We know that the formation of the universe from nothing was impossible.
We know that spontaneous generation of life was and is impossible.
We have established that evolution itself is impossible.
But what if all three of these assumptions were wrong? What if everything appeared out of nothing, for no reason, and formed itself into life against impossible odds, and evolved into multiple magnificent and self replicating organisms. What then?
Even then evolution is impossible.
Why? Because Proteins have shapes. Proteins are fascinating, complicated, 3 dimensional molecules that function as a result of their shape. The basic shape of the protein allows it to present a particular molecule, or reactive agent, at a particular 3 dimensional site, exposed in such a way that it interacts, usually somewhat like a lock and key, with another protein or membrane in the cell so that a chemical process is either turned on or off (in the case of enzymes), or a portion of the cell is built. Douglas Axe showed evolution to be impossible when “He provided empirical backing for this conclusion from experimental research he earlier published in the Journal of Molecular Biology, finding that only one in 1074 amino-acid sequences yields functional protein folds.”(1)
If one alters the DNA by some mechanism (radiation for instance) and the DNA now produces a slightly different protein, then the 3D structure of the protein is altered, and it does not become a new functional protein with a different and “better” use in the cell or the organism. It becomes a useless, broken, messy, senseless system, producing meaningless and often damaging or fatal proteins. (Lou Gehrigs, Alzheimers, Cystic Fibrosis). For example, according to Cystic Fibrosis News today, “The development of CF results from a misfolded or improperly functioning protein known as the cystic fibrosis conductance regulator (CFTR).”(2)
There are, on the other hand, NO (none, nada, zero) examples of enzymes or proteins which have been altered as a result of genetic damage to form a new, improved, or more functional state. The oft cited example of bacterial resistance to antibiotics is NOT such an example. According to Munita and Arias in Mechanisms of Antibiotic Resistance, “Classically, bacteria acquire external genetic material through three main strategies, i) transformation (incorporation of naked DNA), ii) transduction (phage mediated) and, iii) conjugation (bacterial “sex”).” (3) In each case the genetic material ALREADY EXISTED and no new protein or altered gene was required. In fact, the path to antibiotic resistance involves a loss of genetic material from damaged DNA. The bacterium is no longer as healthy and effective and rapidly growing as it was before, but it has a side benefit of being resistant to a particular antibiotic.
Isaiah 45:18 For thus saith the Lord that created the heavens; God himself that formed the earth and made it; he hath established it, he created it not in vain, he formed it to be inhabited: I am the Lord; and there is none else.
(2) Stephen Shannon, Cystic Fibrosis News Today, March 12, 2015.
(3) Nancy Darrall PhD, in six days, Master Books, pp. 190-193.
(4) Munita, J and Arias C., /www.ncbi.nlm.nih.gov/pmc/articles/PMC4888801/
(For more see also “What is Natural Selection” and “Natural Selection is Magic”)