands of copies in every cell, in charge of synthesizing
every protein in the cell faithfully from genetic instruction. For this
purpose the ribosome "reads" the sequence of bases on so-called
messenger RNA, three bases at a time and depending on the base triple,
the codon, elongates a nascent protein by one of 20 possible amino
acids, avoiding to an impressive degree adding a wrong amino acid. So
far one knew that the reading is done by transfer RNA molecules that
have "foots" which match the possible codons and a "head" that brings
along the associated amino acid. Each amino acid has its transfer RNA,
the transfer RNAs checking if the next codon is "theirs," and if it is
they add the proper amino acid to the nascent protein, elongating it.
But how does the ribosome make the critical decision at the decoding
center, namely if the transfer RNA "foot," the so-called anticodon,
matches the codon? The answer is not known, but a key detail has now
been discovered through a combination of electron microscopy and
molecular dynamics simulation using NAMD,
VMD, and a method called flexible
fitting (MDFF, see the June 2008
highlight). It was known that a third molecular system is involved,
called the elongation factor Tu (EF-Tu), which generates a key signal to the
ribosome and transfer RNA through a chemical reaction. This reaction
involves chemically attacking a substrate of EF-Tu, the molecule
guanosine-triphosphate (GTP), with water, breaking a bond and turning GTP
into guanosine-diphosphate (GDP). The puzzle was that EF-Tu is far away
from the decoding center. The collaboration between experiment and
simulation, reported
here, revealed that "correct recognition" through anticodon-codon
binding opens a gate in the EF-Tu that allows water access to the GTP
inducing the signaling reaction. The finding promises to now establish
how the decision at the decoding center is made and how an "open sesame"
order is transmitted to EF-Tu. More on our ribosome website.