Back in the 'old
days' of Caleb and earlier, we could pretty much describe
the entire organism, and draw out its molecules in a little picture.
But from this point forward, it's going to be much more difficult
to picture the whole, exact organism. We will also need to skip
over many vital parts of the emerging biochemistry, so we can concentrate
on DNA .
It's important to keep in mind that many changes were probably
happening in parallel, as Caleb gradually became Cassius, and as
Cassius gradually became modern life. Small advances in any 'life
like' feature would have increased the speed of further advances
in others. And none of these features could have happened on their
own, without the gradual appearance of the other improvements, at
approximately the same time.
The Membrane
Aside from self-replication, probably the
most momentous thing Cassius could do was to separate itself from
its surroundings, and become a real cell. That probably happened
shortly after Cassius first stumbled upon some genetic chain which
produced enzymes capable of synthesizing phospholipids, terpenes
or other membrane-forming materials.
Those substances are amphiphilic, which means
they contain a polar (water-loving) group
at one end and a hydrophobic (oily)
group at the other. In water, they will form a two-layer film
with the oil on the inside and the polar
groups on the outside (in this illustration,
the circles are the polar, water-loving exterior of the membrane,
and the squiggles
are the hydrophobic, oily interior)).
If there are enough of the amphiphilic molecules,
they will spontaneously form a micelle or
simple cell, which could have surrounded
the main Cassius complex. Being inside a
membrane would have created a portable, concentrated
local soup where Fred and Roscoe could function
properly, not just in specific puddles, but
anywhere .
Any Cassius with a membrane would have synthesized
more efficiently, and also suffer less trouble
from proteolytic enzymes and other soup hazards.
Adding a boundary between a cell and its
surroundings is such a useful improvement
that it would have revolutionized the prebiotic
world, once it developed.
Of course, early versions of Cassius couldn't
just move to the inside of a bubble of lipids
immediately, since they still needed access
to their raw materials in the surrounding
soup. A full lipid layer would prevent most
compounds from diffusing into the cell interior,
and that would eventually starve Cassius.
Since early versions of Cassius were not
yet ready to live inside a cell, they probably
started out by living on or near a lipid
film on some other surface, or they may have
even taken up residence on the outside of
a membrane, for a while, and only later moved
to the interior.
Regardless of its shape, even a simple lipid
layer would have given Cassius a quick selective
advantage, by providing it with a substrate
to anchor its enzymes. Let's take a
look at how that might have worked.
Membrane Proteins
Membranes are very interesting from a chemical
point of view, since they provide a small
strip of oil or other hydrocarbon that is
surrounded by water. One of the first amino
acids in Fred was probably a hydrophobic
(oil loving) molecule and the other was probably
polar (oil repelling), so Fred and other
early proteins would have interacted with
a membrane in some specific ways.
For example, a protein that contained both
polar regions and hydrophobic regions would
take up a specific position within such a
film, with its hydrophobic areas imbedded
in the hydrophobic core of the film, and
its polar parts sticking out.
A protein with a hydrophobic middle and polar
groups at the two ends might 'bridge' the
membrane, and have both ends sticking out
on opposite sides.
Proteins embedded in a membrane have restricted
motion-- they can easily slip sideways
through the film and twirl about their own
axis, but they can't move very much
at right angles to the film, nor rotate in
any direction other than axially. The hydrophobic
attraction between the lipid core and the
hydrophobic amino acids keeps the protein
in a relatively fixed position.
Membrane Positioning
We have already talked about the use of backbone
chains as a way to confine enzymes into a
fixed position, so they can work together
as a supercatalyst. Membranes could also
have served a similar function. Several proteins
might all be imbedded in a film, which would
hold them together rigidly so they could
perform as a supercatalyst.
You might think of a membrane as an extremely
effective way to impose some two-dimensional
order onto a three-dimensional assembly of
free-floating enzymes.
Membrane Pores
Once there were sufficient types of proteins
floating within membranes, some of them may
have formed a 'ring' structure
within a membrane, which would have created
a pore that allowed a connection from one
side to the other. In fact, a single protein
with just the right placement of hydrophobic
and polar amino acids could clump up with
others of its kind within a membrane, and
pierce a hole through to the outside.
With the right types of pores, an advanced
membrane-building Cassius would become a
true cell. As with modern cells, it could
control the chemistry of its local environment
by restricting what went through the pores.
Once that happened, all of its chemistry
could occur within a wrap-around membrane,
with all the advantages it entailed.
Of course, the ideal pores would let in any
useful raw materials from the outside, without
allowing useful cell contents to seep out.
So pore proteins would have been under enormous
selective pressure to improve their skills
at regulating the cell contents.
Membranes and Nathaniel
Once there were membranes to hold in Cassius's
contents, there would have been no particular
need for Nathaniels to hold together the
different proteins and chains.
Of course, some Nathaniel connections may
have still remained in place as a way to
keep various components close to each other
within the cell.
For example, the linkage between Fred and
the various chains (Sofia, Sorrel etc) would
still have provided a selective advantage,
since it would have made protein transcription
happen more easily.
Earlier Membranes
It is possible that phospholipids were present
in the early soup, in which case they may
have formed natural membranes even before
Fred and Sofia came onto the scene . In that
case, much of the molecular evolution that
we have discussed so far may have occurred
within micelles or vesicles (cell-like structures
created from natural membrane materials)
A micelle with a few supercatalysts inside
may have provided the exact right conditions
for early replication chemistry, without
the need for tidal pools or puddles. Of course
such early 'pseudo-cells' would
have only been a temporary, dead-end stage
of cell development, since they had no way
to synthesize more membrane material (at
least not from an enzyme coded from a genetic
script). Any Caleb or Cassius that used natural
phospholipids would have been completely
at the mercy of the natural processes that
formed them locally.
Because of that, the first versions of Cassius
that could synthesize their own membranes
would still have gained an enormous selective
advantage, even if earlier cells had formed
by natural processes, before the first Cassius-synthesized
membrane.
Phenotype and Genotype
An important genetic consequence of the cell
membrane is that it fully enables true Darwinian
selection. By separating the genetic material
from the outside world, the membrane enforces
a complete linkage between a cell's
genotype (Sofia, Sorrel and other genetic
chains) and its phenotype (Fred, Roscoe,
Nathaniel and metabolic proteins).
A mutant Cassius with a new genetic chain
that created an effective new protein would
no longer share any of its genes with surrounding
copies of Cassius . That means that it would
thrive, increase in size, split, and then
spread much more quickly then its less-endowed
neighbors. That could happen anywhere, so
there was no longer any need for isolated
micro-puddles to provide separation and evolution.
In other words, once there were cells, a
new gene could now become established in
the entire population by the 'classic' forces
of natural selection.
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