The first 21 years of my life were spent
in Provo, Utah, then a city of about 15,000 people, beautifully
situated at the foot of the Wasatch Mountains. Hardy Mormon
pioneers had settled the area only 70 years before my birth in
1918. Provo was a well-designed city with stable neighbourhoods,
a pride in its past and a spirit of unbounded opportunity. The
geographical isolation and lack of television made world
happenings and problems seem remote.
My father, Dell Delos Boyer, born in 1879 in Springville, Utah,
came from the Pennsylvania Boyers, who in turn came from an
earlier Bayer ancestry in what is now Holland and Germany. A
small portion of my Boyer DNA has been traced to John Alden,
famous as a Mayflower pilgrim who wooed for another and won for
himself. Dad's education, at what was then the Brigham Young
Academy, was delayed by the ill health he had endured in much of
his youth. Through his ambition, and the sacrifices of his
family, he acquired training in Los Angeles to become an
osteopathic physician. He served humanity well. More by example
than by word, my father taught me logical reasoning, compassion,
love of others, honesty, and discipline applied with
understanding. He also taught me such skills such as pitching
horseshoes and growing vegetables. Dad loved to travel. Family
trips to Yellowstone and to what are now national parks in
Southern Utah, driving the primitive roads and cars of that day,
were real adventures. Father became a widower when the youngest
of my five siblings was only eight. Fifteen years later he
married another fine woman. They shared many happy times, and she
cared for him during a long illness as he died from prostate
cancer at the age of 82. Prostate cancer also took the life of my
only brother when he was 76. If our society continues to support
basic research on how living organisms function, it is likely
that my great grandchildren will be spared the agony of losing
family members to most types of cancer.
Recently I scanned notes on a diary that my mother, Grace Guymon,
wrote in her late teens, when living near Mancos, Colorado. The
Guymons were among the Huguenots who fled religious persecution
in France. My French heritage has been mixed with English and
other nationalities as the Guymons descended. Mother's diary
revealed to me more about her vitality and charm than I
remembered from her later years, which were clouded by Addison's
disease. She died in 1933, at the age of 45, just weeks after my
fifteenth birthday. Discoveries about the adrenal hormones, that
could have saved her life, came too late. Her death contributed
to my later interest in studying biochemistry, an interest that
has not been fulfilled in the sense that my accomplishments
remain more at the basic than the applied level. Mother made a
glorious home environment for my early years. During her long
illness and after her death, all of the children helped with
family chores. One of my less pleasant memories is of getting up
in the middle of the night to use our allotted irrigation time to
water the garden.
The large, gracious home provided by Mother and Dad at 346 North
University Avenue has been replaced by a pizza parlor, although
an inspection a few months ago revealed that the irrigation ditch
for our garden area (now a parking lot) can still be found.
Mother had a talent for home decorating. I often read from a set
of the Book of Knowledge or Harvard Classics while lying
in front of the fireplace, with a mantel designed and decorated
by her. Staring into the glowing coals as a fire dims provided a
wonderful milieu for a youthful imagination. I also remember such
things as picnics in Provo Canyon, and the anticipation that I
might get to lick the dasher after cranking the ice-cream
freezer. My older brother, Roy, and I had a play-fight
relationship. I still carry a scar on my nose from when I plunged
(he pushed me!) through the mirror of the dining room closet. I
am told that I had a bad temper, and remember being banished to
the back hall until civility returned. Perhaps this temper was
later sublimated into drive and tenacity, traits that may have
come in part from my mother.
