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The Big Picture

Page 44

by Carroll, Sean M.


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  end is content in the presence of water, while the other wants to avoid it

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  entirely.

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  The lipid’s search for contentment is a metaphorical way of talking

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  about the fact that the system evolves so as to minimize free energy. En-

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  tropy increases, which suggests to us a certain emergent vocabulary, in

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  which the molecules “want” to find a state with low free energy. The arrow

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  of time leads us to speak a language of purpose and desire, even though

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  we’re only talking about molecules obeying the laws of physics.

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  The one thing that the hydrophobic carbon tails can do is to seek com-

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  fort in the company of their own kind. The lipids can line up next to one

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  another, so that their tails are all surrounded by other, equally hydrophobic

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  compatriots, rather than by water. There are a few different ways this can

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  happen. The simplest is for the lipids to form a little ball, called a micel e, 18

  with the hydrophilic heads on the outer surface, exposed to water, while the

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  hydrophobic chains are bundled up with one another.

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  Fatty Acid

  Phospholipid

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  Hydrophilic

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  Head

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  Hydrophobic

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  Hydrocarbon

  Micelle

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  Tail

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  Bilayer

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  There is another option: a bilayer— two sheets of lipids, each one of

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  which has the hydrophilic heads pointing in the same direction, with the

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  hydrophobic tails of the two sheets clinging together. That way the heads

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  get to enjoy the water they seek out, while the tails are completely shielded

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  from it.

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  In an aqueous ( water- containing) solution, lipids will spontaneously or-

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  ganize themselves into one of these types of structures. Which one depends

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  on the circumstances: on what kind of lipid we’re dealing with, and on

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  other properties of the solution, especially whether it is more acidic (likes

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  to give away protons and accept electrons) or alkaline (the opposite).

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  Examples of lipids include fatty acids, which are relatively simple, and

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  phospholipids, which are a bit more complicated. Fatty acids are every-

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  where in biochemistry— they are one of the fuel sources that mitochondria

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  can use to make ATP, for example. Phospholipids consist of two fatty acids

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  joined together by a phosphate group (a compound of phosphorous, carbon,

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  oxygen, nitrogen, and hydrogen).

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  The cellular membranes in organisms living on Earth today are made

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  from bilayers of phospholipids. These molecules very naturally self- organize

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  into bilayers, but not into micelles, because their double tails are too thick

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  to easily fit into the ball- like micelle configuration. The bilayer membranes

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  then fold into themselves to form spherical enclosures, known as vesicles.

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  That’s the easiest part of assembling a cell.

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  One problem with phospholipids, as far as the origin of life is concerned, is

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  that the bilayers they construct are just too good at their job. They are fairly

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  impenetrable, with only water and some other small molecules able to pass

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  from one side to another. It therefore seems likely that the earliest form of

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  cellular membranes were actually made of fatty acids rather than phospho-

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  lipids. Once they are put in place, evolution can set about improving them.

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  Fatty acids can self- assemble into bilayers, but only under the right con-

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  ditions. In highly alkaline solutions, fatty acids prefer to form micelles; in

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  highly acidic conditions, they glom together into big oily drops. At inter-

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  mediate levels of acidity, their favorite configuration is a bilayer. It’s a phase

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  transition, governed by the acidity of the surrounding medium.

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  These bilayers of fatty acids don’t relax into long two- dimensional

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  sheets, like a piece of paper. Rather, they quickly pinch off and form little

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  spheres. That’s the configuration with the lowest free energy in that envi-

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  ronment. It’s another manifestation of how, rather than smooshing every-

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  thing into featureless goo, the second law helps create the kind of organized

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  structures that are useful for life.

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  Fatty acids are relatively simple molecules, so it wouldn’t be hard to find

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  them in appropriate environments on the prebiotic Earth. What’s more, the

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  membranes they form are more permeable than those made of phospholip-

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  ids. That’s good news for early life. In a mature organism, you don’t want

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  chemicals leaking willy- nilly into and out of your cell; embedded in the

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  membranes are very specific structures (like ATP synthase) that guide nu-

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  trients and energy sources in and out as appropriate. Early on, before such

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  dedicated mechanisms have evolved, what you’re looking for is some-

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  thing that can do a fairly good job of compartmentalizing the chemical

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  precursors of life, but not such a good job that they are isolated from the

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  outside world and essentially choked to death. Fatty acids seem just right

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  for the task.

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  •

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  From the perspective of a poetic naturalist, one of the most interesting fea-

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  tures of spontaneous compartmentalization is how it lends itself readily to

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  an emergent description of the system. Without compartments and mem-

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  branes, we’re faced with a soupy mess of compounds, energy sources, and

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  reactions. Once a boundary forms between different kinds of stuff, we can

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  readily talk about the “object” (inside the boundary) and its environment

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  (everything outside). The boundary— whether it’s literally a cell membrane,

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  or the skin or exoskeleton of a multicellular organism— both helps the

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  structure take advantage of the free energy around it and helps us talk

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  about it in useful, computationally efficient ways.

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  Karl Friston, a British neuroscientist, has suggested that the function of

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  biological membranes can be understood in terms of a Markov blanket, a

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  term coined by statistician Judea Pearl in the context of machine learning.