The great depression of the 1930s left lasting impressions on all
our family. Father's patients became non-paying or often
exchanged farm produce or some labor for medical care. Mother
saved pennies to pay the taxes. The burden of paper routes and
odd jobs to provide my spending money made it painful when my new
Iver Johnson bicycle was stolen. We were encouraged to be
creative. I recall mother's tolerance when she allowed me, at an
early age, to take off the hinges and doors of cupboards if I
would put them back on. My first exposure to chemistry came when
I was given a chemistry set for Christmas. It competed for space
in our basement with a model electric trains and an "Erector"
set. After school the neighborhood yards were filled with shouts
of play; games of "kick-the-can," "run-sheepy-run,"
"steal-the-sticks," as well as marbles, baseball and other
activities. In our back yard we built tree houses, dug
underground tunnels and secret passages, and made a small club
house. The mountains above our house offered other outlets for
adventuresome teenage boys. Days were spent in an abandoned cabin
or sleeping under the sky in the shadow of Provo peak. We even
took cultures of sour dough bread to the mountains and baked
delicious biscuits in an a rusty stove. Mountain hikes instilled
in me a life-long urge to get to the top of any inviting summit
or peak.
Provo public schools were excellent. At Parker Elementary School,
a few blocks from my home, I fell in love with my 3rd grade
teacher, Miss McKay. Students who learned more easily were
allowed to skip a grade, and I entered the new Farrer Junior High
school at a younger age than my classmates. This handicapped me
in two types of sporting events, athletics and courting girls.
Girls did not want to dance with little Paul Boyer; boys were
quite unimpressed with my physique. As I grew my status among
fellows improved. Once I got into a scuffle in gym class, the
instructor had the "combatants" put on boxing gloves, and I gave
more than I received. It wasn't until late high school and early
college that I gained enough size and skill to make me welcome on
intramural basketball teams.
I was one of about 500 students of Provo High School, where the
atmosphere was friendly, and scholarship and activities were
encouraged by both students and faculty. I participated on
debating teams and in student government, and served as senior
class president. I still have a particularly high regard for my
chemistry teacher, Rees Bench. I was pleased when he wrote in my
Yearbook for graduation, "You have proven yourself as a most
outstanding student." I graduated while still 16, and thought
myself quite mature. I wish I had saved a copy of my
valedictorian address. I suspect it may have sparkled with
naivete.
It was always assumed that I would go to college. The Brigham Young
University (BYU) campus was just a few blocks from my home
and tuition was minimal. It was a small college of about 3,500
students, less than a tenth of its present size. As in high
school, I enjoyed social and student government activities.
Friendships abounded. New vistas were opened in a variety of
fields of learning. Chemistry and mathematics seemed logical
studies to emphasize, although I had little concept as to where
they might lead. A painstaking course in qualitative and
quantitative analysis by John Wing gave me an appreciation of the
need for, and beauty of, accurate measurement. However, the
lingering odor of hydrogen sulfide, used for metal identification
and separation, called unwanted attention to me in later classes.
"Prof" Joe Nichol's enthusiasm for general chemistry was superbly
conveyed to his students. Professor Charles Maw excelled in
transferring a knowledge of organic chemistry to his students.
Biochemistry was not included in the curriculum.
Summers I worked as a waiter and managerial assistant at
Pinecrest Inn, in a canyon near Salt Lake City. One summer a
college friend and I lived there in a sheep camp trailer while
managing a string of saddle horses for the guests to use. A
different type of education came when as a member of a medical
corps in the National Guard I spent several weeks in a military
camp in California.
As my senior year progressed several career paths were
considered; employment as a chemist in the mining industry, a
training program in hotel management, the study of osteopathic or
conventional medicine, or some type of graduate training. Little
information was available about the latter possibility; but a few
chemistry majors from BYU had gone on to graduate school. I have
a tendency to be lucky and make the right choices based on
limited information. A notice was posted of a Wisconsin Alumni
Research Foundation (WARF) Scholarship for graduate studies. My
application was approved, and the stage was set for a later phase
of my career.
Before leaving Provo, a most important and fortunate event
occurred. A beautiful and talented brunette coed, with one year
of college to finish, indicated a willingness to marry me. She
came from a large and loving family, impoverished financially by
her father's death when she was 2 years old. She had worked and
charmed her way nearly through college. My savings were limited
and hers were negative. But it was clear that my choice was to
have her join with me in the Wisconsin adventure or take my
chances when I returned a year later. It was an easy decision.
Paul, who had just turned 21, and Lyda Whicker, 20, were married
in my father's home on August 31, 1939. Five days later we left
by train to Wisconsin for my graduate study.
A few months after our arrival our new marriage almost ended. I
was admitted to the student infirmary with diagnosed
appendicitis. Through medical mismanagement my appendix ruptured
and I became deathly ill. Sulfanilamides, discovered a few years
earlier by Domagk, saved my life.
Last summer I read an outstanding book, The Forgotten Plague:
How the Battle Against Tuberculosis Was Won and Lost, by
Frank Ryan. The book gives a stirring account, the first I have
read, of Domagk's research and how he was not allowed to leave
Hitler's Germany to receive the 1939 Nobel Prize.
Fortunately, the Biochemistry Department at the University of Wisconsin in
Madison was outstanding and far ahead of most others in the
country. A new wing on the biochemistry building had recently
been opened. The excitement of vitamins, nutrition and metabolism
permeated the environment. Steenbock had recently patented the
irradiation of milk for enrichment with vitamin D. Elvehjem's
group had discovered that nicotinic acid would cure pellagra.
Petersen's group was identifying and separating bacterial growth
factors. Link's group was isolating and identifying a vitamin K
antagonist from sweet clover. Patents for the use of dicoumarol
as a rat poison and as an anticoagulant sweetened the coffers of
the WARF, the Foundation that supported my scholarship. Among
younger faculty an interest in enzymology and metabolism was
blossoming.
Married graduate students were rare, and the continuing economic
depression made jobs hard to find. But my remarkable wife soon
found a good job, and I settled into graduate studies. During our
Wisconsin years she gained a perspective of art while employed in
Madison's leading art retail outlet. It was years later before
Lyda finished a college degree, became a professional editor at
UCLA, and worked with me on the eighteen-volume series of The
Enzymes. Our contacts in graduate school and through Lyda's
employment gave us life-long friends; one was Henry Lardy, from
South Dakota farm country. He and I were assigned to work under
Professor Paul Phillips. Henry was highly talented, and it was my
good fortune to work along side him. Phillips' main interests
were in reproductive and nutritional problems of farm animals.
Henry developed an egg yolk medium for sperm storage that
revolutionized animal breeding.
We were encouraged by Phillips to explore metabolic and enzyme
interests. I did not realize that it was unusual to be able step
across the hall and attend a symposium on respiratory enzymes in
which such biochemical giants as Otto Meyerhof, Fritz Lipmann, and
Carl Cori
spoke. Evening research discussion groups with keen young faculty
such as Marvin Johnson and Van Potter, centered on enzymes and
metabolism, broadened and sharpened our perspectives. One evening
I presented my and Henry's evidence for the first known
K+ activation of an enzyme, pyruvate kinase. Henry
kept score on the interruptions for questions or discussions-some
35 as I recall. This superb training environment set the base for
my career.
My Ph.D. degree was granted in the spring of 1943, the nation was
at war, and I headed for a war project at Stanford
University. A few weeks after my arrival in California, on my
birthday, July 31, our daughter Gail was born. I became somewhat
more involved in home duties and more deeply in love with
Lyda.
The wartime Committee on Medical Research sponsored a project at
Stanford University on blood plasma proteins, under the direction
of J. Murray Luck, founder of the nonprofit Annual Review of
Biochemistry and other Reviews. Concentrated serum albumin
fractionated from blood plasma was effective in battlefield
treatment of shock. When heated to kill microorganisms and
viruses, the solutions of albumin developed cloudiness from
protein denaturation. The principal goal of our research project
was to find some way to stabilize the solutions so that they
would not show this behavior. Our small group found that acetate
gave some stabilization and butyrate was better. This led to the
discovery that long chain fatty acids would remarkably stabilize
serum albumin to heat denaturation, and would even reverse the
denaturation by heat or concentrated urea solutions. Other
compounds with hydrophobic portions and a negative charge, such
as acetyl tryptophan, were also effective. Our stabilization
method was quickly adopted and is still in use. From the Stanford
studies I gained experience with proteins and a growing respect
for the beauty of their structures.