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  Imagine we have a network: a collection of “nodes” connected by lines. A

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  “Bayesian network” is a graph formed from nodes that can send, receive,

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  and process information, like computers on the Internet or neurons in a

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  brain. If we pick out any one node, its Markov blanket consists of all the

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  nodes that can directly influence it (its “parents”), plus all the nodes it can

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  directly influence (its “children”), plus all the nodes that can also influence

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  its children (its “spouses,” of which there may be many).

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  This complicated- sounding construction captures a simple idea: given

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  some part of the network, the Markov blanket captures everything

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  you need to know about its input and output. There may be an enormous

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  number of possible internal states of the nodes, but all that matters for the

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  operation of the network is what gets filtered through the Markov blanket.

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  A cell membrane, argues Friston, can be thought of as a Markov blan-

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  ket. Many intricate processes go on inside the cell, and many things are

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  happening all the time in the environment outside. But communication

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  between the two is mediated through the cell membrane. Under these con-

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  ditions, the system evolves toward a configuration in which the cell mem-

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  brane is robust— it maintains its configuration, even in the presence of

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  ( not- too- large) perturbations from inside or out.

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  External

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  Environment

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  Markov

  Internal

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  Blanket

  States

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  Stimuli & Responses

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  This theory was originally developed not for individual cells but as a

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  way of thinking about how brains interact with the outside world. Our

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  brains construct models of their surroundings, with the goal of not being

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  surprised very often by new information. That process is precisely Bayesian

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  reasoning— subconsciously, the brain carries with it a set of possible things

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  that could happen next, and updates the likelihood of each of them as new

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  data comes in. It is interesting that the same mathematical framework

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  S P O n t A n E Ou S OR g A n I z A t I O n

  might apply to systems on the level of individual cells. Keeping the cell

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  membrane intact and robust turns out to be a kind of Bayesian reasoning.

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  As Friston puts it:

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  The internal states (and their blanket) will appear to engage

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  in active Bayesian inference. In other words, they will appear to

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  model— and act on— their world to preserve their functional

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  and structural integrity, leading to homeostasis [preserving

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  stable internal conditions] and a simple form of autopoiesis

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  [maintaining structure through self- regulation].

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  This is a speculative and new set of ideas, not an established picture of

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  how we should think about the function of cells and membranes. It’s worth

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  remarking on because it shows how the concepts we’ve been talking

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  about— Bayesian reasoning, emergence, the second law— come together to

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  help explain the appearance of complex structures in a world governed by

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  simple, unguided laws of nature.

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  The Origin and Purpose of Life

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  On a crowded flight to a conference in Bozeman, Montana, I was

  reading some research papers on the connection between statistical

  physics and the origin of life. The man sitting next to me glanced

  over at them, curiously. “Oh, yes,” he offered, “I know that work well.”

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  Over the course of a career as a physicist, you run into people who have

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  theories of how the universe works, and are eager to share them with you.

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  Those theories are rarely very promising. Presumably the study of life at-

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  tracts similar numbers of garrulous enthusiasts. But we had a long flight

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  ahead of us; I asked him what his thoughts were on the matter.

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  “That’s easy,” he replied with a nod. “The purpose of life is to hydroge-

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  nate carbon dioxide.”

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  It wasn’t the answer I was expecting. I had been fortuitously seated next

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  to Michael Russell, a geochemist at NASA’s Jet Propulsion Laboratory,

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  close to my own home institution of Caltech. It wasn’t a complete

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  accident— he and I were both traveling to give talks at the same conference.

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  Russell, it turns out, is a leading (if somewhat iconoclastic) figure in the

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  study of life’s origin, and one whose approach is especially physics- friendly.

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  We got along fine.

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  Russell is one of the leaders of a faction in the origin-of-life debates who

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  believes that the first crucial step was the appearance of metabolism. This

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  camp imagines that the crucial event was the appearance of a complex net-

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  work of chemical reactions that took advantage of free energy in the

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  t h E OR I g I n A n d P u R P O S E O F l I F E

  environment of the young Earth, which could then be used to power repli-

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  cation once it began. There is also a replication- first camp, which currently

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  enjoys wider popularity in the community. They tend to think that energy

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  sources are relatively plentiful and unproblematic, and the important leap

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  in the development of life was the synthesis of an information- bearing mol-

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  ecule (presumably RNA, ribonucleic acid) that could duplicate itself and

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  pass down its genetic information.

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  We won’t be adjudicating this disagreement: these are hard questions to

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  which we simply don’t yet know the answers. But they are not hopeless

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  questions. Progress toward understanding abiogenesis has been made on

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  multiple fronts, both theoretically and experimentally. Whatever order me-

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  tabolism and replication appeared in, they are both necessary, and part of

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  the scientific fun will be in figuring out how all the ingredients fit together

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  into the final recipe.

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  •

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  If you want to understand how life began, it makes sense to begin by look-

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  ing for features that are shared by existing forms of life. One such feature

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  seems to be the proton- motive force involved in chemiosmosis, as we dis-

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  cussed in chapter 30. Cell membranes collect energy from photons or from

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  compounds like sugar, and use that energy to expel electrons outside the

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  cell, leaving an excess of protons inside. The mutual repulsion of the pro-

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  tons creates a force that can be used to do useful things like creating ATP.

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  Where did life ever get that idea from? It’s not exactly the obvious way

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  for a cell to manipulate energy. When the chemiosmotic process was worked

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  out by Peter Mitchell and Jennifer Moyle in the 1960s, they were met with

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  enormous skepticism in the biology community, until the experimental

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  evidence became definitive. The fact that nature finds this technique so

 

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