In marked contrast to the University of Wisconsin, Biochemistry
was hardly visible at Stanford in 1945, consisting of only two
professors in the chemistry department. The war project at
Stanford was essentially completed, and I accepted an offer of an
Assistant Professorship at the University of Minnesota, which had a good
biochemistry department. But my local War Draft Board in Provo,
Utah, had other plans and I became a member of the U.S. Navy. The
Navy did not know what to do with me, the war with Japan was
nearly over, and I became what is likely the only seaman
second-class that has had a nearly private laboratory at the Navy
Medical Research Institute in Bethesda, Maryland. In less than a
year I returned to civilian life. In the spring of 1946 I, my
wife, and now two daughters, Gail and Hali, became Minnesotans.
But I had unknowingly acquired a latent California virus to be
expressed years later.
Minnesota has generally competent and honest public officials,
good support of the schools and cultural amenities, and an
excellent state university. It was a fine place to rear a family,
and soon our third child, Douglas, was born. A golden era for
biochemistry was just starting. The NIH and NSF research grants were expanding at a rate equal
to, or even ahead, of the growing number of meritorious
applications. The G.I. bill provided financial support that
brought excellent and mature graduate students to campus. New
insights into metabolism, enzyme action, and protein structure
and function were being rapidly acquired.
Housing was almost unavailable in the post war years. Initially
we coped with an isolated, rat-infested farm house. In 1950,
after my academic competence seemed satisfactorily established,
we built a home not far from the St. Paul campus where the
Department of Biochemistry was located. I served as contractor,
plumber, electrician, finish carpenter etc. My warm memories of
this home include looking at a sparkling, snow-covered landscape,
while seated at the desk in the bedroom corner that served as my
study, and struggling with the interpretation of some puzzling
isotope exchanges accompanying an enzyme catalysis. The
understanding that developed was rewarding and perhaps one of my
best intellectual efforts. However, it did not seem that the
approach would give answers to major problems.
During my early years at Minnesota I conducted an evening enzyme
seminar. One participant in our lively discussions was a
promising graduate student from another department, Bo Malmstrom,
who became a renowned scientist in his field, and is now a
retired professor from the University of Göteborg. In 1952
my family spent a memorable summer at the Woods Hole Marine
Biological Laboratories on Cape Cod. A sabbatical period on a
Guggenheim Fellowship in Sweden in 1955 was especially rewarding.
There I did research at both the Wenner-Gren Institute of the
University of
Stockholm with Olov Lindberg and Lars Ernster, and at the
Nobel Medical Institute, working with
Hugo Theorell's
group. Professor Theorell received a Nobel Prize that year,
exposing us to the splendor and formality of the Nobel
festivities.
Along the way, I was gratified to receive the Award in Enzyme
Chemistry of the American Chemical Society in 1955. In 1959-60 I
served as Chairman of the Biochemistry Section of the American Chemical
Society. In 1956 I accepted a Hill Foundation Professorship
and moved to the medical school campus of the University of
Minnesota in Minneapolis. Much of my group's research was on
enzymes other than the ATP synthase. But solving how oxidative
phosphorylation occurred remained one the most challenging
problems of biochemistry, and I could not resist its siren call.
Mildred Cohn reported that mitochondria doing oxidative
phosphorylation catalyzed an exchange of the phosphate and water
oxygens, an intriguing capacity. An able physicist and a pioneer
in mass spectrometry, Alfred Nier, made gaseous 18O
and facilities available to me, and some experiments were run
using this heavy isotope of oxygen. However, much of our effort
over several years was directed toward attempting to detect a
possible phosphorylated intermediate in ATP (adenosine
triphosphate) synthesis using 32P as a probe. The
combined efforts of some excellent graduate students and
postdocs, most of whom went on to rewarding academic careers,
culminated in the discovery of a new type of phosphorylated
protein, a catalytic intermediate in ATP formation with a
phosphoryl group attached to a histidine residue.
By then, time and queries had stimulated the latent California
virus. Change was underway. In the summer of 1963, I and a group
of graduate students and postdocs who came with me, activated
laboratories in the new wing of the chemistry building at the
University of
California in Los Angeles (UCLA), located on a beautiful
campus at the foot of the Santa Monica mountains. We soon found
that the enzyme-bound phosphohistidine we had discovered was an
intermediate in the substrate level phosphorylation of the citric
acid cycle. It was not a key to oxidative phosphorylation. The
experience reminds me of a favorite saying: Most of the yield
from research efforts comes from the coal that is mined while
looking for diamonds.
In 1965 I accepted the Directorship of a newly created Molecular
Biology Institute (MBI) at UCLA, in part because of my
disappointment that oxidative phosphorylation had resisted our
efforts. A building that was promised failed to materialize, but
through luck and persistence adequate funds were obtained, partly
from private resources, and promising faculty were recruited. The
objective was to promote basic research on how living cells
function at the molecular level. I believe the best research is
accomplished by a faculty member with a small group of graduate
students and postdocs, who freely design, competently conduct and
intensely evaluate experiments. To spend time with such a group I
soon found ways to reduce my administrative chores. Probes of
oxidative phosphorylation continued, and, as 1971 approached, we
hit pay dirt. We recognized the first main postulate of what was
to become the binding change mechanism for ATP synthesis, namely
that energy input was not used primarily to form the ATP
molecule, but to promote the release of an already formed and
tightly bound ATP.
In the following decade, the other two main concepts of the
mechanism were revealed, namely that the three catalytic sites
participate sequentially and cooperatively, and that our, and
other, data could be best explained by what was termed a
rotational catalysis. These previously unrecognized concepts in
enzymology provided motivation and excitement within my research
group. Richard Cross, a postdoctoral fellow trained with Jui Wang
at Yale,
capably probed tightly bound ATP. Jan Rosing, a gifted
experimentalist from Bill Slater's group in Amsterdam, and Celik
Kayalar, an intelligent, innovative graduate student from Turkey,
formed a productive pair that unveiled essential facets of
cooperative catalysis. David Hackney, a postdoc from Dan
Koshland's stable of budding scientists at Berkeley, was an
intellectual leader in our 18O experimentation that
led to rotational catalysis. Dan Smith, Michael Gresser, Linda
Smith, and Chana Vinkler (from Israel) as postdocs, and Lee
Hutton, Gary Rosen and Glenda Choate as graduate students,
established the participation of bound intermediates in rapid
mixing and quenching experiments, and conducted 18O
exchange experiments that clarified and supported our mechanistic
postulates.
In ensuing years, other aspects of the complex ATP synthase were
explored that solidified our feeling that the binding change
mechanism was likely valid and general, and promoted its
acceptance in the field. I will resist telling you here about the
number, properties, and function of the six nucleotide binding
sites, of the probes that agreed with rotational catalysis, of
the unraveling of the complex Mg2+ and ADP inhibition,
of the generality of the mechanism and other synthase properties
revealed by studies with chloroplasts, E. coli, and
Kagawa's thermophilic bacterium. It was a pleasure to work on
such problems with Teri Melese, a postdoc who excelled in
enthusiasm as well as capability, and Zhixiong Xue, an
exceptional graduate student that I first met while leading a
biochemical delegation to China, with Raj Kandpal a scholarly
postdoc from India, with the productive postdocs John Wise (from
Alan Senior's lab) and Rick Feldman (from David Sigman's lab),
with Janet Wood during her sabbatical, and with June-Mei Zhou and
Ziyun Du (on leave from Academia Sinica laboratories in China) as
well as Dan Wu, Steven Stroop, and Karen Guerrero as graduate
students. Special mention should be made of three excellent
Russian researchers, Vladimir Kasho, Yakov Milgrom and Marat
Murataliev, from the laboratory of Vladimir Skulachev, a
respected leader in bioenergetics. With the latter two I am now
writing what will likely be my last paper reporting research
results. Other welcome postdocs, visitors, and graduate students
at UCLA worked with other problems, including the
Na+,K+ -ATPase that Skou first isolated,
and the related Ca++ transporting ATPase of the
sarcoplasmic reticulum. During these active years it was a
pleasure to receive peer recognition in the form of the Rose
Award of the American Society for Biochemistry and Molecular
Biology, the preeminent society in my field (I served as its
President many years earlier).
An unexpected benefit of my career in biochemistry has been
travel. The information exchanged and gained at scientific
conferences and visits has been tremendously important for
progress in my laboratory. My travelophilic wife and I thoroughly
enjoyed being guests of the Australian and South African
biochemical societies while visiting their countries. Meetings or
laboratory visits in Japan, Sweden, France, Germany, Russia,
Italy, Wales, Argentina, Iran, and elsewhere gave us a world
perspective. Manuscripts that have to be produced, sometimes a
bit unwillingly, offer the challenge to present speculation and
perspective often not welcome by editors of prestigious journals.
It was in a volume from a conference dedicated to one of the
giants of the bioenergetics field, Efraim Racker, that the
designation "the binding change mechanism" was introduced.
Conferences at the University of Wisconsin provided opportunity
to publish thoughts about rotational catalysis that had not been
enthusiastically endorsed at Gordon Conferences, where
information is exchanged without publication. These travels have
strong scientific justification. They provided the opportunity
for exchange of information, to test new ideas, to gain new
perspective, and to avoid unnecessary experiments. The milieu
encourages innovation and planning, as well as providing a
stimulus and vitality that fosters research progress.
Other events that make up a lifetime continued. Through fortunate
circumstances, Lyda and I obtained a building lot at a price that
a professor could afford, in the hills north of UCLA, overlooking
the city and ocean. The home we built (I was again contractor and
miscellaneous laborer) has served as a focal point for family
activities, and a temporary residence for grandchildren attending
UCLA. The home meant much for my research, as I could readily
move between home and lab, and the ambiance created was
supportive for study and writing.
The study of life processes has given me a deep appreciation for
the marvel of the living cell. The beauty, the design, and the
controls honed by years of evolution, and the ability humans have
to gain more and more understanding of life, the earth and the
universe, are wonderful to contemplate. I firmly believe that our
present and future knowledge of all that we are and what
surrounds us depends on the tools and approaches of science. I
was struck by how well Harold
Kroto, one of last year's Nobelists, presented what are some
of my views in his biographical sketch. As he stated, "I am a
devout atheist--nothing else makes sense to me and I must admit
to being bewildered by those, who in the face of what appears to
be so obvious, still believe in a mystical creator." I wonder if
in the United States we will ever reach the day when the man-made
concept of a God will not appear on our money, and for political
survival must be invoked by those who seek to represent us in our
democracy.
It is disappointing how little the understanding that science
provides seems to have permeated into society as a whole. All too
common attitudes and approaches seem to have progressed little
since the days of Galileo. Religious fundamentalists successfully
oppose the teaching of evolution, and by this decry the teaching
of critical thinking. We humans have a remarkable ability to
blind ourselves to unpleasant facts. This applies not only to
mystical and religious beliefs, but also to long-term
environmental consequences of our actions. If we fail to teach
our children the skills they need to think clearly, they will
march behind whatever guru wears the shiniest cloak. Our
political processes and a host of human interactions are
undermined because many have not learned how to gain a sound
understanding of what they encounter.
The major problem facing humanity is that of the survival of our
selves and our progeny. In my less optimistic moments, I feel
that we will continue to decimate the environment that surrounds
us, even though we know of our folly and of what has happened to
others. Humans could become quite transient occupants of planet
earth. The most important cause of our problem is over
population, which nature, as with other species, will deal with
severely. I hear the cry from capable environmental leaders and
organizations for movement toward sustainable societies. They are
calling for sensible approaches to steer us away from impending
disaster. But their voices remain largely unheard as those with
power, and those misled by religious or nationality concerns,
become immersed in unimportant, self-centered and short range
pursuits.
From Les Prix Nobel. The Nobel Prizes 1997, Editor Tore Frängsmyr, [Nobel Foundation], Stockholm, 1998
This autobiography/biography was written at the time of the award and later published in the book series Les Prix Nobel/Nobel Lectures. The information is sometimes updated with an addendum submitted by the Laureate. To cite this document, always state the source as shown above.
Copyright © The Nobel Foundation 1997